#reduce urea creatinine level
Explore tagged Tumblr posts
helen0086 · 5 months ago
Text
Progress in the Study of the Protective Effect and Mechanism of C-phycocyanin on Liver Injury
Abstract: C-phycocyanin (C-phycocyanin) is a pigment-containing protein from marine algae that has shown promising results in the treatment of many inflammatory diseases and tumors. C-alpha-cyanobilin is a pigment-containing protein from marine algae that has been shown to be effective in the treatment of various inflammatory diseases and tumors. C-alpha-cyanobilin has a protective effect on various liver diseases, such as drug-induced or toxic substance-induced liver damage, non-alcoholic fatty liver disease, hepatic fibrosis, and hepatic ischemia-reperfusion injury. The protective effect of C-alginin on liver injury is mainly realized through the regulation of signaling pathways such as nuclear factor (NF)-κB, phosphatidylinositol 3-kinase/protein kinase B (PI3K/Akt) and AMP-dependent protein kinase (AMPK), and the inhibition of oxidative stress, etc., and is not toxic to normal cells. Therefore, C-alginin has a broad application prospect as a potential natural hepatoprotective marine active substance. In recent years, the research progress of the protective effect of C-alginin on liver injury and its mechanism is summarized.
Tumblr media
 C-phycocyanin (C-phycocyanin) is a complex protein of cyanobacteria and a natural food protein pigment with pharmacological effects such as antioxidant, anti-inflammatory and anti-tumor effects, as well as fast-acting and low-toxicity, it can be used as a functional food [1-2]. C-Alginin can also enhance immunity and is safe, without causing acute and subacute toxic reactions [3]. Selenium-enriched PC has been shown to have stronger pharmacological effects [4]. Therefore, C-alginate has important research value both as a drug and a functional food, and has become a hot spot in the field of pharmaceutical research [5]. In this paper, we summarize the progress of research on the application and mechanism of C-alginin in liver diseases.
1 Ameliorative effect of C-phycocyanin on liver injury caused by drugs and toxic substances
The liver is the metabolic center of drugs and exogenous toxic substances, and metabolites are prone to liver injury. C-PC can inhibit the synthesis and release of inflammatory factors such as tumor necrosis factor (TNF)-α and interferon-γ, and increase the activities of catalase and superoxide dismutase (SOD), which can inhibit hepatic inflammation and alleviate hepatic injury [3]. It has been found that C-PC can significantly prevent thioacetamide-induced liver injury, significantly reduce the levels of alanine aminotransferase (ALT) and aliquot aminotransferase (AST), shorten the prothrombin time and reduce the hepatic histopathological damage, and improve the survival rate of rats with fulminant hepatic failure [6]. C-alginin also has a good effect on thioacetamide-induced hepatic encephalopathy, which can be seen in the reduction of tryptophan and lipid peroxidation indexes in different regions of the brain, and the enhancement of catalase and glutathione peroxidase activities in rats with fulminant hepatic failure [6].
Another study found that C-alginin not only attenuates the oxidative stress induced by 2-acetylaminofluorene and reduces the generation of reactive oxygen species (ROS) radicals, but also inhibits the phosphorylation of protein kinase B (Akt) and the nuclear translocation of nuclear factor (NF)-κB induced by 2-acetylaminofluorene, thus inhibiting the expression of multidrug resistance genes [7]. Osman et al. [8] also showed that C-alginin could normalize the levels of ALT, AST, catalase, urea, creatinine, SOD and glutathione-s-transferase in the livers of rats poisoned with carbon tetrachloride (CCl4). This result was also verified in human liver cell line (L02) [9]. C-phycocyanin can effectively scavenge ROS and inhibit CCl4-induced lipid peroxidation in rat liver [10], and C-PC can improve the antioxidant defense system and restore the structure of hepatocytes and hepatic enzymes in the liver of gibberellic acid-poisoned albino rats [11]. As a PC chromophore, phycocyanin can also significantly inhibit ROS generation and improve liver injury induced by a variety of drugs and toxic substances [10]. Liu et al. [12] found that phycocyanin showed strong anti-inflammatory effects in a CCl4-induced hepatic injury model in mice, which could significantly reduce the levels of ALT, AST, the expression of TNF-α and cytochrome C, increase the levels of albumin and SOD, and proliferate cytosolic nuclei. It can significantly reduce ALT and AST levels and the expression of TNF-α and cytochrome C, increase albumin levels and the expression of SOD and proliferating cell nuclear antigen, promote hepatocyte regeneration and improve the survival rate of mice with acute liver failure.
Gammoudi et al [13] used response surface method to optimize the extraction process of C-phycocyanin, and obtained high extraction recovery. C-phycocyanin extracted by the optimized method has the ability of scavenging hydroxyl, superoxide anion and nitric oxide radicals as well as the ability of metal chelating, and it has stronger antioxidant effect; C-PC significantly increased the activity of SOD and inhibited the increase of ALT, AST, and bilirubin in cadmium-poisoned rats. C-PC significantly increased the activity of SOD and inhibited the increase of ALT, AST and bilirubin in rats with cadmium poisoning. The above studies show that C-phycocyanin can effectively protect liver injury caused by drugs and toxic substances, and has the efficacy as the basis for drug development.
2 Preventive effect of C-alginin on hepatic fibrosis
Liver fibrosis is an inevitable process in the development of various chronic liver diseases and may be reversed with early and timely treatment. The key to liver fibrosis is the activation of hepatic stellate cells. Previous studies have found that low-dose C-alginin combined with soy isoflavones can inhibit hepatic stellate cell activation by inhibiting the activity of reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase[14], but it is not clear whether C-alginin alone can inhibit the activity of NADPH oxidase. Therefore, the combination of C-algin and soy isoflavones at appropriate doses may have a preventive effect on liver fibrosis in high-risk groups. C-alginin may inhibit the progression of NADPH by suppressing oxidative damage, thereby inhibiting the development of hepatic fibrosis [15].
Epithelial mesenchymal transition (EMT) is one of the key mechanisms contributing to the development of fibrotic diseases. C-alginin inhibits transforming growth factor β1 (TGF-β1)-induced human EMT [16]. Although the effect of C-alginin on EMT in hepatic fibrosis has not been reported, it has been found that C-alginin can reduce pulmonary fibrosis by inhibiting epithelial mesenchymal transition [17]. Another study found that C-alginin could reduce the expression of α-smooth muscle actin (α-SMA) and connective tissue growth factor (CTGF) mRNA in human dermal fibroblasts and alleviate fibrous contracture [18]. The results of these studies also have significance for the inhibition of hepatic fibrosis, and provide a theoretical basis for the further study of C-PC as a potential antifibrotic drug.
3 Protective effect of C-alginin on hepatic ischemia-reperfusion injury
Liver ischemia/reperfusion injury is an important clinicopathophysiological phenomenon. It was found that the addition of two different doses (0.1 g/L and 0.2 g/L) of C-alginin to the Krebs Henseleit preservation solution significantly decreased hepatic ALT, AST and alkaline phosphatase activities, and reduced the rate of lipid peroxidation and malondialdehyde content in an isolated perfused rat liver model, and increased the activities of hepatic glutathione-s-transferase and glutathione peroxidase, as well as sulfhydryl groups in hepatic tissue. On the other hand, it can increase the activities of hepatic glutathione-s-transferase and glutathione peroxidase and the content of sulfhydryl groups in liver tissues, therefore, C-alginin can significantly reduce hepatic ischemia/reperfusion injury as an antioxidant [19]. In isolated perfused mouse livers, it was found that C-alginin significantly reduced the phagocytosis and respiratory burst activity of hepatic macrophages (Kupffer cells), attenuated cytotoxicity and inflammation induced by highly active Kupffer cells, and dose-dependently inhibited carbon phagocytosis and carbon-induced oxygen uptake by perfused livers, and then inhibited the increase of hepatic nitric oxide synthase activity induced by gonadotropins [20]. and thus inhibit the thyroid hormone-induced elevation of hepatic nitric oxide synthase activity [20].
However, C-alginin has a very short half-life in vivo, which limits its application in vivo. It was found that the use of polyethylene glycol-b-(polyglutamic acid-g-polyethyleneimine), a macromolecular material with good drug-carrying capacity and slow-release properties, as a nanocarrier of C-alginin could solve this problem, and the release of C-alginin could be delayed by subcutaneous injection into the abdominal region of rats, which could attenuate islet damage caused by hepatic ischemia/reperfusion and enhance the function of the islets [21]. This study broadens the scope of application of C-alginin in vivo and improves the therapeutic effect of C-alginin.
4 Inhibitory effect of C-alginin on hepatocellular carcinoma
It was found that C-alginin significantly reduced the expression of matrix metalloproteinase (MMP)-2 and MMP-9 and the expression of tissue inhibitor of metalloproteinase 2 (TIMP2) mRNA in human hepatocellular carcinoma cells (HepG2 cells) [22]. C-alginin is a natural photosensitizer, and photodynamic therapy (PDT) mediated by alginin microcystin induced a large accumulation of ROS in HepG2 cells, which promoted mitochondrial damage and cytochrome C release, and led to apoptosis of hepatocellular carcinoma cells [23].
Liu et al. [24] used nanoscale C-alginate particles prepared by lactobionic acid grafting and adriamycin loading to enhance the growth inhibition of HepG2 cells when combined with chemo-PDT, and the C-alginate particles could effectively accumulate and diffuse in tumor multicellular spheres. In vitro and in vivo studies on the effects of selenium-enriched PCs on PDT in hepatocellular carcinoma showed that selenium-enriched PCs could migrate from lysosomes to mitochondria in a time-dependent manner, and that selenium-enriched PCs could induce the death of tumor cells through the generation of free radicals in vivo, increase the activities of antioxidant enzymes in vivo, induce mitochondria-mediated apoptosis, and inhibit autophagy, thus offering a relatively safe pathway to tumor treatment and showing new development perspectives [4]. It can provide a relatively safe way to treat tumors and shows a new development prospect [4].
Lin et al. [25] combined C-phycocyanin with single-walled carbon nanohorns and prepared phycocyanin-functionalized single-walled carbon nanohorn hybrids, which enhanced the photostability of C-phycocyanin and protected the single-walled carbon nanohorns from adsorption of plasma proteins, and synergistically used with PDT and photothermal therapy (PTT) to treat tumors. C-phycocyanin covalently coupled with biosilica and PDT or non-covalently coupled with indocyanine green and PTT on tumor-associated macrophages can also increase the apoptosis rate of tumor cells [26-27]. The development of PDT and PTT synergistic methods for the treatment of cancer has broadened the application of C-PC and enhanced its value in the treatment of hepatocellular carcinoma.
In addition, C-phycocyanin can inhibit the expression of multidrug-resistant genes in HepG2 cells through NF-κB and activated protein-1 (AP-1)-mediated pathways, and C-phycocyanin increases the accumulation of adriamycin in HepG2 cells in a dose-dependent manner, which results in a 5-fold increase in the susceptibility of cells to adriamycin [28]. Even in adriamycin-resistant HepG2 cells, C-PC induced the activation of apoptotic pathways such as cytochrome C and caspase-3 [29], and the results of Prabakaran et al. [30] also confirmed the inhibitory effect of C-PC on the proliferation of HepG2 cells, mediated by the inactivation of BCR-ABL signaling and the downstream PI3K/Akt pathway. mediated by BCR-ABL signaling and inactivation of downstream PI3K/Akt pathway. In addition, C-phycocyanin modifies the mitochondrial membrane potential and promotes apoptosis in cancer cells [30]. Currently, C-phycocyanin is a synergistic molecule with other drugs that have been widely used in the treatment of cancer [31]. The above studies demonstrate that C-phycocyanin has good therapeutic potential in the field of hepatocellular carcinoma.
5 Amelioration of metabolic syndrome and non-alcoholic fatty liver disease by C-phycocyanin
It has been found that C-alginin can reduce ALT and AST levels, decrease ROS production and NF-κB activation, and attenuate hepatic fibrosis in rats induced by high-fat choline-deficient diets, and thus C-alginin has a protective effect on NAFLD rats through anti-inflammatory and antioxidant mechanisms [15].
Another study on the effects of aqueous extract of Spirulina (mainly C-alginin) on NAFLD induced by a high-calorie/high-fat Western diet in C57Bl/6J mice showed that aqueous extract of Spirulina significantly improved glucose tolerance, lowered plasma cholesterol, and increased ursodeoxycholic acid in bile in mice [32]. Kaspi-Chadli et al. Kasbi-Chadli et al. [33] showed that aqueous extract of Spirulina could reduce cholesterol and sphingolipid levels in the liver and aortic cholesterol levels in hamsters fed a high-fat diet by significantly decreasing the expression of hydroxy-3-methylglutaryl-coenzyme A reductase (HMG CoA) gene, a limiting enzyme for cholesterol synthesis, and TGF-β1 gene, and that ursodeoxycholic acid levels in the feces of hamsters fed high-fat diets were increased in the high Spirulina aqueous extract treatment group.
A daily dose of C-alginin-enriched Spirulina can reduce the harmful effects of oxidative stress induced by a diet rich in lipid peroxides [34]. Ma et al. [35] found that C-alginin promoted the phosphorylation of hepatocyte AMP-dependent protein kinase (AMPK) in vivo and ex vivo, and increased the phosphorylation of acetyl coenzyme A carboxylase. In the treatment of NAFLD in mice, C-alginin can improve liver inflammation by up-regulating the expression of phosphorylated AMPK and AMPK-regulated transcription factor peroxisome proliferator-activated receptor α (PPAR-α) and its target gene, CPT1, and by down-regulating the expression of pro-inflammatory factors such as TNF-α and CD36 [35]. This suggests that C-phycocyanin can also improve lipid deposition in the liver through the AMPK pathway.
Endothelial dysfunction is associated with hypertension, atherosclerosis and metabolic syndrome. Studies in animal models of spontaneous hypertension have shown that long-term administration of C-alginin may improve systemic blood pressure in rats by increasing aortic endothelial nitric oxide synthase levels, with a dose-dependent decrease in blood pressure, and thus C-alginin may be useful in preventing endothelial dysfunction-related diseases in the metabolic syndrome [36]. In the offspring of ApoE-deficient mice fed C-alginate during gestation and lactation, male littermates had an elevated hepatic reduced/oxidized glutathione ratio and significantly lower hepatic SOD and glutathione peroxidase gene expression.
C-PC is effective in preventing atherosclerosis in adult hereditary hypercholesterolemic mice [37]. In vitro, C-phycocyanin also improved glucose production and expression of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase (G-6-Pase) in high-glucose-induced insulin-resistant HepG2 cells [38]. C-alginin also increases glucose uptake in high glucose-induced insulin-resistant HepG2 cells through the insulin receptor substrate (IRS)/PI3K/Akt and Sirtuin-1 (SIRT1)/liver kinase B1 (LKB1)/AMPK signaling pathways, activates glycogen synthase, and increases the amount of glycogen [38]. C-phycocyanin can improve blood glucose and fasting serum insulin levels in tetracycline-induced diabetic mice [39]. Therefore, C-phycocyanin can maintain cellular glucose homeostasis by improving insulin resistance in hepatocytes.
