Metformin ameliorates acetaminophen hepatotoxicity via Gadd45β-dependent regulation of JNK signaling in mice

被引:5
|
作者
Kim, Yong-Hoon [1 ]
Hwang, Jung Hwan [1 ]
Kim, Kyoung-Shim [1 ]
Noh, Jung-Ran [1 ]
Choi, Dong-Hee [1 ]
Kim, Don-Kyu [2 ]
Tadi, Surendar [3 ]
Yim, Yong-Hyeon
Choi, Hueng-Sik [2 ]
Lee, Chul-Ho [1 ]
机构
[1] Univ Sci & Technol, Korea Res Inst Biosci & Biotechnol, Lab Anim Resource Ctr, Daejeon 305806, South Korea
[2] Chonnam Natl Univ, Sch Biol Sci & Technol, Ctr Nucl Receptor Signals, Natl Creat Res Initiat, Gwangju, South Korea
[3] Korea Res Inst Stand & Sci, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
Acetaminophen; Hepatotoxicity; Gadd45; beta; JNK; Metformin; INDUCED HEPATIC-NECROSIS; INDUCED LIVER-INJURY; ACTIVATED PROTEIN-KINASE; KAPPA-B ACTIVATION; DRUG-METABOLISM; RECEPTOR CAR; FAILURE; REGENERATION; EXPRESSION; CELLS;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Acetaminophen (APAP) overdose is a leading cause of drug-induced acute liver failure. Prolonged c-Jun N-terminal kinase (JNK) activation plays a central role in APAP-induced liver injury and growth arrest, and DNA damage-inducible 45 beta (Gadd45 beta) is known to inhibit JNK phosphorylation. Metformin has recently been shown to have hepatoprotective effects. The aim of the present study is to investigate whether metformin mitigates APAP-induced hepatotoxicity and to ascertain the molecular basis of this effect. Methods: We used APAP- and/or metformin-treated Gadd45 beta knockout (KO) mice and wild type (WT) C57BL/6J control mice. Primary mouse hepatocytes were isolated from WT and Gadd45 beta KO mice were used for in vitro study. Results: Metformin pretreatment protected against APAP toxicity with decreased liver damage, and inhibited APAP-induced prolonged hepatic JNK phosphorylation in WT mice. Gadd45 beta expression was increased after APAP treatment, and the expression of Gadd45 beta was further enhanced by metformin. The effects of metformin on APAP-induced liver injury and JNK phosphorylation were abolished in Gadd45 beta KO mice. Notably, subtoxic doses of APAP caused cell death and sustained JNK phosphorylation in Gadd45 beta-deficient primary hepatocytes. In parallel, APAP increased mortality, severe liver injury, and JNK activation in Gadd45 beta KO mice. Interestingly, metformin administered after APAP treatment protected against APAP-evoked hepatotoxicity in WT mice, but not in Gadd45 beta KO mice. Conclusions: This study is the first to demonstrate that metformin shows protective and therapeutic effects against APAP overdose-evoked hepatotoxicity via Gadd45 beta-dependent JNK regulation. Metformin would be a promising therapeutic strategy for treatment of APAP overdose. (C) 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 82
页数:8
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