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Hydrogen sulfide ameliorates ischemia/reperfusion-induced hepatitis by inhibiting apoptosis and autophagy pathways.

Ping Cheng | Fan Wang | Kan Chen | Miao Shen | Weiqi Dai | Ling Xu | Yan Zhang | Chengfen Wang | Jingjing Li | Jing Yang | Rong Zhu | Huawei Zhang | Yuanyuan Zheng | Jie Lu | Yingqun Zhou | Chuanyong Guo
Mediators of inflammation | 2014

Hepatic ischemia/reperfusion (I/R) injury is an important clinical problem, and its consequences can seriously threaten human health. Apoptosis and autophagy have been shown to contribute to cell death in hepatic I/R injury. Hydrogen sulfide (H2S) is the third most common endogenously produced gaseous signaling molecule and is known to exert a protective effect against hepatic I/R injury. In this study, the purpose is to explore both the effect and mechanism of H2S on hepatic I/R injury.

Pubmed ID: 24966472

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BALB/cAnNCrl (tool)

RRID:MGI:2683685

laboratory mouse with name BALB/cAnNCrl from MGI.

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