6 Hepatoprotective role of C-phycocyanin in other liver diseases
Studies have shown that C-alginin can inhibit total serum cholesterol, triacylglycerol, LDL, ALT, AST, and malondialdehyde levels in mice modeled with alcoholic liver injury, significantly increase SOD levels in the liver, and promote the activation and proliferation of CD4+ T cells, which can have an ameliorative effect on alcoholic liver injury [40]. In addition, C-phycocyanin may enhance the intestinal barrier function, regulate the intestinal flora, reduce the translocation of bacteria and metabolites to the liver, and inhibit the activity of the Toll-like receptor 4 (TLR4)/NF-κB pathway, which may reduce the inflammation of the liver and prevent the occurrence of hepatic fibrosis in mice [41]. In mice with X-ray radiation-induced liver injury, C-phycocyanin can reduce radiation-induced DNA damage and oxidative stress injury by up-regulating the expression of nuclear factor (NF)-E2-related factor 2 (Nrf2) and downstream genes, such as HO-1, and play a hepatoprotective role by enhancing the activities of SOD and glutathione peroxidase [42].
7 Outlook
Liver fibrosis is the common final process of chronic liver diseases, and there is no effective therapeutic drug at present. Although some research progress has been made in the field of traditional Chinese medicine (TCM) on the reversal of liver fibrosis [43], its toxicological effects have not yet been clarified. Although the incidence of viral hepatitis has gradually decreased with the development and popularization of vaccines and antiviral drugs, the incidence of drug-induced liver injury (DILI) and liver diseases such as NAFLD has been increasing year by year with the improvement of people's living conditions [44]. Therefore, there is an urgent need to find drugs or nutrients that can help maintain normal hepatocyte function and effectively inhibit liver inflammation and fibrosis. C-alginin, with its anti-inflammatory, antioxidant, and antitumor effects, as well as good food coloring, has a wide range of applications in both the pharmaceutical and food industries.
References:
[ 1 ] LIU Q, HUANG Y, ZHANG R, et al. Medical aapplication of spirulina platensis derived C-phycocyanin [J].   Evid Based Complement Alternat Med, 2016, 2016: 7803846. doi: 10. 1155/ 2016/7803846.
[2] BRAUNE S , KRÜGER-GENGE A , KAMMERER S , et al. Phycocyanin from Arthrospira platensis as potential anti-cancer drug: review of in vitro and in vivo studies[J]. studies[J]. Life (Basel), 2021, 11 (2): 91. doi:10.3390/life11020091.
[3] GROVER P, BHATNAGAR A, KUMARI N, et al. C-phycocyanin- a novel protein from spirulina platensis- in vivo toxicity, antioxidant and immunomodulatory studies[J].  Saudi J Biol Sci, 2021, 28(3):1853-1859. doi: 10. 1016/j.sjbs.2020.12.037.
[4] LIU Z, FU X, HUANG W, et al. Photodynamic effect and mechanism study of selenium-enriched phycocyanin from spirulina platensis against liver tumours. [J Photochem Photobiol B] J Photochem Photobiol B, 2018, 180: 89-97. doi: 10. 1016/j.jphotobiol.2017.12.020.
[5] JIANG L, WANG Y, YIN Q, et al. Phycocyanin: a potential drug for cancer treatment[J].  J Cancer, 2017, 8 (17): 3416-3429. doi: 10.7150/jca.21058.
[6] SATHYASAIKUMAR K V, SWAPNA I, REDDY P V, et al. Co- administration of C-phycocyanin ameliorates thioacetamide- induced hepatic encephalopathy in Wistar rats[J]. J Neurol Sci, 2007, 252(1):67-75. doi: 10. 1016/j.jns.2006.10.014.
[7] ROY K R , NISHANTH R P , SREKANTH D , et al. C- phycocyanin ameliorates 2-acetylaminofluorene induced oxidative stress and MDR1 expression in the liver of albino mice [J]. of albino mice[J]. Hepatol Res, 2008, 38(5): 511-520. doi: 10.1111/j. 1872-034X. 2007. 00290.x.
[8] OSMAN A, SALAMA A, EMAM MAHMOUD K, et al. Alleviation of carbon tetrachloride-induced hepatocellular damage and oxidative stress in rats by anabaena oryzae phycocyanin[J]. J Food Biochem, 2021, 45(1):e13562. doi:10.1111/jfbc.13562.
[9] OU Y, ZHENG S, LIN L, et al. Protective effect of C-phycocyanin against carbon tetrachloride-induced hepatocyte damage in vitro and in vivo[J]. Chem Biol Interact, 2010, 185(2): 94-100. doi: 10. 1016/j.cbi.2010.03.013.
[10] BHAT V B, MADYASTHA K M. C-phycocyanin: a potent peroxyl radical scavenger in vivo and in vitro [J].  Biochem Biophys Res Commun, 2000, 275(1): 20-25. doi: 10. 1006/bbrc.2000.3270.
[ 11] HUSSEIN M M, ALI H A, AHMED M M. Ameliorative effects of phycocyanin against gibberellic acid induced hepatotoxicity[J]. Pestic Biochem Physiol, 2015, 119: 28-32. doi: 10. 1016/j. pestbp. 2015.02.010.
[ 12]LIU J, ZHANG Q Y, YU L M, et al. Phycocyanobilin accelerates liver regeneration and reduces mortality rate in carbon tetrachloride-induced liver injury mice[J]. World J Gastroenterol, 2015, 21(18):5465-5472. doi:10.3748/wjg.v21.i18.5465.
[13] GAMMOUDI S, ATHMOUNI K, NASRI A, et al. Optimization,  isolation, characterization and hepatoprotective effect of a novel pigment-protein complex (phycocyanin) producing microalga: phormidium versicolorNCC-466 using response surface methodology [J]. versicolorNCC-466 using response surface methodology [J].  Int J Biol Macromol, 2019, 137: 647-656. doi: 10. 1016/j.    ijbiomac.2019.06.237.
[14] MCCARTY M F , BARROSO-ARANDA J , CONTRERAS F. Genistein and phycocyanobilin may prevent hepatic fibrosis by suppressing proliferation and activation of hepatic stellate cells[J]. Med Hypotheses, 2009, 72(3):330-332. doi: 10. 1016/j.mehy.2008. 07.045.
[15]PAK W, TAKAYAMA F, MINE M, et al. Anti-oxidative and anti- inflammatory effects of spirulina on rat model of non-alcoholic steatohepatitis[J]. J Clin Biochem Nutr, 2012, 51(3):227-234. doi:10.3164/jcbn.12-18.
[16] PATTARAYAN D, RAJARAJAN D, SIVANANTHAM A, et al. C- phycocyanin suppresses transforming growth factor- β 1-induced epithelial mesenchymal transition in human epithelial cells [J]. Pharmacol Rep, 2017, 69(3): 426-431. doi: 10. 1016/j. pharep. 2016.12.013.
[ 17]LI C, YU Y, LI W, et al. Phycocyanin attenuates pulmonary fibrosis via the TLR2-MyD88-NF- κB signaling pathway[J].  Sci Rep, 2017, 7 (1): 5843. doi: 10. 1038/s41598-017-06021-5.
[18] AN E, PARK H, LEE A C. Inhibition of fibrotic contraction by C- phycocyanin through modulation of connective tissue growth factor and α-smooth muscle actin expression[J]. Tissue Eng Regen Med, 2016, 13(4):388-395. doi: 10. 1007/s13770-015-0104-5.
[19] GDARA N B, BELGACEM A, KHEMIRI I, et al. Protective effects of phycocyanin on ischemia/reperfusion liver injuries [J]. Biomed Pharmacother, 2018, 102: 196-202. doi: 10. 1016/j. biopha. 2018. 03.025.
[20] REMIREZ D, FERNÁNDEZ V, TAPIA G, et al. Influence of C- phycocyanin on hepatocellular parameters related to liver oxidative stress and kupffer cell functioning[J]. Inflamm Res, 2002, 51(7): 351-356. doi: 10. 1007/pl00000314.
[21] TONG F, TANG X, LIU D. Phycocyanin/PEG-b-(PG-g-PEI) attenuated hepatic ischemia/reperfusion-induced pancreatic islet injury and enlarged islet functionality [J]. Int J Nanomedicine, 2019, 14: 339-351. doi: 10.2147/IJN.S190938.
[22]KUNTE M, DESAI K. The inhibitory effect of C-phycocyanin containing protein extract on human matrix metalloproteinases (MMP-2) and MMP-9 in hepatocellular cancer cell line (HepG2)[J]. and MMP-9) in hepatocellular cancer cell line (HepG2) [J].  Protein J, 2017, 36(3): 186-195. doi: 10. 1007/s10930-017-9707-0.
[23]WANG C Y, WANG X, WANG Y, et al. Photosensitization of phycocyanin extracted from microcystis in human hepatocellular carcinoma cells: implication of mitochondria-dependent apoptosis [J]. J Photochem Photobiol B, 2012, 117: 70-79. doi: 10. 1016/j.  jphotobiol.2012.09.001.
[24]LIU X, DU J, XIE Z, et al. Lactobionic acid-modified phycocyanin nanoparticles loaded with doxorubicin for synergistic chemo- photodynamic therapy[J]. therapy[J]. Int J Biol Macromol, 2021, 186: 206- 217. doi: 10. 1016/j.ijbiomac.2021.07.047.
[25]LIN Z, JIANG B P, LIANG J, et al. Phycocyanin functionalized single-walled carbon nanohorns hybrid for near-infrared light- mediated cancer phototheranostics [J].  Carbon, 2019, 143: 814- 827. doi: 10. 1016/j.carbon.2018.12.011.
[26] PU Y, WEI M, WITKOWSKI A, et al. A hybrid biomaterial of biosilica and C-phycocyanin for enhanced photodynamic effect  towards tumor cells[J]. Biochem Biophys Res Commun, 2020, 533 (3): 573-579. doi: 10. 1016/j.bbrc.2020.09.049.
[27] WAN D H, MA X Y, LIN C, et al. Noncovalent indocyanine green conjugate of C-phycocyanin: preparation and tumor-associated macrophages-targeted photothermal therapeutics[J].   Bioconjug Chem, 2020, 31(5): 1438-1448. doi: 10. 1021/acs. bioconjchem. 0c00139.
[28]NISHANTH R P, RAMAKRISHNA B S, JYOTSNA R G, et al. C- phycocyanin inhibits MDR1 through reactive oxygen species and cyclooxygenase-2 mediated pathways in human hepatocellular carcinoma cell line[J]. Eur J Pharmacol, 2010, 649(1/3):74-83. doi: 10. 1016/j.ejphar.2010.09.011.
[29] ROY K R, ARUNASREE K M, REDDY N P, et al. Alteration of mitochondrial membrane potential by spirulina platensis C- phycocyanin induces apoptosis in the doxorubicinresistant human hepatocellular-carcinoma cell line HepG2[J].  Biotechnol Appl Biochem, 2007, 47 (Pt 3): 159-167. doi: 10. 1042/BA20060206.
[30] PRABAKARAN G, SAMPATHKUMAR P, KAVISRI M, et al. Extraction and characterization of phycocyanin from spirulina platensis and evaluation of its anticancer , antidiabetic and antiinflammatory effect[J]. Int J Biol Macromol, 2020, 153: 256- 263. doi: 10. 1016/j.ijbiomac.2020.03.009.
[31] SILVA M R O B D, M DA SILVA G, SILVA A L F D, et al. Bioactive compounds of Arthrospira spp. (spirulina) with potential anticancer activities: a systematic review[J].  ACS Chem Biol, 2021, 16 (11): 2057-2067. doi: 10. 1021/acschembio.1c00568.
[32] COUÉ M, TESSE A, FALEWÉE J, et al. Spirulina liquid extract protects against fibrosis related to non-alcoholic steatohepatitis and increases ursodeoxycholic acid [J]. Nutrients, 2019, 11 (1): 194. doi:10.3390/nu11010194.
[33] KASBI-CHADLI F, COUÉ M, AGUESSE A, et al. Spirulina liquid extract prevents metabolic disturbances and improves liver sphingolipids profile in hamster fed a high-fat diet[J]. Eur J Nutr, 2021, 60(8):4483-4494. doi: 10. 1007/s00394-021-02589-x.
[34] OULD AMARA-LEFFAD L, RAMDANE H, NEKHOUL K, et al. Spirulina effect on modulation of toxins provided by food, impact on hepatic and renal functions [J] . . Arch Physiol Biochem, 2019, 125 (2): 184-194. doi: 10. 1080/13813455.2018.1444059.
[35] MA P, HUANG R, JIANG J, et al. Potential use of C-phycocyanin in non-alcoholic fatty liver disease [J].  Biochem Biophys Res Commun, 2020, 526(4):906-912. doi: 10. 1016/j.bbrc.2020.04.001.
[36]ICHIMURA M, KATO S, TSUNEYAMA K, et al. Phycocyanin prevents hypertension and low serum adiponectin level in a rat model of metabolic syndrome[J]. Nutr Res, 2013, 33(5): 397-405. doi: 10. 1016/j.nutres.2013.03.006.
[37] COUÉ M, CROYAL M, HABIB M, et al. Perinatal administration of C-phycocyanin protects against atherosclerosis in apoE-deficient mice by modulating cholesterol and trimethylamine-N-oxide metabolisms[J]. Arterioscler Thromb Vasc Biol, 2021, 41(12): e512-e523. doi: 10. 1161/ATVBAHA.121.316848.
[38]REN Z, XIE Z, CAO D, et al. C-phycocyanin inhibits hepatic gluconeogenesis and increases glycogen synthesis via activating Akt and AMPK in insulin resistant hepatocytes [J]. Food Funct, 2018, 9(5): 2829-2839. doi: 10. 1039/c8fo00257f.
[39]OU Y, REN Z, WANG J, et al. Phycocyanin ameliorates alloxan- induced diabetes mellitus in mice :involved in insulin signaling pathway and GK expression [J]. Chem Biol Interact, 2016, 247: 49- 54. doi: 10. 1016/j.cbi.2016.01.018.
[40] XIA D, LIU B, XIN W, et al. Protective effects of C-phycocyanin on alcohol-induced subacute liver injury in mice [J].  Journal of Applied Phycology, 2015, 28(2):765-772. doi: 10. 1007/s10811- 015-0677-3.
[41] XIE Y, LI W, ZHU L, et al. Effects of phycocyanin in modulating  the intestinal microbiota of mice [J].  Microbiologyopen, 2019, 8 (9): e00825. doi: 10. 1002/mbo3.825.
[42]LIU Q, LI W, QIN S. Therapeutic effect of phycocyanin on acute liver oxidative damage caused by X-ray[J]. Biomed Pharmacother, 2020, 130: 110553. doi: 10. 1016/j.biopha.2020.110553.
[43]SONG Y N, CHEN J, CAI F F, et al. A metabolic mechanism analysis of fuzheng-huayu formula for improving liver cirrhosis with traditional chinese medicine syndromes [J]. Acta Pharmacol Sin, 2018, 39(6): 942-951. doi: 10. 1038/aps.2017.101.
[44]XIAO J, WANG F, WONG N K, et al. Global liver disease burdens and research trends : analysis from a chinese perspective[J]. J Hepatol, 2019, 71(1):212-221. doi: 10. 1016/j.jhep.2019.03.004.
#phycocyanin #cphycocyanin #phycocyaninspirulina
3 notes · View notes
petfurri · 8 months ago
Text
Captopril for Dogs: Benefits, Dosage, Side Effects, and More
Captopril for Dogs
Captopril is an angiotensin-converting enzyme (ACE) inhibitor commonly used in veterinary medicine to manage heart conditions in dogs, particularly congestive heart failure (CHF) and systemic hypertension (high blood pressure). Initially developed for human use, captopril has found its place in treating canine patients with cardiovascular issues, offering numerous benefits but also requiring careful administration and monitoring due to potential side effects.
