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槲皮素可预防镉诱导的大鼠肾脏尿酸转运系统改变和脂代谢紊乱。

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

机构信息

Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210093, China.

出版信息

Evid Based Complement Alternat Med. 2012;2012:548430. doi: 10.1155/2012/548430. Epub 2012 May 29.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/400f/3368504/304ce0e3469c/ECAM2012-548430.001.jpg

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