Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210093, China.
Evid Based Complement Alternat Med. 2012;2012:548430. doi: 10.1155/2012/548430. Epub 2012 May 29.
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.
高尿酸血症和血脂异常与 Cd 肾毒性有关。本研究旨在确定槲皮素(一种具有抗高尿酸血症和抗血脂异常特性的膳食类黄酮)对 3 和 6mg/kg Cd 暴露 4 周的大鼠肾脏 UA 转运系统改变和肾脏脂质蓄积紊乱的影响。Cd 暴露导致高尿酸血症,同时伴有肾脏 XOR 活性增强和 UA 排泄功能障碍。同时,在 Cd 暴露的大鼠中观察到肾脏 UA 转运相关蛋白(包括 RST、OAT1、MRP4 和 ABCG2)的异常表达水平,并且肾脏 Na(+)-K(+)-ATPase 的抑制活性。此外,Cd 暴露扰乱了脂质代谢,下调了 AMPK 及其下游靶标 PPARα、OCTN2 和 CPT1 的表达,上调了 PGC-1β 和 SREBP-1 的表达。我们已经证明,Cd 诱导的肾脏 UA 转运和产生系统紊乱可能与肾脏 AMPK-PPARα/PGC-1β信号通路损伤相互作用,导致大鼠 Cd 肾毒性。槲皮素被发现对 Cd 诱导的 RST 和 OAT1 表达失调具有治疗作用,同时抑制 XOR 活性和 AMPK-PPARα/PGC-1β 信号通路损伤,从而减少大鼠肾脏脂质蓄积。