Understanding Captopril and Its Mechanism of Action
Captopril works by inhibiting the angiotensin-converting enzyme, which is responsible for converting angiotensin I into angiotensin II, a potent vasoconstrictor. Angiotensin II causes blood vessels to narrow, leading to increased blood pressure and making the heart work harder. By blocking this conversion, captopril allows blood vessels to relax and widen, reducing the workload on the heart and lowering blood pressure. This action is particularly beneficial for dogs suffering from CHF, as it helps to improve blood flow and reduce fluid buildup in the lungs and other tissues.
Benefits of Captopril for Dogs
Managing Congestive Heart Failure (CHF): CHF is a common condition in dogs, especially in older or certain breeds like Cavalier King Charles Spaniels. Captopril helps manage CHF by reducing the resistance the heart faces when pumping blood, thus improving cardiac output and reducing symptoms like coughing, difficulty breathing, and lethargy.
Lowering Blood Pressure: For dogs diagnosed with systemic hypertension, captopril can effectively lower blood pressure, preventing damage to organs such as the kidneys, eyes, and brain, which can result from prolonged high blood pressure.
Improving Quality of Life: By easing the burden on the heart and lowering blood pressure, captopril can significantly improve a dog's overall quality of life. Dogs may exhibit increased energy levels, better appetite, and greater overall comfort as a result of treatment.
Potential Renal Protection: In some cases, captopril may offer renal protection by reducing the progression of kidney disease, particularly in dogs with proteinuria (protein in the urine), which is often associated with high blood pressure.
Dosage and Administration
The dosage of captopril for dogs must be carefully determined by a veterinarian, as it varies depending on the dog's weight, the severity of the condition being treated, and the presence of any other health issues. Captopril is usually administered orally, with or without food, typically two to three times a day.
Typical Dosage: The usual starting dose is around 0.5 to 2 mg per kg of body weight, given every 8 to 12 hours. The dosage may be adjusted based on the dog’s response to the medication and any side effects observed.
Monitoring: Regular monitoring is crucial when a dog is on captopril. Blood pressure, kidney function (via blood tests for creatinine and blood urea nitrogen levels), and electrolyte levels should be checked periodically to ensure the medication is working effectively without causing harm.
Potential Side Effects of Captopril
While captopril can be highly beneficial, it also carries the risk of side effects, particularly if not used correctly. Some of the potential side effects include:
Gastrointestinal Issues: Dogs may experience vomiting, diarrhea, or loss of appetite. These symptoms are usually mild but should be reported to the veterinarian if they persist.
Hypotension (Low Blood Pressure): As captopril lowers blood pressure, there is a risk that it may cause blood pressure to drop too low, leading to weakness, dizziness, or fainting. This is more likely to occur in dogs that are dehydrated or have other underlying health conditions.
Kidney Dysfunction: Captopril can affect kidney function, particularly in dogs with pre-existing kidney issues. It’s important to monitor kidney parameters closely during treatment to avoid exacerbating any renal problems.
Hyperkalemia (High Potassium Levels): Captopril can cause an increase in potassium levels, which can lead to dangerous heart rhythms if not managed properly. Regular blood tests are essential to monitor electrolyte levels.
Coughing: A persistent dry cough is a less common side effect but can occur due to the buildup of bradykinin, a substance that captopril can increase in the body.
Allergic Reactions: Though rare, some dogs may have an allergic reaction to captopril, manifesting as itching, rash, or swelling. Immediate veterinary attention is required in such cases.
Precautions and Considerations
Captopril should be used with caution in dogs with pre-existing kidney disease, dehydration, or electrolyte imbalances. It should not be used in dogs that are pregnant, as it can cause harm to the developing fetus. Additionally, it’s important to inform the veterinarian of any other medications the dog is taking, as captopril can interact with other drugs, including diuretics and nonsteroidal anti-inflammatory drugs (NSAIDs), potentially leading to adverse effects.
2 notes · View notes
nursingwriter · 11 days ago
Text
Critical Pathway: Chronic Renal Failure Advanced Pathophysiology Regents Online Degree Program Critical Pathway: Chronic renal failure Chronic renal failure is often occasioned by chronic kidney disease, immune disorder, trauma among other conditions. It does not have any specific symptoms and might include feeling unwell generally and experiencing a reduced appetite. It is diagnosed following screening of individuals who are identified to be at risk of kidney problems, like individuals with diabetes or high blood pressure and others who have blood relative with chronic kidney disease. It always seems complex when trying to come up with the right diagnosis for a patient. M.A. is a 60-year-old man who has a stage V chronic kidney disease mainly as a result of diabetic nephropathy and a 12-year of type 2 diabetes. He has symptomatic peripheral vascular insufficiency, and 3 years ago he had undergone coronary artery bypass 3. Within the ten months that passed, Mr. M.A. had been undergoing hemodialysis 3 days in a week for 3.5 hours via left arm arteriovenous fistula. For the last 3 days he had undergone dialysis following his scheduled dialysis on the day of visit. Three months before Mr. M.A. was admitted, he had developed a non-healing left foot ulcer and a critical lower limb ischemia. Several attempts such as vascular intervention to restore sufficient limb blood flow did not produce a positive result, and after two-month he had to undergo a transmetatarsal amputation. After the surgery the patient found that he was developing surgical wound infection, which called for a repeated debridement as well as intravenous vancomycin administration. According to his wife Mr. M.A. was also showing some signs of continuous confusion and had been having visual hallucinations, claiming to be seeing things that never existed in real life. Such signs began some 2 weeks before he was admitted as an intermittent episode. However, the wife could identify any triggering events or temporal pattern for the episodes. Some 2 days which have passed these signs have been more persistent. Such confusion had never been seen from Mr. M.A. As much he was somehow forgetful in the previous years he was still able to take care of himself and perform simple tasks. As a patient he was receiving medication of atorvastatin, atenolol, aspirin, gabapentin, insulin and the recent medication was vancomycin. For several years the patient had been taking 300mg of gabapentin 4 times in a day and this was effectively controlling his diabetic neuropathic pain. Administering of vancomycin was done during hemodialysis as per the blood levels. His wife made sure that he followed his mediation and dialysis regime strictly. Physical Examination Mr M.A. was somnolent and a febrile but arousable. Some of his critical signs included: Height- 4 feet Weight- 120 lbs Pulse rate of 60 beats/min (regular). Blood pressure of 138/88 mm Hg Respiration rate of 14 breaths/min Temperatures 98.1 (oral) Oxygen saturation while breathing room air of 98% Left metatarsal stump wound was healing Euvolemic without pericardial rubs Waking up periodically Lab results included the following: Abnormal Normal Hemoglobin 11.1 g/dL 13.5-17.5 g/dL White blood cells 5.7 x 109/L 3.5 -- 109/L Platelets 225 x 109/L 150-450 X 109/L Potassium 5.3mEq/L 3.6-4.8mEq/L Sodium 140 mEq/L 135-145 mEq/L Chloride 103 mEq/L 100-108 mEq/L Bicarbonate 20 mEq/L 22-29 mEq/L Glucose 130 mg/dL 70-100 mg/dL Creatinine 5.1 mg/dL 0.8-1.3 mg/dL Blood urea nitrogen 50 mg / dL 8-24 mg/dL When head MRI was done it revealed mild brain atrophy without mass lesion, hemorrhage, or ischemia. Revelation of electroencephalography was that nonepileptogenic, mild bitemporal slowing. Mr. M.A. was put on a full dialysis session, and 2 hours after dialysis as well as prior to dosing, the level of gabapentin were 27.0 ?g/Ml. This is due to the fact that circulating gabapentine is an eliminating efficiency at the time of dialysis. Such a level shows the tissue rebound and reveals that the predialysis level of this patient was clearly elevated. Assessment Causes of the Patient's altered mental status Patients with multiple comorbid conditions are at risk of altered mental status and it can be facilitated by various acute illnesses. Sometimes, it can be the sole symptoms of systemic infection. Consequently, some of the infections like urinary tract infections and pneumonia is suppose to be included within the differential diagnosis and then ruled out. But Mr. M.A. was a febrile, did not have urinary or respiratory symptoms, and was just recently when he was treated with antibiotic. Meaning that it is not likely that infection was the cause of these problems. Stroke is known to be associated with hallucinations and intermittent symptoms of altered mental status, particularly when there are no focal neurologic deficits, implying that it is not likely for stroke to be the cause of these problems. Parkinson-like motor disorder or Parkinson disease is associated with Lewy Body Dementia (LBD). Those patients who are experiencing LBD use to show complex hallucinations and fluctuations in alertness in people. It is known that hallucinations may bring a movement disorder and dementia. As much as LBD may seem to be consistence with the problem of Mr. M.A., the sudden start as well as fast progression would be extremely uncharacterized in LBD, ruling out its possibility. Following Mr. M.A. having history of adherence to regular dialysis in addition to non-presence of uremia's physical signs indicate that hallucinations and decrease alertness are not a result of uremia. Again, during initiation of dialysis he was uremic but failed to demonstrate the same symptoms. It is important to note that in recent weeks, the patient was given multiple agents such as contrast agents for computed tomography and magnetic resonance plus postoperative and preoperative antibiotics. Therefore, the potential and likely cause of the patient's problem could have been medication toxicity, particularly in the setting of renal failure. On the day of his admission, the patient underwent dialysis, and there was an immediate improvement of his hallucinations but came back again during the dialysis sessions. Discussion Mr. M.A. has been known to have Type 2 diabetes which is a chronic condition that always affects the manner in which the body of a person metabolizes glucose (sugar), which is the main source of fuel. It was once known as non-insulin dependent diabetes or an adult-onset. When a person is diagnosed with type 2 diabetes, it means that the body either is failing to produce enough insulin that helps in maintaining a normal glucose level, or the body is resisting the effects of insulin (a hormone that helps in regulating the movement of sugar into the body cell), (Ahern J, Kruger DF., 1989). Though the condition is untreatable, it can be managed by eating well, doing exercises as well as maintaining a healthy weight. Following continuous changes that are taking place within the health care system as well as public policy, there has been a shift in the treatment of renal chronic related acute settings like hospitals, towards outpatient managed care organizations and facilities. The need to achieve a cost-effective treatment is on the rise. Health care professionals specializing in the care of people with renal chronic and other similar illnesses are increasingly being recognized as an important group even in the manner in which they carefully attend to these patients. In the attempt to promote health and prevent occurrence of these related disorders, the health care provider have realized the need for self-management. The patients as well as those who take care of them are trained and educated on how to manage themselves or those who they take care of without necessarily having to visit health facility everyday. Mr. M.A. has also undergone surgery, has wound infection and undergone dialysis. What provided clues for active infection and do away with substantial electrolyte abnormalities and hypoglycemia was an electrolyte panel with measurement concentration of glucose as well as a CBC. Even though there was unlikely of seizure following the history of the patient, useful corroborative information could be based on electroencephalography. MRI of the head can be used to evaluate structural abnormalities like mass lesion and brain atrophy. Elimination of gabapentin takes place from the urine, and accumulates in blood if you are a patient with renal failure. When gabapetin is excessively accumulated it may cause different neurologic toxicities, such as coma and hallucination. Therefore the level of gabapentin should be obtained. It would be of little help to consider arterial blood gas since the patient does not manifest respiratory signs and symptoms of oxygen saturation and labored breathing when the breathing room air was 98%. Generally, gabapentine is usually well absorbed and has not been identified to exhibit batch-to-batch variations in it bioavailability. While in the blood stream, it is not bound by protein, (Luer MS, Hamani C, Dujovny M, et al. (1999). Therefore having co-administered medications that tend to bind serum protein is not supposed to have an effect on the gabapentin circulation level. Since gabapentin is usually not metabolized hepatically, it should not be affected by variations of the hepatic cytochrome system activities and any of the effects it has is not inhibited or induced by co-administered hepatic medications, (Blum RA, Comstock TJ, Sica DA, et al., 1994). As a result, it is unlikely that pharmacokinetic or molecular drug-drug interactions accounts for accumulation of gabapentin. Mr. M.A. has been following his prescribed medication and any form of acute overdosing has not been revealed by either him or his wife. Gabapentin is excreted renaly. Reducing the capacity of renal excretion may in turn rise up the blood level of gabapentin, eliciting neurologic symptoms, as was indicated before. The patient had previously started undergoing dialysis and the expectation to achieve a substantial residual renal clearance, (Spafford JD, Zamponi GW., 2003). But, since there was a repeated exposure of the patient to intravenous contrast agent for limb ischemia evaluation, might have eradicated his residual clearance, resulting to accumulation of gabapentin. In the past several months, Mr. M.A. has been adhering to the dialysis regime, and the delivered dialysis has been adequate. Therefore, the issue of inadequate dialysis is not likely to be the man inciting factor. When the patient was questioned further, he admitted that he had a progressive decline in urine output and almost anuric at the time of admission. Due to the loss of residual kidney function might have been the caused by the increasing gabapentin accumulation. Risk factors A consideration can be on ?-Blocker since they have been known to slow down the release of certain adrenergic neurotransmitters. Yet, it is generally thought that analgesic effect of gabapentin lie in the blockage of presynaptic release of neurotransmitters, as well as serontonin, norepinephrine, and acetylcholine. It is not known that ?-blockers alter gabapentin's effect. Most of the patient for many years has been taking gabapentin and atenolol concurrently without apparently realizing any toxic. Even with the actively transportation of gabapentin to brain tissues, there have not been signs of atherosclerotic vascular changes to alter the pattern of its distribution or diminishing its entry to brain tissue, (Wong MO, Eldon MA, Keane WF, et al.(1995). It has remained effective for controlling pain in patients who have severe atherosclerotic vascular disease. The major cause of kidney failure of Mr. M.A was diabetic nephropathy. On the other hand, diabetic nephropathy has not been known to bring forth a prediction for gabapentin-induced neurotoxicity, as well as hallucinations, over the rest of kidney failure causes. Gabapentin inhibiting presynaptic Ca 2+ influx tend to be the main putative mechanism leading to the desired effects of analgesic, (Catterall WA., 2000). This mechanism may account for the fundamental neurotoxicity causes. Severe, mild, or dementia tends to be associated with an augmented incidents of gabapentin-induced changes within the mental status, (Dogukan A, Aygen B, 2006). For patients who happens to have mild dementia, the evidence shows that gabapentin worsen dramatically the neuropsychiatric disturbances, resulting to a complex dominated psychoagitation through persistent hallucinations and ideas of reference. Since Mr. M.A. is having loss of memory, indicating some signs of dementia, a condition might have been the one that landed him to neuropsychiatric symptoms that was triggered by gabapentin toxicity. Interventions An individual with normal kidney clearance will have a kidney that excretes gabapentin with a half life of 5 to 7 hours. For patients who are experiencing a reduced kidney function, the increase of their half-life is up to 132 hours without dialysis. Dosing range for gabapentin patients experiencing chronic kidney dysfunction from stage III to V is always 100 to 1400 mg/d. But, dosing should be further raised for individual patients based on the level of kidney failure as well as the estimated drug half-life.Gabapentin's tissue content tend to be linearly proportional to the blood level, and there is effective removal of circulating gabapentin by hemodialysis. When the dosage is reduced while dosage frequently remains may lead to an initial sub-therapeutic drug level once the dialysis and a supratherapeutic level has been carried out before the next session of dialysis. Consequently, it is not appropriate to cut just down the dosage such as by 100 mg 3 times daily. The dosage is supposed to be reduced by frequency of 300 mg once a dialysis has been carried out and this maintains sufficient blood level, and this is what Mr. M.A. needs. Since he was experiencing neuropathic pain, gabapentin should be used in controlling the pain. Central nervous system depression secondary to benzodiazepines will be reversed by Flumazenil. It has been known for treatment of gabapentin toxicity, (Raudino F, Mascalzi MG, Zagami A., 2004). Mr. M.A. received a measure by withholding gabapentin for a day and reinintitiated at 300 mg after 3 times per week. As a result the level of his predialysis gabapentin went down to 16.6 ?g/mL, thereby restoring his mental baseline. Discussion The case of Mr. M.A. is an example of complexity experienced when caring for patients with chronic kidney disease as well as multiple comorbid conditions. It shows how a devastating toxicity may take place with what one may consider to be a well-tolerated medication; which can even be at the reference dosing range. Chronic kidney failure is well-known global epidemic, and among the main causes is diabetes, (Coresh J, Selvin E, Stevens LA, et al., 2007). Those who are suffering form diabetes and nephropathy tend to display a common concurrent diabetic neuropathy. Palliating of neuropathic pain has been frequently done by gabapentin. In United States gabapentin became released in 1993 to act as an anticonvulsant agent. Several clinical and preclinical trials across different states, has identified gabapentin to be a well tolerated and effective anticonvulsant agent and also anxiolytic as well as analgesic agent, (Rossi P, Serrao M, Pozzessere G., 2002). Recently, its use has increasingly been off-label for expanded indications, such as diabetic neuropathy, hot flashes, uremic pruritus, and phantom limb pain. An analogue of ?