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10.1038/sj.ki.5002564

http://scihub22266oqcxt.onion/10.1038/sj.ki.5002564
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17928827!ä!17928827

suck abstract from ncbi


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pmid17928827      Kidney+Int 2007 ; 72 (12): 1483-92
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  • Thiazide-induced subtle renal injury not observed in states of equivalent hypokalemia #MMPMID17928827
  • Reungjui S; Hu H; Mu W; Roncal CA; Croker BP; Patel JM; Nakagawa T; Srinivas T; Byer K; Simoni J; Wesson D; Sitprija V; Johnson RJ
  • Kidney Int 2007[Dec]; 72 (12): 1483-92 PMID17928827show ga
  • Hydrochlorothiazide (HCTZ) is used to manage hypertension and heart failure; however, its side effects include mild hypokalemia, metabolic abnormalities, and volume depletion, which might have deleterious effects on renal and endothelial function. We studied whether HCTZ cause renal injury and/or altered vasoreactivity and if these changes are hypokalemia-dependent. Rats were given a normal diet or a diet moderately low in potassium K+ with or without HCTZ. Animals fed either a low K+ diet alone or HCTZ developed mild hypokalemia. There was no significant difference in systolic blood pressure in the different treatment groups. All three groups with hypokalemia had mild proteinuria; low K(+)-HCTZ rats had reduced creatinine clearance. HCTZ-treated rats displayed hypomagnesemia, hypertriglyceridemia, hyperglycemia, insulin resistance, and hyperaldosteronism. No renal injury was observed in the groups without HCTZ; however, increased kidney weight, glomerular ischemia, medullary injury, and cortical oxidative stress were seen with HCTZ treatment. Endothelium-dependent vasorelaxation was reduced in all hypokalemic groups and correlated with reduced serum K+, serum, and urine nitric oxide. Our results show that HCTZ is associated with greater renal injury for the same degree of hypokalemia as the low K+ diet, suggesting that factors such as chronic ischemia and hyperaldosteronism due to volume depletion may be responsible agents. We also found impaired endothelium-dependent vasorelaxation was linked to mild hypokalemia.
  • |Aldosterone/blood[MESH]
  • |Animals[MESH]
  • |Blood Pressure/drug effects[MESH]
  • |Body Weight[MESH]
  • |Diuretics/*toxicity[MESH]
  • |Hydrochlorothiazide/*toxicity[MESH]
  • |Hypertension, Renal/*drug therapy/metabolism/pathology[MESH]
  • |Hypokalemia/*chemically induced/complications/metabolism[MESH]
  • |Immunohistochemistry[MESH]
  • |Insulin Resistance[MESH]
  • |Insulin/blood[MESH]
  • |Kidney/metabolism/pathology[MESH]
  • |Magnesium/metabolism[MESH]
  • |Male[MESH]
  • |Muscle, Skeletal/metabolism[MESH]
  • |Nitric Oxide/metabolism[MESH]
  • |Organ Size[MESH]
  • |Oxidative Stress/drug effects[MESH]
  • |Potassium, Dietary/blood/pharmacology[MESH]
  • |Proteinuria/etiology/metabolism/pathology[MESH]
  • |Rats[MESH]
  • |Rats, Sprague-Dawley[MESH]
  • |Sodium/metabolism[MESH]
  • |Urine[MESH]


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