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Quercetin Protects against Cadmium-Induced Renal Uric Acid Transport System Alteration and Lipid Metabolism Disorder in Rats

机译:槲皮素可防止镉诱导的大鼠肾脏尿酸转运系统改变和脂质代谢紊乱

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摘要

Hyperuricemia and dyslipidemia are involved in Cd nephrotoxicity. The aim of this study was to determine the effect of quercetin, a dietary flavonoid with anti-hyperuricemic and anti-dyslipidemic properties, on the alteration of renal UA transport system and disorder of renal lipid accumulation in 3 and 6 mg/kg Cd-exposed rats for 4 weeks. Cd exposure induced hyperuricemia with renal XOR hyperactivity and UA excretion dysfunction in rats. Simultaneously, abnormal expression levels of renal UA transport-related proteins including RST, OAT1, MRP4 and ABCG2 were observed in Cd-exposed rats with inhibitory activity of renal Na+-K+-ATPase. Furthermore, Cd exposure disturbed lipid metabolism with down-regulation of AMPK and its downstream targets PPARα, OCTN2 and CPT1 expressions, and up-regulation of PGC-1β and SREBP-1 expressions in renal cortex of rats. We had proved that Cd-induced disorder of renal UA transport and production system might have cross-talking with renal AMPK-PPARα/PGC-1β signal pathway impairment, contributing to Cd nephrotoxicity of rats. Quercetin was found to be effective against Cd-induced dysexpression of RST and OAT1 with XOR hyperactivity and impairment of AMPK-PPARα/PGC-1β signal pathway, resulting in renal lipid accumulation reduction of rats.
机译:高尿酸血症和血脂异常与镉的肾毒性有关。这项研究的目的是确定槲皮素(一种具有抗高尿酸血症和抗血脂异常特性的饮食类黄酮)对暴露于3和6μmg/ kg Cd的肾脏UA转运系统和肾脂质蓄积障碍的影响大鼠持续4周。镉暴露引起高尿酸血症,并伴有肾脏XOR亢进和UA排泄功能障碍。同时,在镉暴露的大鼠中,对肾Na + -K + -ATP酶。此外,Cd暴露通过下调AMPK及其下游靶标PPARα,OCTN2和CPT1的表达以及上调PGC-1β和SREBP-1在大鼠肾皮质的表达而干扰脂质代谢。我们已经证明,镉诱导的肾脏UA运输和生产系统紊乱可能与肾脏AMPK-PPARα/PGC-1β信号通路障碍发生相互影响,从而导致大鼠镉肾毒性。发现槲皮素可有效抑制Cd诱导的RST和OAT1表达异常,并具有XOR过度活跃和AMPK-PPARα/PGC-1β信号通路受损,导致大鼠肾脂质蓄积减少。

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