-aminobutyric acid (C9H17NO2) and a water-soluble 1-(aminomethyl)-cyclohexaneacetic acid crosses readily the blood brain barrier and transported actively into the brain tissues through system L. It is shown that the concentration of gabapentin in brain tisues is the same as or higher than the one in blood, (Brawek B, Loffler M, 2008). Even though the experimental data shows that gabapentin mediates analgesia through presynaptic VSCC inhibition, those who investigate have again discovered the existence of lower well-defined, "2"-1 -- mediated regulatory pathways, that is independed to the functions of VSCC. Therefore, there has not been a fully elucidated complete effect of spectrum of gabapentin-mediated pharmacologic and toxicologic. In addition, under physiologic conditions, gabapentin usually shows minimal effects, however, it clearly alters synaptic neurotransmitter's profile at the time of neuronal hyperexcitability. Hence, end results in patients who experience functional and structural alterations of the brain. Gabapentin that is absorbed well from the gastrointestinal tract, tend to have a consistent of 50% to 60% bioavailability, and is not altered in those with kidney dysfunction. While circulating, it has not been bound by metabolized or protein. Even though a target degree of blood has not been defined, 8 to 20 ?g/mL has found to have a correlation with clinical efficiency, (Wen CP, Cheng TY, Tsai MK, et al., 2008). Elimination of gabapentin in urine is at arate which is proportional to clearance of creatinine. Therefore, with preserved gastrointestinal absorption and progressive kidney failure, diminishing kidney elimination can create a considerable gabapentin toxicity risk. A clue to the diagnosis Mr. M.A. may have been manifested by the transient improvement in mental status immediately after hemodialysis. This is due to the fact that gabapentin can be dialyzed readily, for example a post dialysis level of 26.4 ?g/mL could predict a highly increased predialysis level in at least the mid 40s. Some other clue to potential gabapentin toxicity may have been the reduction of urine output that resulted to the onset of neurologic symptoms, (Bassilios N, Launay-Vacher V, 2001). Many of the patients for along time have been given similar dosage of gabapentin without manifestations of neurologic. Such a possibility was evident after there was a decrease of predialysis gabapentin to the required level after the dose was reduced. At the same time the patient regained his mental alertness and there were no more hallucinations. Conclusion There are many points to be deduced from this case. Residual kidney function is essential for patients who are receiving long-term dialysis and when a patient experience loss of residual function, it may result to a very serious clinical outcome, moreover it is supposed to be considered in formulating a diagnosis; A well tolerated medication with an excellent pharmacokinetic profile is capable of causing an overwhelming and potentially life-threatening toxicities; Those patients who are experiencing initial dementia are at risk of having mental status alteration following system disorder, as well as drug toxicity; Even within the general reference dosing range, still medication toxicity may occur in patients with kidney failure. The patient patients use to receive an inappropriately high dosage of gabapentin even prior to the loss of residual kidney clearance. The patient's residual kidney clearance seems to have barred him from developing overt toxicity. Therefore, it is of importance for tailoring of drug dosing to these patients and be followed by a continuous monitoring. Medical care for patients who are elderly and experience kidney dysfunction as well as multiple comorbid conditions has increasingly become complex and challenging. Undertaking delicate changes within the baseline of functional organ is capable of having a dramatic effect to the patient's response to treatment. However, by taking these complexities into consideration will prevent excessive investigative work-ups as well as improve the quality of our healthcare services. Read the full article
0 notes
dietitiananuradha · 12 days ago
Text
How to Balance Protein Intake for Kidney Health
The kidneys are two bean-shaped organs about the size of a fist. They are situated right below the rib cage on each side of your spine. Every minute, healthy kidneys filter almost half a cup of blood, eliminating waste and excess water to create urine. Urine passes from the kidneys to the bladder via two ureters, one on each side. It is stored in the bladder. Your kidneys, ureters, and bladder are all part of your urinary tract.
Tumblr media
The kidneys are powerful chemical factories that perform the following functions:
The kidneys are vital organs that function as powerful chemical factories in the body. They perform several essential tasks, including:
Filtering Waste and Toxins: . Remove waste products and excess fluids from the blood through urine. .Eliminate toxins and byproducts of metabolism, such as urea and creatinine.
Regulating Blood Pressure: . Control blood pressure by balancing fluid levels and releasing hormones like renin.
Balancing Electrolytes and pH: . Maintain proper levels of sodium, potassium, calcium, and phosphorus. . Help regulate the body’s acid-base (pH) balance.
Producing Hormones and Enzymes: .Secretes erythropoietin (EPO) to stimulate red blood cell production in the bone marrow. .Activate vitamin D to maintain strong bones and calcium balance.
Controlling Fluid Balance: . Regulate the amount of water retained or excreted, preventing dehydration or fluid overload.
Removing Drugs and Toxins: . Process and eliminate medications, chemicals, and toxins from the body.
Supporting Healthy Metabolism: .Contributes to glucose metabolism and may play a role in glucose production during fasting.
Maintaining kidney health is crucial for overall well-being, as these organs work tirelessly to stabilize the body’s internal environment.
How to Intake Protein Wisely
Know Your Protein Requirement . The ideal protein intake depends on individual health conditions. . For people with kidney issues, dietitians often recommend 0.8 grams of protein per kilogram of body weight per day (lower than the usual 1.0 g/kg for healthy individuals).
Balance Protein with Other Nutrients . Combine proteins with fiber-rich vegetables and healthy fats for balanced meals. . Avoid excessive salt and processed foods, which can further burden the kidneys.
Choose Plant-Based Proteins More Often . Replace some animal proteins with legumes, nuts, and whole grains to reduce the nitrogenous waste that kidneys need to filter. . Limit phosphorus-rich plant proteins like soy in moderation, as high phosphorus can affect kidney function.
Cook Smartly . Grilling, steaming, or baking proteins instead of frying keeps them healthier. . Reduce salt and processed sauces, which can increase kidney strain.
Monitor Portion Sizes . Instead of consuming large amounts in one meal, spread protein intake evenly throughout the day to ease the kidney workload.
Stay Hydrated . Drinking enough water supports kidney function and helps flush out excess protein waste. Consult for determining water intake as it might be restricted according to the grade of kidney disease.
Final Thoughts
Balancing protein intake is essential for protecting kidney health. While protein is necessary for bodily functions, excess consumption, especially from animal sources, can overwork the kidneys. By choosing high-quality, moderate-protein sources, incorporating plant-based options, and monitoring portion sizes, you can support your kidney function while maintaining overall well-being.
For personalized guidance, always consult a doctor or nutritionist to determine the right protein intake based on your specific kidney health needs. Consult Dietitian Anuradha to balance your life, be healthy and happy.
0 notes
bharathomoeopathy · 22 days ago
Text
Natural Cure for Chronic Kidney Disease - A Homeopathic Approach by Bharathomeopathy
Chronic Kidney Disease (CKD) is a severe health condition that affects millions of people worldwide. It gradually reduces kidney function, leading to dangerous complications if left untreated. Conventional treatments often include medications and dialysis, but many patients seek a natural and holistic cure for chronic kidney disease to improve their quality of life without invasive procedures. At Bharathomeopathy, we specialize in providing homeopathic solutions that help manage and reverse kidney problems effectively and naturally.
Tumblr media
Understanding Chronic Kidney Disease (CKD)
The kidneys are vital organs responsible for filtering waste and excess fluids from the blood. When kidney function declines, harmful toxins accumulate, leading to serious health complications. CKD progresses in five stages, with the final stage requiring dialysis or a kidney transplant. However, with the right kidney problem medication, early-stage CKD can be managed, and further deterioration can be prevented.
Symptoms of Chronic Kidney Disease
Patients with CKD often experience symptoms such as:
Fatigue and weakness
Swelling in the legs, ankles, and feet
Frequent urination, especially at night
Blood in the urine or foamy urine
High blood pressure
Loss of appetite and nausea
Shortness of breath
Recognizing these symptoms early and opting for a natural chronic kidney disease treatment can prevent kidney damage from worsening.
Homeopathy - A Holistic Approach to CKD
At Bharathomeopathy, we believe that the body has an innate ability to heal itself. Our homeopathic approach focuses on stimulating this self-healing mechanism. Unlike conventional medicine, which often suppresses symptoms, homeopathy targets the root cause of CKD, offering a sustainable and effective kidney failure treatment without dialysis.
Benefits of Homeopathic Treatment for CKD
Improves Kidney Function Naturally: Homeopathic medicines help rejuvenate kidney cells and enhance their functionality.
Reduces Symptoms Without Side Effects: Unlike allopathic medicines, homeopathy does not cause adverse effects on other organs.
Prevents Further Kidney Damage: By balancing the body's immune response, homeopathy prevents CKD from progressing to advanced stages.
Enhances Overall Well-Being: Our treatment not only focuses on kidney health but also improves digestion, energy levels, and immunity.
Effective Homeopathic Kidney Problem Medication
Homeopathy offers a range of effective remedies that help restore kidney function. Some commonly used homeopathic medicines for CKD include:
Apis Mellifica: Beneficial for reducing swelling and water retention.
Arsenicum Album: Helps in managing fatigue, nausea, and protein loss in urine.
Berberis Vulgaris: Supports kidney filtration and prevents stone formation.
Lycopodium: Effective for managing high creatinine levels and urinary issues.
Serum Anguillae: Aids in reducing urea and creatinine levels naturally.
Each remedy is prescribed based on the patient’s individual symptoms and medical history, ensuring a personalized chronic kidney disease treatment.
Lifestyle and Dietary Recommendations for CKD Patients
Along with homeopathic treatment, a balanced lifestyle and healthy diet are essential for managing CKD effectively. Here are some expert recommendations from Bharathomeopathy:
Dietary Tips:
Reduce sodium intake to prevent high blood pressure and fluid retention.
Limit protein consumption to reduce kidney strain.
Increase water intake to flush out toxins naturally.
Avoid processed foods and artificial sweeteners.
Include kidney-friendly foods like cabbage, bell peppers, apples, and berries.
Lifestyle Modifications:
Maintain a healthy weight through regular exercise.
Manage blood sugar levels to prevent diabetic nephropathy.
Control blood pressure with meditation and stress management techniques.
Avoid smoking and excessive alcohol consumption.
Why Choose Bharathomeopathy for CKD Treatment?
1. Personalized Treatment Plans
Each patient receives a customized treatment plan based on their symptoms, medical history, and lifestyle habits.
2. Natural and Side-Effect-Free Medicine
Our homeopathic remedies are derived from natural sources and do not cause harmful side effects.
3. Expert Guidance from Experienced Homeopaths
Our team of skilled homeopathic practitioners specializes in treating kidney disorders effectively.
4. Comprehensive Support
We provide holistic support, including diet plans, lifestyle guidance, and continuous monitoring to ensure the best results.
Conclusion
Chronic Kidney Disease does not have to lead to dialysis or a kidney transplant. With the right kidney failure treatment without dialysis, it is possible to manage and even reverse kidney damage naturally. At Bharathomeopathy, we are committed to providing safe, effective, and personalized homeopathic solutions to restore kidney health and improve overall well-being. If you or your loved ones are looking for a reliable cure for chronic kidney disease, get in touch with us today and take the first step towards a healthier life!
0 notes
aayushhospitals · 26 days ago
Text
Understanding Kidney Failure: Causes, Symptoms, and Treatment Options
Kidney failure, also known as end-stage renal disease (ESRD), is a serious condition where the kidneys lose their ability to function properly. The kidneys play a crucial role in filtering waste, balancing electrolytes, and maintaining overall body health. When they fail, it can lead to life-threatening complications. In this blog, we will discuss the causes, symptoms, and treatment options for kidney failure, along with the importance of seeking medical care from the Best Nephrology Hospital in Bhuj. 
What is Kidney Failure? 
Kidney failure occurs when the kidneys lose their ability to remove waste and excess fluids from the blood. This leads to a buildup of toxins in the body, causing severe health problems. Kidney failure can be acute (sudden) or chronic (gradual), and both types require immediate medical attention. 
If you are experiencing kidney-related health concerns, it is essential to visit a Top Kidney Hospital in Bhuj to get a proper diagnosis and treatment plan. 
Causes of Kidney Failure 
Several factors can contribute to kidney failure, including: 
1. Diabetes 
High blood sugar levels damage the kidney’s filtering units over time, leading to chronic kidney disease (CKD) and eventually kidney failure. 
2. High Blood Pressure (Hypertension) 
Increased blood pressure damages kidney blood vessels, making it difficult for them to function properly. Long-term hypertension is one of the leading causes of kidney failure. 
3. Glomerulonephritis 
This is an inflammation of the kidney’s filtering units, which can lead to chronic kidney damage. 
4. Polycystic Kidney Disease (PKD) 
A genetic disorder that causes cysts to form in the kidneys, reducing their ability to function. 
5. Urinary Tract Blockage 
Kidney stones, tumors, or an enlarged prostate can block urine flow, leading to kidney damage. 
6. Infections and Autoimmune Diseases 
Certain infections and autoimmune disorders, such as lupus, can damage the kidneys and lead to failure. 
Seeking early intervention at the Best Nephrology Treatment in Bhuj can prevent further complications and improve kidney health. 
Symptoms of Kidney Failure 
Kidney failure often develops gradually, and symptoms may not appear until significant damage has occurred. Common symptoms include: 
Persistent fatigue and weakness 
Swelling in the legs, ankles, and feet 
Decreased urine output or changes in urination frequency 
Shortness of breath due to fluid buildup in the lungs 
High blood pressure that is difficult to control 
Nausea, vomiting, and loss of appetite 
Confusion, memory problems, or difficulty concentrating 
Muscle cramps and twitching 
Skin itching and dryness 
If you experience any of these symptoms, consult the Best Nephrologist in Bhuj for an accurate diagnosis and treatment plan. 
Diagnosis of Kidney Failure 
To diagnose kidney failure, doctors perform several tests, including: 
1. Blood Tests 
These tests measure creatinine and blood urea nitrogen (BUN) levels, which indicate kidney function. 
2. Urine Tests 
A urine analysis helps detect abnormalities such as protein leakage or blood in the urine. 
