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Caloric restriction or telmisartan control dyslipidemia and nephropathy in obese diabetic Zücker rats

机译:肥胖的糖尿病Zücker大鼠的热量限制或替米沙坦控制性血脂异常和肾病

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Background The obese Zücker diabetic fatty male rat (ZDF:Gmi?-fa) is an animal model of type II diabetes associated with obesity and related metabolic disturbances like dyslipidaemia and diabetic nephropathy. In addition, diabetic dyslipidaemia has been linked to vascular and glomerular damage too. Dietary fat restriction is a current strategy to tackle obesity and, telmisartan, as a renoprotective agent, may mediate cholesterol efflux by activating PPARγ. To test the hypothesis that both therapeutical alternatives may influence dyslipidaemia and nephropathy in the ZDF rat, we studied their effect on development of diabetes. Methods Male Zücker Diabetic Fatty (ZDF) rats received a low-calorie diet, vehicle or telmisartan for 9 weeks. Blood samples were obtained for analyses of lipids and lipoproteins, LDL-oxidisability, HDL structural and functional properties. Urinalysis was carried out to estimate albumin loss. At the end of the experimental period, rats were sacrificed, liver extracted and APOA1 mRNA quantified. Results Results indicated that low-calorie diet and telmisartan can slower the onset of overt hyperglycaemia and renal damage assessed as albuminuria. Both interventions decreased the oxidative susceptibility of LDL and hepatic APOA1 mRNA expression but only dietary restriction lowered hyperlipidaemia. Conclusion Either a dietary or pharmacologic interventions with telmisartan have important beneficial effects in terms of LDL oxidative susceptibility and progression of albuminuria in obesity related type II diabetes.
机译:背景技术肥胖的Zücker糖尿病脂肪性雄性大鼠(ZDF:Gmi?-fa)是与肥胖症和相关的代谢障碍(如血脂异常和糖尿病肾病)相关的II型糖尿病动物模型。此外,糖尿病性血脂异常也与血管和肾小球损害有关。限制饮食中的脂肪是当前解决肥胖的策略,替米沙坦作为一种肾脏保护剂,可以通过激活PPARγ介导胆固醇外流。为了检验两种治疗选择均可能影响ZDF大鼠血脂异常和肾病的假说,我们研究了它们对糖尿病发展的影响。方法雄性Zücker糖尿病肥胖(ZDF)大鼠接受低热量饮食,媒介物或替米沙坦治疗9周。获得血样用于分析脂质和脂蛋白,LDL-氧化性,HDL结构和功能特性。进行尿液分析以估计白蛋白损失。实验结束时,处死大鼠,提取肝脏并定量APOA1 mRNA。结果结果表明,低热量饮食和替米沙坦可以减慢明显的高血糖症发作和以蛋白尿为标准的肾损害。两种干预均降低了LDL和肝APOA1 mRNA表达的氧化敏感性,但仅饮食限制降低了高脂血症。结论替米沙坦的饮食或药物干预对肥胖相关的II型糖尿病的LDL氧化敏感性和蛋白尿进展具有重要的有益作用。

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