Activation of TGR5 restores AQP2 expression via the HIF pathway in renal ischemia-reperfusion injury

Author:

Han Mengke1,Li Suchun1,Xie Haixia1,Liu Qiaojuan1,Wang Ani2,Hu Shan1,Zhao Xiaoduo1,Kong Yonglun1,Wang Weidong134ORCID,Li Chunling1

Affiliation:

1. Institute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China

2. Cardiovascular Center, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China

3. Department of Pathophysiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China

4. Department of Nephrology, the Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China

Abstract

Stimulation of the membrane G protein-coupled bile acid receptor TGR5 by lithocholic acid (LCA) reduced polyuria in rats with renal ischemia-reperfusion (I/R) injury. LCA increased abundance of aquaporin-2 (AQP2) protein and upregulated hypoxia-inducible factor (HIF)-1α protein expression in association with decreased NF-κB p65 and IL-1β. After I/R, mice with tgr5 gene deficiency exhibited more severe decreases in AQP2 and HIF-1α protein abundance and inflammatory responses. TGR5 activation exhibits a protective role in acute renal injury induced by I/R.

Funder

National Natural Science Foundation of China

Publisher

American Physiological Society

Subject

Physiology

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