3. Imaging Tests 
Ultrasounds, CT scans, or MRIs help identify structural abnormalities in the kidneys. 
4. Kidney Biopsy 
A small tissue sample is taken from the kidney to determine the extent of damage. 
Getting diagnosed at a Kidney Hospital in Bhuj ensures access to advanced medical technology and specialized care. 
Treatment Options for Kidney Failure: 
The treatment approach for kidney failure depends on its cause and severity. Common treatment options include: 
1. Lifestyle and Dietary Changes 
Patients with mild kidney disease can manage their condition through: 
A low-sodium diet to control blood pressure 
Reducing protein intake to lower the workload on the kidneys 
Staying hydrated and avoiding harmful substances like alcohol and tobacco 
2. Medications 
Doctors may prescribe medications to: 
Control blood pressure 
Reduce cholesterol levels 
Manage diabetes 
Treat anemia 
3. Dialysis 
Dialysis is a procedure that removes waste, excess fluids, and toxins from the blood when the kidneys can no longer function adequately. There are two types: 
Hemodialysis: Blood is filtered using a dialysis machine. 
Peritoneal Dialysis: A cleansing fluid is used inside the abdomen to remove waste. 
Dialysis is a life-sustaining treatment available at the Best Nephrology Hospital in Bhuj. 
4. Kidney Transplant 
A kidney transplant is the best option for long-term survival in patients with end-stage renal disease. In this procedure, a healthy kidney from a donor is implanted into the patient. The success rate for kidney transplants is high, especially when performed at a Top Kidney Hospital in Bhuj. 
Preventing Kidney Failure 
While some causes of kidney failure are unavoidable, adopting healthy habits can reduce the risk of kidney disease: 
Control Diabetes and Hypertension: Regular monitoring and medication management can prevent kidney damage. 
Stay Hydrated: Drinking enough water helps kidneys flush out toxins. 
Eat a Balanced Diet: Reduce sodium, processed foods, and excessive protein intake. 
Exercise Regularly: Physical activity helps maintain a healthy weight and blood pressure. 
Avoid Overuse of Painkillers: Nonsteroidal anti-inflammatory drugs (NSAIDs) can damage the kidneys over time. 
Regular Health Check-ups: Early detection of kidney issues can prevent disease progression. 
For expert guidance on kidney health, visit Aayush Hospitals for the Best Nephrology Treatment in Bhuj. 
Why Choose Aayush Hospitals for Kidney Care? 
Aayush Hospitals is renowned for providing top-tier nephrology care. Here’s why we are the Best Kidney Hospital : 
Experienced Nephrologists: Our specialists are highly trained in diagnosing and treating kidney diseases. 
Advanced Dialysis Facilities: We offer state-of-the-art dialysis units with expert monitoring. 
Comprehensive Kidney Transplant Program: We provide top-notch transplant services with high success rates. 
Personalized Treatment Plans: Our approach focuses on customized care for each patient. 
24/7 Emergency Care: Our team is available around the clock for urgent kidney-related emergencies. 
Conclusion 
Kidney failure is a serious but manageable condition with the right treatment and lifestyle choices. Early detection, timely medical intervention, and expert care from the Best Nephrologist in Bhuj can significantly improve the quality of life for kidney disease patients. 
If you or a loved one are experiencing kidney-related symptoms, don’t delay seeking medical help. Aayush Hospitals, the Top Kidney Hospital in Bhuj, is here to provide comprehensive and advanced nephrology care. 
For consultations and appointments, visit Aayush Hospitals today and take the first step toward better kidney health! 
0 notes
asto-labs · 2 months ago
Text
The Complete Guide to Kidney Profile Checkup
Maintaining kidney health is essential for overall well-being, as these vital organs play a crucial role in filtering waste, balancing fluids, and regulating blood pressure. A kidney checkup in Chennai can help detect early signs of kidney-related issues, allowing for timely intervention and treatment.
What Is a Kidney Profile Checkup?
A kidney health checkup in Chennai includes tests designed to assess kidney function. These tests typically measure creatinine levels, blood urea nitrogen (BUN), glomerular filtration rate (GFR), and electrolyte balance to ensure optimal kidney performance.
Who Should Get a Kidney Checkup?
You should consider a kidney checkup package in Chennai if you:
Have diabetes or high blood pressure
Experience symptoms like swelling, fatigue, or frequent urination
Have a family history of kidney disease
Have had kidney stones in the past
Kidney Stone Checkup: Why It’s Important
A kidney stone checkup in Chennai is essential for individuals prone to kidney stones. This test helps detect stones' presence, size, and impact on kidney function. Early detection can prevent complications and reduce the risk of severe pain or kidney damage.
Convenience of a Kidney Checkup at Home
For those who prefer hassle-free health monitoring, a kidney checkup at home in Chennai is a great option. With home-based diagnostic services, you can get tested from the comfort of your home without visiting a clinic or hospital.
Conclusion
Regular kidney screenings are crucial for detecting potential kidney issues early and maintaining overall health. Whether you need a routine kidney profile checkup or a specialized test for kidney stones, Asto Labs offers accurate and reliable diagnostic services.
Book your kidney checkup with Asto Labs today and take the first step toward better kidney health!
0 notes
mangalprabhuhospital · 2 months ago
Text
How To Improve Kidney Function to Avoid Dialysis?
Dialysis is a life-saving treatment for patients who are at an advanced stage of kidney disease. While it may be necessary for those who’ve sustained severe kidney damage, there are ways you can avoid going through dialysis. We’ve compiled a list of the best kidney practices recommended by every nephrologist in Navi Mumbai for good kidney health. These can help improve kidney function, making it more efficient at filtering the waste and excess fluid from your bloodstream. Here’s what can help.
Diet and Nutrition
Your diet plays an important role in keeping your kidneys healthy. You should follow a balanced diet with low sodium, moderate amounts of lean proteins, low-potassium and low-phosphorus foods. Try to include more vegetables, fruits, and low-fat products in your diet to protect your kidneys. You can also consult a registered dietician to create a customized, kidney-friendly diet plan for you.
Hydration
Drink plenty of water to flush out toxins from your body. Hydration dissolves minerals and waste products in your bloodstream, including creatinine and urea. Moreover, the risk of kidney stones increases drastically when you are dehydrated. This leads to highly concentrated urine, which can form mineral deposits that turn into kidney stones. That said, you must not drink too much water, as it can cause water intoxication. Ideally, 6-8 glasses of water are sufficient, but always consult your doctor if you have advanced-stage kidney disease.
Lifestyle Changes
1) Exercise:
Incorporating exercise into your routine can significantly impact your lifestyle and reduce your risk of developing chronic diseases. You don’t have to join a gym or practice high-intensity workouts. Just taking a walk every day, doing household chores, and trying aerobic exercises will do.
2) Avoid Stress:
Managing stress is another vital part of reducing your risk of developing chronic kidney disease. Stress is linked to heightened blood pressure, which can narrow the arteries in the kidneys, affecting their ability to filter out waste effectively. Chronic blood pressure can cause kidney disease. Practice meditation, yoga, and other exercises to manage stress. Consult a professional counselor to discuss the best stress management techniques.
3) Regulate Your Blood Sugar Level:
People with diabetes are also more likely to develop kidney diseases compared to those with regulated sugar levels. Like blood pressure, high blood sugar levels can damage the blood vessels in your kidneys, impairing their function. Monitor your blood sugar regularly and take your prescribed medication, including insulin shots, if prescribed.
Monitoring and Medical Check-ups
Schedule regular health checkups if you have a family history of kidney diseases, high blood sugar, high blood pressure, and other conditions that make you more prone to developing kidney issues. Blood and urine tests can help identify unhealthy kidneys early on. Remember, the sooner it’s diagnosed, the better the chances you won’t need to visit a dialysis center in Navi Mumbai. Seek immediate medical care if you experience reduced urine output, fatigue, nausea, loss of appetite, and shortness of breath. These are some warning signs of severe kidney disease.
0 notes
pathcares · 3 months ago
Text
Full Body Checkup in Noida – Your Guide to Better Health
Tumblr media
In today’s fast-paced life, regular health checkups are essential to detect potential health issues before they become severe. A full body checkup in Noida can help you stay ahead of diseases, ensuring timely diagnosis and treatment. If you are looking for a comprehensive and affordable full body checkup in Noida at home, this guide will help you understand its importance, components, and how to choose the best pathology lab.
Why is a Full Body Checkup Important?
A Full Body Checkup helps in:
Early Detection of Diseases – Identifying health risks before they escalate.
Monitoring Health Status – Keeping track of vital parameters such as blood sugar, cholesterol, and liver function.
Preventive Healthcare – Reducing the chances of chronic conditions like diabetes, heart disease, and kidney disorders.
Peace of Mind – Ensuring overall well-being by assessing multiple organ functions.
What Does a Full Body Checkup Include?
A full body checkup in Noida generally consists of the following tests:
Complete Blood Count (CBC) – Assesses overall health and detects infections or anemia.
Lipid Profile – Measures cholesterol and triglycerides to evaluate heart health.
Liver Function Test (LFT) – Checks liver enzymes and bilirubin levels.
Kidney Function Test (KFT) – Evaluates kidney health by analyzing creatinine and urea levels.
Blood Sugar Test – Helps in diabetes detection and management.
Thyroid Function Test – Ensures proper thyroid gland functioning.
Urine Routine Examination – Detects urinary tract infections and kidney issues.
Electrolyte Panel – Balances body fluids and ensures proper nerve and muscle function.
Vitamin Deficiency Test – Checks levels of Vitamin D, B12, and other essential nutrients.
ECG or Chest X-Ray – For assessing heart and lung health.
Best Pathology Labs for Full Body Checkup in Noida
Finding a reliable pathology lab in Noida is crucial for accurate reports and expert consultation. Here are some factors to consider:
Accreditation – Ensure the lab is NABL-certified for precise testing.
Experience & Reputation – Choose a well-established lab with positive reviews.
Home Sample Collection – Opt for a lab offering full body checkup in Noida at home for convenience.
Turnaround Time – Check for labs providing fast and reliable reports.
Affordable Packages – Compare pricing and discounts for budget-friendly checkups.
How to Book a Full Body Checkup in Noida?
Booking a full body checkup in Noida at home is now easier than ever. Many pathology labs offer online appointment scheduling and home sample collection. Follow these simple steps:
Choose a trusted pathology lab.
Select the Full Body Checkup package that suits your needs.
Book an appointment online or via phone.
Opt for home sample collection or visit the nearest lab.
Get your reports online and consult a doctor for analysis.
Conclusion
Regular health checkups can save lives by detecting diseases at an early stage. If you’re looking for a full body checkup in Noida at home, ensure you choose a reputed pathology lab with advanced testing facilities. Prioritize your health today and book a Full Body Checkup to stay ahead of potential health risks.
For hassle-free full body checkup in Noida at home, contact Dr. Path Cares for affordable and accurate health checkups
0 notes
cleverhottubmiracle · 3 months ago
Photo
Tumblr media
Ideally, your urine should be pale yellow and clear. But if you’ve ever noticed it appears milky or hazy, you may be wondering, “Why is my pee cloudy?” While cloudy pee can be alarming, there’s good news to report: “Cloudy urine is often linked to a few different factors, and it’s not always something to worry about, “ assures Raj Dasgupta, MD, Chief Medical Advisor for Garage Gym Reviews. “Most of the time, once the cause is identified, clearing up cloudy urine can be fairly simple.” Here, we break down what causes cloudy pee, along with the best ways to treat it. Why is my pee cloudy? 5 causes and cures Some of the most common culprits behind cloudy urine include: For a UTI, sip cranberry juice “Urinary tract infections (UTIs) are one of the most common causes of cloudy urine,” says Dr. Dasgupta. “They bring in white blood cells, bacteria and mucus, which can make the urine look cloudy.”  Cloudy urine from a UTI usually comes with other symptoms like a burning sensation when you pee, a constant need to go (even if it’s just a little) and a lower abdominal ache, he adds. “You might also notice a strong, unpleasant smell or even blood in the urine if the infection is more advanced.” Natural remedies like cranberry juice, cranberry supplements or d-mannose can be helpful for easing the discomfort associated with mild UTIs. (See our round-up of the best doctor-backed home remedies for a UTI here.) But Dr. Daguspta cautions they’re not effective treatments for more advanced infections.  Your best bet: Heading to your doctor or a urology specialist for urine tests that can diagnose a UTI and guide antibiotic treatment. “Delaying treatment could make the infection worse or lead to complications, like a kidney infection,” Dr. Dasgupta cautions. “It’s better to act quickly if the symptoms don’t ease up.” For dehydration, drink more water When you’re dehydrated, your urine becomes more concentrated. “This concentration increases the levels of waste products like urea and creatinine, which can cause the urine to appear cloudy,” Dr. Dasgupta explains. Along with cloudy pee, dehydration may cause symptoms like dark yellow or amber-colored urine, a dry mouth, fatigue, dizziness and infrequent urination. Symptoms such as dizziness and confusion can signal severe dehydration that calls for immediate medical attention and IV fluid replacement, adds Aleece Fosnight, PA-C, medical advisor to Aeroflow Urology and board-certified physician assistant .  But Dr. Dasgupta notes that drinking more water can help correct cloudiness caused by milder cases. “Aiming for at least eight cups (about two liters) of water a day is a good rule of thumb, though individual needs may vary,” he says. “The key is to stay well-hydrated throughout the day, which helps keep urine clear and reduces cloudiness.” For a vaginal infection, try a prescription antibiotic or antifungal  “A bacterial infection known as bacterial vaginosis (BV) and yeast infections are among the most common causes of vaginal infections that could lead to cloudy urine,” notes Dr. Dasgupta. “Both conditions are fairly common and can cause noticeable changes in vaginal discharge.” The discharge then mixes with urine to produce cloudiness.  Other clues that a vaginal infection is your cloudiness culprit: “For BV, you might notice a thin, grayish discharge with a fishy smell, along with mild itching or irritation,” Dr. Dasgupta explains. “Yeast infections, on the other hand, usually come with thick, white discharge (like cottage cheese), intense itching and redness.”  If you experience cloudy pee along with the symptoms above, visit your doctor. “While these infections aren’t usually serious, getting the right treatment can help you feel better faster and avoid complications,” Dr. Dasgupta assures. “For BV, antibiotics are typically prescribed, and yeast infections are treated with antifungal medications, either as a cream, vaginal suppository or pill. Most infections clear up within a few days to a week once treatment begins.” For kidney stones, up your fluid intake Kidney stones trigger cloudy pee through two major mechanisms. “One is the kidney stone itself may cause a urinary tract infection that makes urine cloudy,” Fosnight explains. “Two, the kidney stone typically develops from minerals and crystals, which causes cloudiness of the urine secondary to the increased particle concentration.” Cloudiness due to kidney stones can also be accompanied by changes in urine color, especially redness due to hematuria or blood in urine, adds Fosnight. Other symptoms she cites: Flank pain, nausea, vomiting, fever, chills, urinary frequency and/or urgency, dysuria (pain or burning with urination), malodorous urine and decreased urine output. If you experience such symptoms, Fosnight recommends seeing a medical professional who can conduct a CT scan that evaluates the abdomen and pelvis. If kidney stones are detected, treatment differs depending on their size.  “If the stone is 5 mm or less, individuals are typically able to pass them on their own with increased fluids and alpha blocker medications (like Flomax) to help dilate the ureter and ease the passage,” she says. “For stones 5 mm or larger or smaller stones that are not passing on their own, surgical intervention with ureteroscopy (a scope that goes through the ureter) and/or lithotripsy may be required.” For high blood sugar, visit your doctor Normally, your kidneys filter and reabsorb glucose back into the bloodstream. But when blood sugar levels get too high, the kidneys can’t keep up and the extra glucose ends up in your urine. This is a condition called glucosuria that can make pee cloudy, Dr. Dasgupta explains. “Along with cloudy urine, glucosuria can cause a sweet or fruity smell in your pee,” he says. “You might also notice symptoms like excessive thirst, frequent urination or feeling unusually tired—common signs of elevated blood sugar. Infections like UTIs are also more likely in this scenario.” Your best course of action If you think your cloudy pee is related to high blood sugar: Head to your doctor as soon as possible. “Doctors diagnose glucosuria using a simple urine test, often alongside blood tests to confirm high glucose levels and check overall health,” Dr. Dasgupta notes. “Treatment focuses on managing blood sugar, which might include lifestyle changes, medications or insulin, depending on your condition.” This content is not a substitute for professional medical advice or diagnosis. Always consult your physician before pursuing any treatment plan.   Source link
