Quercetin attenuates renal ischemia/reperfusion injury via an activation of AMP-activated protein kinase-regulated autophagy pathway

被引:74
|
作者
Chen, Bo-Lin [1 ]
Wang, Li-Ting [1 ]
Huang, Kuo-How [2 ]
Wang, Ching-Chia [3 ]
Chiang, Chih-Kang [1 ,4 ]
Liu, Shing-Hwa [1 ,3 ,5 ]
机构
[1] Natl Taiwan Univ, Coll Med, Inst Toxicol, Taipei 10764, Taiwan
[2] Natl Taiwan Univ, Coll Med, Dept Urol, Taipei 10764, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Pediat, Taipei 10764, Taiwan
[4] Natl Taiwan Univ, Coll Med & Hosp, Dept Integrated Diagnost & Therapeut, Taipei 10764, Taiwan
[5] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
来源
JOURNAL OF NUTRITIONAL BIOCHEMISTRY | 2014年 / 25卷 / 11期
关键词
Quercetin; Renal ischemia/reperfusion injury; AMPK; Apoptosis; Autophagy; ISCHEMIA-REPERFUSION INJURY; INDUCED OXIDATIVE STRESS; SUPEROXIDE-DISMUTASE; PROXIMAL TUBULE; CELLS; KIDNEY; INHIBITION; APOPTOSIS; PHOSPHORYLATION; MTOR;
D O I
10.1016/j.jnutbio.2014.05.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Renal ischemia/reperfusion (I/R) is a major cause of acute renal failure. Quercetin, a flavonoid antioxidant, presents in many kinds of food. The molecular mechanism of quercetin on renal protection during I/R is still unclear. Here, we investigated the role of AMP-activated protein kinase (AMPK)-regulated autophagy in renal protection by quercetin. To investigate whether quercetin protects renal cells from I/R-induced cell injury, an in vitro model of I/R and an in vivo I/R model were used. Cell apoptosis was determined by propidium iodide/annexin V staining. Western blotting and immunofluorescence were used to determine the autophagy. AMPK expression was inhibited with appropriate short hairpin RNA (shRNA). In cultured renal tubular cell I/R model, quercetin decreased the cell injury, up-regulated the AMPK phosphorylation, down-regulated the mammalian target of rapamycin (mTOR) phosphorylation and activated autophagy during I/R. Knockdown of AMPK by shRNA transfection decreased the quercetin-induced autophagy but did not affect the mTOR phosphorylation. In I/R mouse model, quercetin decreased the increased serum creatinine level and altered renal histological score. Quercetin also increased AMPK phosphorylation, inhibited the mTOR phosphorylation and activated autophagy in the kidneys of I/R mice. These results suggest that quercetin activates an AMPK-regulated autophagy signaling pathway, which offers a protective effect in renal I/R injury. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1226 / 1234
页数:9
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