0 notes
norajworld · 3 months ago
Photo
Tumblr media
Ideally, your urine should be pale yellow and clear. But if you’ve ever noticed it appears milky or hazy, you may be wondering, “Why is my pee cloudy?” While cloudy pee can be alarming, there’s good news to report: “Cloudy urine is often linked to a few different factors, and it’s not always something to worry about, “ assures Raj Dasgupta, MD, Chief Medical Advisor for Garage Gym Reviews. “Most of the time, once the cause is identified, clearing up cloudy urine can be fairly simple.” Here, we break down what causes cloudy pee, along with the best ways to treat it. Why is my pee cloudy? 5 causes and cures Some of the most common culprits behind cloudy urine include: For a UTI, sip cranberry juice “Urinary tract infections (UTIs) are one of the most common causes of cloudy urine,” says Dr. Dasgupta. “They bring in white blood cells, bacteria and mucus, which can make the urine look cloudy.”  Cloudy urine from a UTI usually comes with other symptoms like a burning sensation when you pee, a constant need to go (even if it’s just a little) and a lower abdominal ache, he adds. “You might also notice a strong, unpleasant smell or even blood in the urine if the infection is more advanced.” Natural remedies like cranberry juice, cranberry supplements or d-mannose can be helpful for easing the discomfort associated with mild UTIs. (See our round-up of the best doctor-backed home remedies for a UTI here.) But Dr. Daguspta cautions they’re not effective treatments for more advanced infections.  Your best bet: Heading to your doctor or a urology specialist for urine tests that can diagnose a UTI and guide antibiotic treatment. “Delaying treatment could make the infection worse or lead to complications, like a kidney infection,” Dr. Dasgupta cautions. “It’s better to act quickly if the symptoms don’t ease up.” For dehydration, drink more water When you’re dehydrated, your urine becomes more concentrated. “This concentration increases the levels of waste products like urea and creatinine, which can cause the urine to appear cloudy,” Dr. Dasgupta explains. Along with cloudy pee, dehydration may cause symptoms like dark yellow or amber-colored urine, a dry mouth, fatigue, dizziness and infrequent urination. Symptoms such as dizziness and confusion can signal severe dehydration that calls for immediate medical attention and IV fluid replacement, adds Aleece Fosnight, PA-C, medical advisor to Aeroflow Urology and board-certified physician assistant .  But Dr. Dasgupta notes that drinking more water can help correct cloudiness caused by milder cases. “Aiming for at least eight cups (about two liters) of water a day is a good rule of thumb, though individual needs may vary,” he says. “The key is to stay well-hydrated throughout the day, which helps keep urine clear and reduces cloudiness.” For a vaginal infection, try a prescription antibiotic or antifungal  “A bacterial infection known as bacterial vaginosis (BV) and yeast infections are among the most common causes of vaginal infections that could lead to cloudy urine,” notes Dr. Dasgupta. “Both conditions are fairly common and can cause noticeable changes in vaginal discharge.” The discharge then mixes with urine to produce cloudiness.  Other clues that a vaginal infection is your cloudiness culprit: “For BV, you might notice a thin, grayish discharge with a fishy smell, along with mild itching or irritation,” Dr. Dasgupta explains. “Yeast infections, on the other hand, usually come with thick, white discharge (like cottage cheese), intense itching and redness.”  If you experience cloudy pee along with the symptoms above, visit your doctor. “While these infections aren’t usually serious, getting the right treatment can help you feel better faster and avoid complications,” Dr. Dasgupta assures. “For BV, antibiotics are typically prescribed, and yeast infections are treated with antifungal medications, either as a cream, vaginal suppository or pill. Most infections clear up within a few days to a week once treatment begins.” For kidney stones, up your fluid intake Kidney stones trigger cloudy pee through two major mechanisms. “One is the kidney stone itself may cause a urinary tract infection that makes urine cloudy,” Fosnight explains. “Two, the kidney stone typically develops from minerals and crystals, which causes cloudiness of the urine secondary to the increased particle concentration.” Cloudiness due to kidney stones can also be accompanied by changes in urine color, especially redness due to hematuria or blood in urine, adds Fosnight. Other symptoms she cites: Flank pain, nausea, vomiting, fever, chills, urinary frequency and/or urgency, dysuria (pain or burning with urination), malodorous urine and decreased urine output. If you experience such symptoms, Fosnight recommends seeing a medical professional who can conduct a CT scan that evaluates the abdomen and pelvis. If kidney stones are detected, treatment differs depending on their size.  “If the stone is 5 mm or less, individuals are typically able to pass them on their own with increased fluids and alpha blocker medications (like Flomax) to help dilate the ureter and ease the passage,” she says. “For stones 5 mm or larger or smaller stones that are not passing on their own, surgical intervention with ureteroscopy (a scope that goes through the ureter) and/or lithotripsy may be required.” For high blood sugar, visit your doctor Normally, your kidneys filter and reabsorb glucose back into the bloodstream. But when blood sugar levels get too high, the kidneys can’t keep up and the extra glucose ends up in your urine. This is a condition called glucosuria that can make pee cloudy, Dr. Dasgupta explains. “Along with cloudy urine, glucosuria can cause a sweet or fruity smell in your pee,” he says. “You might also notice symptoms like excessive thirst, frequent urination or feeling unusually tired—common signs of elevated blood sugar. Infections like UTIs are also more likely in this scenario.” Your best course of action If you think your cloudy pee is related to high blood sugar: Head to your doctor as soon as possible. “Doctors diagnose glucosuria using a simple urine test, often alongside blood tests to confirm high glucose levels and check overall health,” Dr. Dasgupta notes. “Treatment focuses on managing blood sugar, which might include lifestyle changes, medications or insulin, depending on your condition.” This content is not a substitute for professional medical advice or diagnosis. Always consult your physician before pursuing any treatment plan.   Source link
0 notes
ellajme0 · 3 months ago
Photo
Tumblr media
Ideally, your urine should be pale yellow and clear. But if you’ve ever noticed it appears milky or hazy, you may be wondering, “Why is my pee cloudy?” While cloudy pee can be alarming, there’s good news to report: “Cloudy urine is often linked to a few different factors, and it’s not always something to worry about, “ assures Raj Dasgupta, MD, Chief Medical Advisor for Garage Gym Reviews. “Most of the time, once the cause is identified, clearing up cloudy urine can be fairly simple.” Here, we break down what causes cloudy pee, along with the best ways to treat it. Why is my pee cloudy? 5 causes and cures Some of the most common culprits behind cloudy urine include: For a UTI, sip cranberry juice “Urinary tract infections (UTIs) are one of the most common causes of cloudy urine,” says Dr. Dasgupta. “They bring in white blood cells, bacteria and mucus, which can make the urine look cloudy.”  Cloudy urine from a UTI usually comes with other symptoms like a burning sensation when you pee, a constant need to go (even if it’s just a little) and a lower abdominal ache, he adds. “You might also notice a strong, unpleasant smell or even blood in the urine if the infection is more advanced.” Natural remedies like cranberry juice, cranberry supplements or d-mannose can be helpful for easing the discomfort associated with mild UTIs. (See our round-up of the best doctor-backed home remedies for a UTI here.) But Dr. Daguspta cautions they’re not effective treatments for more advanced infections.  Your best bet: Heading to your doctor or a urology specialist for urine tests that can diagnose a UTI and guide antibiotic treatment. “Delaying treatment could make the infection worse or lead to complications, like a kidney infection,” Dr. Dasgupta cautions. “It’s better to act quickly if the symptoms don’t ease up.” For dehydration, drink more water When you’re dehydrated, your urine becomes more concentrated. “This concentration increases the levels of waste products like urea and creatinine, which can cause the urine to appear cloudy,” Dr. Dasgupta explains. Along with cloudy pee, dehydration may cause symptoms like dark yellow or amber-colored urine, a dry mouth, fatigue, dizziness and infrequent urination. Symptoms such as dizziness and confusion can signal severe dehydration that calls for immediate medical attention and IV fluid replacement, adds Aleece Fosnight, PA-C, medical advisor to Aeroflow Urology and board-certified physician assistant .  But Dr. Dasgupta notes that drinking more water can help correct cloudiness caused by milder cases. “Aiming for at least eight cups (about two liters) of water a day is a good rule of thumb, though individual needs may vary,” he says. “The key is to stay well-hydrated throughout the day, which helps keep urine clear and reduces cloudiness.” For a vaginal infection, try a prescription antibiotic or antifungal  “A bacterial infection known as bacterial vaginosis (BV) and yeast infections are among the most common causes of vaginal infections that could lead to cloudy urine,” notes Dr. Dasgupta. “Both conditions are fairly common and can cause noticeable changes in vaginal discharge.” The discharge then mixes with urine to produce cloudiness.  Other clues that a vaginal infection is your cloudiness culprit: “For BV, you might notice a thin, grayish discharge with a fishy smell, along with mild itching or irritation,” Dr. Dasgupta explains. “Yeast infections, on the other hand, usually come with thick, white discharge (like cottage cheese), intense itching and redness.”  If you experience cloudy pee along with the symptoms above, visit your doctor. “While these infections aren’t usually serious, getting the right treatment can help you feel better faster and avoid complications,” Dr. Dasgupta assures. “For BV, antibiotics are typically prescribed, and yeast infections are treated with antifungal medications, either as a cream, vaginal suppository or pill. Most infections clear up within a few days to a week once treatment begins.” For kidney stones, up your fluid intake Kidney stones trigger cloudy pee through two major mechanisms. “One is the kidney stone itself may cause a urinary tract infection that makes urine cloudy,” Fosnight explains. “Two, the kidney stone typically develops from minerals and crystals, which causes cloudiness of the urine secondary to the increased particle concentration.” Cloudiness due to kidney stones can also be accompanied by changes in urine color, especially redness due to hematuria or blood in urine, adds Fosnight. Other symptoms she cites: Flank pain, nausea, vomiting, fever, chills, urinary frequency and/or urgency, dysuria (pain or burning with urination), malodorous urine and decreased urine output. If you experience such symptoms, Fosnight recommends seeing a medical professional who can conduct a CT scan that evaluates the abdomen and pelvis. If kidney stones are detected, treatment differs depending on their size.  “If the stone is 5 mm or less, individuals are typically able to pass them on their own with increased fluids and alpha blocker medications (like Flomax) to help dilate the ureter and ease the passage,” she says. “For stones 5 mm or larger or smaller stones that are not passing on their own, surgical intervention with ureteroscopy (a scope that goes through the ureter) and/or lithotripsy may be required.” For high blood sugar, visit your doctor Normally, your kidneys filter and reabsorb glucose back into the bloodstream. But when blood sugar levels get too high, the kidneys can’t keep up and the extra glucose ends up in your urine. This is a condition called glucosuria that can make pee cloudy, Dr. Dasgupta explains. “Along with cloudy urine, glucosuria can cause a sweet or fruity smell in your pee,” he says. “You might also notice symptoms like excessive thirst, frequent urination or feeling unusually tired—common signs of elevated blood sugar. Infections like UTIs are also more likely in this scenario.” Your best course of action If you think your cloudy pee is related to high blood sugar: Head to your doctor as soon as possible. “Doctors diagnose glucosuria using a simple urine test, often alongside blood tests to confirm high glucose levels and check overall health,” Dr. Dasgupta notes. “Treatment focuses on managing blood sugar, which might include lifestyle changes, medications or insulin, depending on your condition.” This content is not a substitute for professional medical advice or diagnosis. Always consult your physician before pursuing any treatment plan.   Source link
0 notes
nursingwriter · 27 days ago
Text
Critical Pathway: Chronic Renal Failure Advanced Pathophysiology Regents Online Degree Program Critical Pathway: Chronic renal failure Chronic renal failure is often occasioned by chronic kidney disease, immune disorder, trauma among other conditions. It does not have any specific symptoms and might include feeling unwell generally and experiencing a reduced appetite. It is diagnosed following screening of individuals who are identified to be at risk of kidney problems, like individuals with diabetes or high blood pressure and others who have blood relative with chronic kidney disease. It always seems complex when trying to come up with the right diagnosis for a patient. M.A. is a 60-year-old man who has a stage V chronic kidney disease mainly as a result of diabetic nephropathy and a 12-year of type 2 diabetes. He has symptomatic peripheral vascular insufficiency, and 3 years ago he had undergone coronary artery bypass 3. Within the ten months that passed, Mr. M.A. had been undergoing hemodialysis 3 days in a week for 3.5 hours via left arm arteriovenous fistula. For the last 3 days he had undergone dialysis following his scheduled dialysis on the day of visit. Three months before Mr. M.A. was admitted, he had developed a non-healing left foot ulcer and a critical lower limb ischemia. Several attempts such as vascular intervention to restore sufficient limb blood flow did not produce a positive result, and after two-month he had to undergo a transmetatarsal amputation. After the surgery the patient found that he was developing surgical wound infection, which called for a repeated debridement as well as intravenous vancomycin administration. According to his wife Mr. M.A. was also showing some signs of continuous confusion and had been having visual hallucinations, claiming to be seeing things that never existed in real life. Such signs began some 2 weeks before he was admitted as an intermittent episode. However, the wife could identify any triggering events or temporal pattern for the episodes. Some 2 days which have passed these signs have been more persistent. Such confusion had never been seen from Mr. M.A. As much he was somehow forgetful in the previous years he was still able to take care of himself and perform simple tasks. As a patient he was receiving medication of atorvastatin, atenolol, aspirin, gabapentin, insulin and the recent medication was vancomycin. For several years the patient had been taking 300mg of gabapentin 4 times in a day and this was effectively controlling his diabetic neuropathic pain. Administering of vancomycin was done during hemodialysis as per the blood levels. His wife made sure that he followed his mediation and dialysis regime strictly. Physical Examination Mr M.A. was somnolent and a febrile but arousable. Some of his critical signs included: Height- 4 feet Weight- 120 lbs Pulse rate of 60 beats/min (regular). Blood pressure of 138/88 mm Hg Respiration rate of 14 breaths/min Temperatures 98.1 (oral) Oxygen saturation while breathing room air of 98% Left metatarsal stump wound was healing Euvolemic without pericardial rubs Waking up periodically Lab results included the following: Abnormal Normal Hemoglobin 11.1 g/dL 13.5-17.5 g/dL White blood cells 5.7 x 109/L 3.5 -- 109/L Platelets 225 x 109/L 150-450 X 109/L Potassium 5.3mEq/L 3.6-4.8mEq/L Sodium 140 mEq/L 135-145 mEq/L Chloride 103 mEq/L 100-108 mEq/L Bicarbonate 20 mEq/L 22-29 mEq/L Glucose 130 mg/dL 70-100 mg/dL Creatinine 5.1 mg/dL 0.8-1.3 mg/dL Blood urea nitrogen 50 mg / dL 8-24 mg/dL When head MRI was done it revealed mild brain atrophy without mass lesion, hemorrhage, or ischemia. Revelation of electroencephalography was that nonepileptogenic, mild bitemporal slowing. Mr. M.A. was put on a full dialysis session, and 2 hours after dialysis as well as prior to dosing, the level of gabapentin were 27.0 ?g/Ml. This is due to the fact that circulating gabapentine is an eliminating efficiency at the time of dialysis. Such a level shows the tissue rebound and reveals that the predialysis level of this patient was clearly elevated. Assessment Causes of the Patient's altered mental status Patients with multiple comorbid conditions are at risk of altered mental status and it can be facilitated by various acute illnesses. Sometimes, it can be the sole symptoms of systemic infection. Consequently, some of the infections like urinary tract infections and pneumonia is suppose to be included within the differential diagnosis and then ruled out. But Mr. M.A. was a febrile, did not have urinary or respiratory symptoms, and was just recently when he was treated with antibiotic. Meaning that it is not likely that infection was the cause of these problems. Stroke is known to be associated with hallucinations and intermittent symptoms of altered mental status, particularly when there are no focal neurologic deficits, implying that it is not likely for stroke to be the cause of these problems. Parkinson-like motor disorder or Parkinson disease is associated with Lewy Body Dementia (LBD). Those patients who are experiencing LBD use to show complex hallucinations and fluctuations in alertness in people. It is known that hallucinations may bring a movement disorder and dementia. As much as LBD may seem to be consistence with the problem of Mr. M.A., the sudden start as well as fast progression would be extremely uncharacterized in LBD, ruling out its possibility. Following Mr. M.A. having history of adherence to regular dialysis in addition to non-presence of uremia's physical signs indicate that hallucinations and decrease alertness are not a result of uremia. Again, during initiation of dialysis he was uremic but failed to demonstrate the same symptoms. It is important to note that in recent weeks, the patient was given multiple agents such as contrast agents for computed tomography and magnetic resonance plus postoperative and preoperative antibiotics. Therefore, the potential and likely cause of the patient's problem could have been medication toxicity, particularly in the setting of renal failure. On the day of his admission, the patient underwent dialysis, and there was an immediate improvement of his hallucinations but came back again during the dialysis sessions. Discussion Mr. M.A. has been known to have Type 2 diabetes which is a chronic condition that always affects the manner in which the body of a person metabolizes glucose (sugar), which is the main source of fuel. It was once known as non-insulin dependent diabetes or an adult-onset. When a person is diagnosed with type 2 diabetes, it means that the body either is failing to produce enough insulin that helps in maintaining a normal glucose level, or the body is resisting the effects of insulin (a hormone that helps in regulating the movement of sugar into the body cell), (Ahern J, Kruger DF., 1989). Though the condition is untreatable, it can be managed by eating well, doing exercises as well as maintaining a healthy weight. Following continuous changes that are taking place within the health care system as well as public policy, there has been a shift in the treatment of renal chronic related acute settings like hospitals, towards outpatient managed care organizations and facilities. The need to achieve a cost-effective treatment is on the rise. Health care professionals specializing in the care of people with renal chronic and other similar illnesses are increasingly being recognized as an important group even in the manner in which they carefully attend to these patients. In the attempt to promote health and prevent occurrence of these related disorders, the health care provider have realized the need for self-management. The patients as well as those who take care of them are trained and educated on how to manage themselves or those who they take care of without necessarily having to visit health facility everyday. Mr. M.A. has also undergone surgery, has wound infection and undergone dialysis. What provided clues for active infection and do away with substantial electrolyte abnormalities and hypoglycemia was an electrolyte panel with measurement concentration of glucose as well as a CBC. Even though there was unlikely of seizure following the history of the patient, useful corroborative information could be based on electroencephalography. MRI of the head can be used to evaluate structural abnormalities like mass lesion and brain atrophy. Elimination of gabapentin takes place from the urine, and accumulates in blood if you are a patient with renal failure. When gabapetin is excessively accumulated it may cause different neurologic toxicities, such as coma and hallucination. Therefore the level of gabapentin should be obtained. It would be of little help to consider arterial blood gas since the patient does not manifest respiratory signs and symptoms of oxygen saturation and labored breathing when the breathing room air was 98%. Generally, gabapentine is usually well absorbed and has not been identified to exhibit batch-to-batch variations in it bioavailability. While in the blood stream, it is not bound by protein, (Luer MS, Hamani C, Dujovny M, et al. (1999). Therefore having co-administered medications that tend to bind serum protein is not supposed to have an effect on the gabapentin circulation level. Since gabapentin is usually not metabolized hepatically, it should not be affected by variations of the hepatic cytochrome system activities and any of the effects it has is not inhibited or induced by co-administered hepatic medications, (Blum RA, Comstock TJ, Sica DA, et al., 1994). As a result, it is unlikely that pharmacokinetic or molecular drug-drug interactions accounts for accumulation of gabapentin. Mr. M.A. has been following his prescribed medication and any form of acute overdosing has not been revealed by either him or his wife. Gabapentin is excreted renaly. Reducing the capacity of renal excretion may in turn rise up the blood level of gabapentin, eliciting neurologic symptoms, as was indicated before. The patient had previously started undergoing dialysis and the expectation to achieve a substantial residual renal clearance, (Spafford JD, Zamponi GW., 2003). But, since there was a repeated exposure of the patient to intravenous contrast agent for limb ischemia evaluation, might have eradicated his residual clearance, resulting to accumulation of gabapentin. In the past several months, Mr. M.A. has been adhering to the dialysis regime, and the delivered dialysis has been adequate. Therefore, the issue of inadequate dialysis is not likely to be the man inciting factor. When the patient was questioned further, he admitted that he had a progressive decline in urine output and almost anuric at the time of admission. Due to the loss of residual kidney function might have been the caused by the increasing gabapentin accumulation. Risk factors A consideration can be on ?-Blocker since they have been known to slow down the release of certain adrenergic neurotransmitters. Yet, it is generally thought that analgesic effect of gabapentin lie in the blockage of presynaptic release of neurotransmitters, as well as serontonin, norepinephrine, and acetylcholine. It is not known that ?-blockers alter gabapentin's effect. Most of the patient for many years has been taking gabapentin and atenolol concurrently without apparently realizing any toxic. Even with the actively transportation of gabapentin to brain tissues, there have not been signs of atherosclerotic vascular changes to alter the pattern of its distribution or diminishing its entry to brain tissue, (Wong MO, Eldon MA, Keane WF, et al.(1995). It has remained effective for controlling pain in patients who have severe atherosclerotic vascular disease. The major cause of kidney failure of Mr. M.A was diabetic nephropathy. On the other hand, diabetic nephropathy has not been known to bring forth a prediction for gabapentin-induced neurotoxicity, as well as hallucinations, over the rest of kidney failure causes. Gabapentin inhibiting presynaptic Ca 2+ influx tend to be the main putative mechanism leading to the desired effects of analgesic, (Catterall WA., 2000). This mechanism may account for the fundamental neurotoxicity causes. Severe, mild, or dementia tends to be associated with an augmented incidents of gabapentin-induced changes within the mental status, (Dogukan A, Aygen B, 2006). For patients who happens to have mild dementia, the evidence shows that gabapentin worsen dramatically the neuropsychiatric disturbances, resulting to a complex dominated psychoagitation through persistent hallucinations and ideas of reference. Since Mr. M.A. is having loss of memory, indicating some signs of dementia, a condition might have been the one that landed him to neuropsychiatric symptoms that was triggered by gabapentin toxicity. Interventions An individual with normal kidney clearance will have a kidney that excretes gabapentin with a half life of 5 to 7 hours. For patients who are experiencing a reduced kidney function, the increase of their half-life is up to 132 hours without dialysis. Dosing range for gabapentin patients experiencing chronic kidney dysfunction from stage III to V is always 100 to 1400 mg/d. But, dosing should be further raised for individual patients based on the level of kidney failure as well as the estimated drug half-life.Gabapentin's tissue content tend to be linearly proportional to the blood level, and there is effective removal of circulating gabapentin by hemodialysis. When the dosage is reduced while dosage frequently remains may lead to an initial sub-therapeutic drug level once the dialysis and a supratherapeutic level has been carried out before the next session of dialysis. Consequently, it is not appropriate to cut just down the dosage such as by 100 mg 3 times daily. The dosage is supposed to be reduced by frequency of 300 mg once a dialysis has been carried out and this maintains sufficient blood level, and this is what Mr. M.A. needs. Since he was experiencing neuropathic pain, gabapentin should be used in controlling the pain. Central nervous system depression secondary to benzodiazepines will be reversed by Flumazenil. It has been known for treatment of gabapentin toxicity, (Raudino F, Mascalzi MG, Zagami A., 2004). Mr. M.A. received a measure by withholding gabapentin for a day and reinintitiated at 300 mg after 3 times per week. As a result the level of his predialysis gabapentin went down to 16.6 ?g/mL, thereby restoring his mental baseline. Discussion The case of Mr. M.A. is an example of complexity experienced when caring for patients with chronic kidney disease as well as multiple comorbid conditions. It shows how a devastating toxicity may take place with what one may consider to be a well-tolerated medication; which can even be at the reference dosing range. Chronic kidney failure is well-known global epidemic, and among the main causes is diabetes, (Coresh J, Selvin E, Stevens LA, et al., 2007). Those who are suffering form diabetes and nephropathy tend to display a common concurrent diabetic neuropathy. Palliating of neuropathic pain has been frequently done by gabapentin. In United States gabapentin became released in 1993 to act as an anticonvulsant agent. Several clinical and preclinical trials across different states, has identified gabapentin to be a well tolerated and effective anticonvulsant agent and also anxiolytic as well as analgesic agent, (Rossi P, Serrao M, Pozzessere G., 2002). Recently, its use has increasingly been off-label for expanded indications, such as diabetic neuropathy, hot flashes, uremic pruritus, and phantom limb pain. An analogue of ?-aminobutyric acid (C9H17NO2) and a water-soluble 1-(aminomethyl)-cyclohexaneacetic acid crosses readily the blood brain barrier and transported actively into the brain tissues through system L. It is shown that the concentration of gabapentin in brain tisues is the same as or higher than the one in blood, (Brawek B, Loffler M, 2008). Even though the experimental data shows that gabapentin mediates analgesia through presynaptic VSCC inhibition, those who investigate have again discovered the existence of lower well-defined, "2"-1 -- mediated regulatory pathways, that is independed to the functions of VSCC. Therefore, there has not been a fully elucidated complete effect of spectrum of gabapentin-mediated pharmacologic and toxicologic. In addition, under physiologic conditions, gabapentin usually shows minimal effects, however, it clearly alters synaptic neurotransmitter's profile at the time of neuronal hyperexcitability. Hence, end results in patients who experience functional and structural alterations of the brain. Gabapentin that is absorbed well from the gastrointestinal tract, tend to have a consistent of 50% to 60% bioavailability, and is not altered in those with kidney dysfunction. While circulating, it has not been bound by metabolized or protein. Even though a target degree of blood has not been defined, 8 to 20 ?g/mL has found to have a correlation with clinical efficiency, (Wen CP, Cheng TY, Tsai MK, et al., 2008). Elimination of gabapentin in urine is at arate which is proportional to clearance of creatinine. Therefore, with preserved gastrointestinal absorption and progressive kidney failure, diminishing kidney elimination can create a considerable gabapentin toxicity risk. A clue to the diagnosis Mr. M.A. may have been manifested by the transient improvement in mental status immediately after hemodialysis. This is due to the fact that gabapentin can be dialyzed readily, for example a post dialysis level of 26.4 ?g/mL could predict a highly increased predialysis level in at least the mid 40s. Some other clue to potential gabapentin toxicity may have been the reduction of urine output that resulted to the onset of neurologic symptoms, (Bassilios N, Launay-Vacher V, 2001). Many of the patients for along time have been given similar dosage of gabapentin without manifestations of neurologic. Such a possibility was evident after there was a decrease of predialysis gabapentin to the required level after the dose was reduced. At the same time the patient regained his mental alertness and there were no more hallucinations. Conclusion There are many points to be deduced from this case. Residual kidney function is essential for patients who are receiving long-term dialysis and when a patient experience loss of residual function, it may result to a very serious clinical outcome, moreover it is supposed to be considered in formulating a diagnosis; A well tolerated medication with an excellent pharmacokinetic profile is capable of causing an overwhelming and potentially life-threatening toxicities; Those patients who are experiencing initial dementia are at risk of having mental status alteration following system disorder, as well as drug toxicity; Even within the general reference dosing range, still medication toxicity may occur in patients with kidney failure. The patient patients use to receive an inappropriately high dosage of gabapentin even prior to the loss of residual kidney clearance. The patient's residual kidney clearance seems to have barred him from developing overt toxicity. Therefore, it is of importance for tailoring of drug dosing to these patients and be followed by a continuous monitoring. Medical care for patients who are elderly and experience kidney dysfunction as well as multiple comorbid conditions has increasingly become complex and challenging. Undertaking delicate changes within the baseline of functional organ is capable of having a dramatic effect to the patient's response to treatment. However, by taking these complexities into consideration will prevent excessive investigative work-ups as well as improve the quality of our healthcare services. Read the full article
0 notes
bharathomoeopathy · 24 days ago
Text
Effective and Natural Treatment for Kidney Failure – A Comprehensive Guide by Bharat Homeopathy
Introduction
Kidney diseases are among the most common health concerns worldwide. Millions of people suffer from kidney-related problems, leading to serious complications such as kidney failure. Traditional medical treatments, including dialysis and kidney transplants, often come with risks and lifelong dependency. However, alternative treatments, such as homeopathy, offer a natural and effective way to manage kidney diseases. At Bharat Homeopathy, we provide holistic solutions to help patients improve kidney function and reduce dependency on dialysis. This blog explores various aspects of treatment for kidney failure, possibilities of a cure for chronic kidney disease, the role of kidney problem medication, and the best chronic kidney disease treatment available today. Additionally, we will discuss kidney failure treatment without dialysis and high creatinine treatment options.
Tumblr media
Understanding Kidney Disease
Kidneys play a vital role in filtering waste, balancing body fluids, and regulating blood pressure. When kidney function declines, toxins build up in the body, leading to severe health problems.
Types of Kidney Disease
Chronic Kidney Disease (CKD): A progressive condition where kidney function declines over time.
Acute Kidney Failure: A sudden loss of kidney function due to infection, dehydration, or injury.
End-Stage Kidney Disease (ESKD): The final stage of CKD, where the kidneys fail completely.
Early detection and proper chronic kidney disease treatment can help slow the progression and prevent complications.
Best Treatment for Kidney Failure
1. Conventional Approaches
Dialysis: Helps remove waste when kidneys can no longer function properly.
Kidney Transplant: Involves replacing a damaged kidney with a healthy donor kidney.
While these methods are widely used, they often lead to side effects, infections, and dependency on lifelong medications. Many patients now seek kidney failure treatment without dialysis, which is where homeopathy plays a crucial role.
2. Homeopathic Treatment for Kidney Failure
At Bharat Homeopathy, we offer natural remedies to stimulate kidney function and reduce the need for dialysis. Homeopathic medicines improve kidney filtration, lower creatinine levels, and restore overall kidney health. Some effective remedies include:
Apis Mellifica: Reduces swelling and water retention.
Berberis Vulgaris: Supports kidney function and reduces pain.
Serum Anguillae: Helps lower creatinine and urea levels.
Arsenicum Album: Useful for patients experiencing severe weakness and fatigue.
Our personalized treatment plans focus on eliminating the root cause rather than just controlling symptoms.
Cure for Chronic Kidney Disease – Is It Possible?
While conventional medicine claims that CKD has no cure, homeopathy offers a holistic approach to slowing progression and, in some cases, reversing early-stage kidney damage. At Bharat Homeopathy, our treatments aim to: ✔ Strengthen kidney function naturally. ✔ Reduce dependency on dialysis. ✔ Improve overall health and immunity. ✔ Prevent further kidney damage.
Key Strategies for CKD Management
Dietary Changes: Reduce sodium, phosphorus, and potassium intake while maintaining hydration.
Herbal Remedies: Herbs like Punarnava, Gokhru, and Varun help detoxify the kidneys.
Homeopathic Medicines: Work on the root cause rather than just controlling symptoms.
Lifestyle Modifications: Regular exercise, stress management, and avoiding smoking and alcohol.
Our homeopathic approach ensures that patients receive a customized chronic kidney disease treatment plan that suits their individual health needs.
Kidney Problem Medication – Natural & Safe Alternatives
Most conventional kidney problem medication includes diuretics, blood pressure drugs, and medications to manage complications like anemia and bone disease. However, prolonged use of these medications can have harmful side effects.
Homeopathic Kidney Medications
Homeopathic remedies provide a safe alternative to chemical-based medications. Some effective treatments include:
Cantharis: Helps relieve burning sensations and urinary discomfort.
Terebinthina: Useful in reducing protein leakage in urine.
Solidago: Helps in reducing kidney inflammation and improving urine output.
Kidney Failure Treatment Without Dialysis – A Natural Approach
Many patients look for ways to manage kidney failure without undergoing dialysis. Homeopathy offers a promising kidney failure treatment without dialysis, focusing on natural healing and kidney regeneration.
Benefits of Homeopathic Treatment Without Dialysis:
✔ Reduces creatinine and urea levels. ✔ Enhances kidney filtration capacity. ✔ Eliminates toxins naturally. ✔ Improves overall health without invasive procedures.
If you’re searching for an alternative to dialysis, Bharat Homeopathy provides a natural and effective solution to manage kidney disease.
High Creatinine Treatment – How to Lower Creatinine Naturally
Creatinine is a waste product produced by muscle metabolism. High levels indicate impaired kidney function. High creatinine treatment involves a combination of homeopathy, diet, and lifestyle changes.
Natural Ways to Lower Creatinine:
Increase Water Intake: Helps flush out toxins.
Reduce Protein Consumption: Too much protein increases creatinine levels.
Avoid Processed Foods: High in phosphorus and sodium, which can worsen kidney damage.
Homeopathic Remedies: Such as Serum Anguillae and Solidago, which help in detoxifying the kidneys naturally.
At Bharat Homeopathy, our treatment plans focus on reducing creatinine levels safely without causing side effects.
Why Choose Bharat Homeopathy?
At Bharat Homeopathy, we believe in providing natural, personalized, and effective treatments for kidney diseases. Our key benefits include: ✔ Customized treatment plans tailored to individual patient needs. ✔ Reduction in dependency on dialysis and harmful medications. ✔ Holistic approach that treats the root cause of kidney disease. ✔ Safe, side-effect-free homeopathic remedies. ✔ Experienced professionals providing continuous guidance and support.
Final Thoughts
Kidney disease is a serious condition that requires timely and effective management. Whether you are looking for the best treatment for kidney failure, a possible cure for chronic kidney disease, natural kidney problem medication, or alternative chronic kidney disease treatment, homeopathy offers a promising solution. Additionally, if you want a kidney failure treatment without dialysis or need high creatinine treatment, Bharat Homeopathy provides safe, natural, and effective remedies tailored to your health needs.
If you or a loved one is suffering from kidney disease, don’t wait! Contact Bharat Homeopathy today for a consultation and start your journey to better kidney health.
0 notes
chilimili212 · 3 months ago
Photo
Tumblr media
Ideally, your urine should be pale yellow and clear. But if you’ve ever noticed it appears milky or hazy, you may be wondering, “Why is my pee cloudy?” While cloudy pee can be alarming, there’s good news to report: “Cloudy urine is often linked to a few different factors, and it’s not always something to worry about, “ assures Raj Dasgupta, MD, Chief Medical Advisor for Garage Gym Reviews. “Most of the time, once the cause is identified, clearing up cloudy urine can be fairly simple.” Here, we break down what causes cloudy pee, along with the best ways to treat it. Why is my pee cloudy? 5 causes and cures Some of the most common culprits behind cloudy urine include: For a UTI, sip cranberry juice “Urinary tract infections (UTIs) are one of the most common causes of cloudy urine,” says Dr. Dasgupta. “They bring in white blood cells, bacteria and mucus, which can make the urine look cloudy.”  Cloudy urine from a UTI usually comes with other symptoms like a burning sensation when you pee, a constant need to go (even if it’s just a little) and a lower abdominal ache, he adds. “You might also notice a strong, unpleasant smell or even blood in the urine if the infection is more advanced.” Natural remedies like cranberry juice, cranberry supplements or d-mannose can be helpful for easing the discomfort associated with mild UTIs. (See our round-up of the best doctor-backed home remedies for a UTI here.) But Dr. Daguspta cautions they’re not effective treatments for more advanced infections.  Your best bet: Heading to your doctor or a urology specialist for urine tests that can diagnose a UTI and guide antibiotic treatment. “Delaying treatment could make the infection worse or lead to complications, like a kidney infection,” Dr. Dasgupta cautions. “It’s better to act quickly if the symptoms don’t ease up.” For dehydration, drink more water When you’re dehydrated, your urine becomes more concentrated. “This concentration increases the levels of waste products like urea and creatinine, which can cause the urine to appear cloudy,” Dr. Dasgupta explains. Along with cloudy pee, dehydration may cause symptoms like dark yellow or amber-colored urine, a dry mouth, fatigue, dizziness and infrequent urination. Symptoms such as dizziness and confusion can signal severe dehydration that calls for immediate medical attention and IV fluid replacement, adds Aleece Fosnight, PA-C, medical advisor to Aeroflow Urology and board-certified physician assistant .  But Dr. Dasgupta notes that drinking more water can help correct cloudiness caused by milder cases. “Aiming for at least eight cups (about two liters) of water a day is a good rule of thumb, though individual needs may vary,” he says. “The key is to stay well-hydrated throughout the day, which helps keep urine clear and reduces cloudiness.” For a vaginal infection, try a prescription antibiotic or antifungal  “A bacterial infection known as bacterial vaginosis (BV) and yeast infections are among the most common causes of vaginal infections that could lead to cloudy urine,” notes Dr. Dasgupta. “Both conditions are fairly common and can cause noticeable changes in vaginal discharge.” The discharge then mixes with urine to produce cloudiness.  Other clues that a vaginal infection is your cloudiness culprit: “For BV, you might notice a thin, grayish discharge with a fishy smell, along with mild itching or irritation,” Dr. Dasgupta explains. “Yeast infections, on the other hand, usually come with thick, white discharge (like cottage cheese), intense itching and redness.”  If you experience cloudy pee along with the symptoms above, visit your doctor. “While these infections aren’t usually serious, getting the right treatment can help you feel better faster and avoid complications,” Dr. Dasgupta assures. “For BV, antibiotics are typically prescribed, and yeast infections are treated with antifungal medications, either as a cream, vaginal suppository or pill. Most infections clear up within a few days to a week once treatment begins.” For kidney stones, up your fluid intake Kidney stones trigger cloudy pee through two major mechanisms. “One is the kidney stone itself may cause a urinary tract infection that makes urine cloudy,” Fosnight explains. “Two, the kidney stone typically develops from minerals and crystals, which causes cloudiness of the urine secondary to the increased particle concentration.” Cloudiness due to kidney stones can also be accompanied by changes in urine color, especially redness due to hematuria or blood in urine, adds Fosnight. Other symptoms she cites: Flank pain, nausea, vomiting, fever, chills, urinary frequency and/or urgency, dysuria (pain or burning with urination), malodorous urine and decreased urine output. If you experience such symptoms, Fosnight recommends seeing a medical professional who can conduct a CT scan that evaluates the abdomen and pelvis. If kidney stones are detected, treatment differs depending on their size.  “If the stone is 5 mm or less, individuals are typically able to pass them on their own with increased fluids and alpha blocker medications (like Flomax) to help dilate the ureter and ease the passage,” she says. “For stones 5 mm or larger or smaller stones that are not passing on their own, surgical intervention with ureteroscopy (a scope that goes through the ureter) and/or lithotripsy may be required.” For high blood sugar, visit your doctor Normally, your kidneys filter and reabsorb glucose back into the bloodstream. But when blood sugar levels get too high, the kidneys can’t keep up and the extra glucose ends up in your urine. This is a condition called glucosuria that can make pee cloudy, Dr. Dasgupta explains. “Along with cloudy urine, glucosuria can cause a sweet or fruity smell in your pee,” he says. “You might also notice symptoms like excessive thirst, frequent urination or feeling unusually tired—common signs of elevated blood sugar. Infections like UTIs are also more likely in this scenario.” Your best course of action If you think your cloudy pee is related to high blood sugar: Head to your doctor as soon as possible. “Doctors diagnose glucosuria using a simple urine test, often alongside blood tests to confirm high glucose levels and check overall health,” Dr. Dasgupta notes. “Treatment focuses on managing blood sugar, which might include lifestyle changes, medications or insulin, depending on your condition.” This content is not a substitute for professional medical advice or diagnosis. Always consult your physician before pursuing any treatment plan.   Source link
0 notes
oliviajoyice21 · 3 months ago
Photo
Tumblr media
Ideally, your urine should be pale yellow and clear. But if you’ve ever noticed it appears milky or hazy, you may be wondering, “Why is my pee cloudy?” While cloudy pee can be alarming, there’s good news to report: “Cloudy urine is often linked to a few different factors, and it’s not always something to worry about, “ assures Raj Dasgupta, MD, Chief Medical Advisor for Garage Gym Reviews. “Most of the time, once the cause is identified, clearing up cloudy urine can be fairly simple.” Here, we break down what causes cloudy pee, along with the best ways to treat it. Why is my pee cloudy? 5 causes and cures Some of the most common culprits behind cloudy urine include: For a UTI, sip cranberry juice “Urinary tract infections (UTIs) are one of the most common causes of cloudy urine,” says Dr. Dasgupta. “They bring in white blood cells, bacteria and mucus, which can make the urine look cloudy.”  Cloudy urine from a UTI usually comes with other symptoms like a burning sensation when you pee, a constant need to go (even if it’s just a little) and a lower abdominal ache, he adds. “You might also notice a strong, unpleasant smell or even blood in the urine if the infection is more advanced.” Natural remedies like cranberry juice, cranberry supplements or d-mannose can be helpful for easing the discomfort associated with mild UTIs. (See our round-up of the best doctor-backed home remedies for a UTI here.) But Dr. Daguspta cautions they’re not effective treatments for more advanced infections.  Your best bet: Heading to your doctor or a urology specialist for urine tests that can diagnose a UTI and guide antibiotic treatment. “Delaying treatment could make the infection worse or lead to complications, like a kidney infection,” Dr. Dasgupta cautions. “It’s better to act quickly if the symptoms don’t ease up.” For dehydration, drink more water When you’re dehydrated, your urine becomes more concentrated. “This concentration increases the levels of waste products like urea and creatinine, which can cause the urine to appear cloudy,” Dr. Dasgupta explains. Along with cloudy pee, dehydration may cause symptoms like dark yellow or amber-colored urine, a dry mouth, fatigue, dizziness and infrequent urination. Symptoms such as dizziness and confusion can signal severe dehydration that calls for immediate medical attention and IV fluid replacement, adds Aleece Fosnight, PA-C, medical advisor to Aeroflow Urology and board-certified physician assistant .  But Dr. Dasgupta notes that drinking more water can help correct cloudiness caused by milder cases. “Aiming for at least eight cups (about two liters) of water a day is a good rule of thumb, though individual needs may vary,” he says. “The key is to stay well-hydrated throughout the day, which helps keep urine clear and reduces cloudiness.” For a vaginal infection, try a prescription antibiotic or antifungal  “A bacterial infection known as bacterial vaginosis (BV) and yeast infections are among the most common causes of vaginal infections that could lead to cloudy urine,” notes Dr. Dasgupta. “Both conditions are fairly common and can cause noticeable changes in vaginal discharge.” The discharge then mixes with urine to produce cloudiness.  Other clues that a vaginal infection is your cloudiness culprit: “For BV, you might notice a thin, grayish discharge with a fishy smell, along with mild itching or irritation,” Dr. Dasgupta explains. “Yeast infections, on the other hand, usually come with thick, white discharge (like cottage cheese), intense itching and redness.”  If you experience cloudy pee along with the symptoms above, visit your doctor. “While these infections aren’t usually serious, getting the right treatment can help you feel better faster and avoid complications,” Dr. Dasgupta assures. “For BV, antibiotics are typically prescribed, and yeast infections are treated with antifungal medications, either as a cream, vaginal suppository or pill. Most infections clear up within a few days to a week once treatment begins.” For kidney stones, up your fluid intake Kidney stones trigger cloudy pee through two major mechanisms. “One is the kidney stone itself may cause a urinary tract infection that makes urine cloudy,” Fosnight explains. “Two, the kidney stone typically develops from minerals and crystals, which causes cloudiness of the urine secondary to the increased particle concentration.” Cloudiness due to kidney stones can also be accompanied by changes in urine color, especially redness due to hematuria or blood in urine, adds Fosnight. Other symptoms she cites: Flank pain, nausea, vomiting, fever, chills, urinary frequency and/or urgency, dysuria (pain or burning with urination), malodorous urine and decreased urine output. If you experience such symptoms, Fosnight recommends seeing a medical professional who can conduct a CT scan that evaluates the abdomen and pelvis. If kidney stones are detected, treatment differs depending on their size.  “If the stone is 5 mm or less, individuals are typically able to pass them on their own with increased fluids and alpha blocker medications (like Flomax) to help dilate the ureter and ease the passage,” she says. “For stones 5 mm or larger or smaller stones that are not passing on their own, surgical intervention with ureteroscopy (a scope that goes through the ureter) and/or lithotripsy may be required.” For high blood sugar, visit your doctor Normally, your kidneys filter and reabsorb glucose back into the bloodstream. But when blood sugar levels get too high, the kidneys can’t keep up and the extra glucose ends up in your urine. This is a condition called glucosuria that can make pee cloudy, Dr. Dasgupta explains. “Along with cloudy urine, glucosuria can cause a sweet or fruity smell in your pee,” he says. “You might also notice symptoms like excessive thirst, frequent urination or feeling unusually tired—common signs of elevated blood sugar. Infections like UTIs are also more likely in this scenario.” Your best course of action If you think your cloudy pee is related to high blood sugar: Head to your doctor as soon as possible. “Doctors diagnose glucosuria using a simple urine test, often alongside blood tests to confirm high glucose levels and check overall health,” Dr. Dasgupta notes. “Treatment focuses on managing blood sugar, which might include lifestyle changes, medications or insulin, depending on your condition.” This content is not a substitute for professional medical advice or diagnosis. Always consult your physician before pursuing any treatment plan.   Source link
0 notes