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Melatonin Inhibits mTOR-Dependent Autophagy during Liver Ischemia/Reperfusion
Author(s) -
JungWoo Kang,
HongIk Cho,
SunMee Lee
Publication year - 2014
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000356647
Subject(s) - autophagy , pi3k/akt/mtor pathway , calpain , melatonin , reperfusion injury , endogeny , ischemia , microbiology and biotechnology , chemistry , phosphorylation , reactive oxygen species , pharmacology , biology , apoptosis , signal transduction , medicine , endocrinology , biochemistry , enzyme
Autophagy is a self-digestion system responsible for maintaining cellular homeostasis and interacts with reactive oxygen species produced during ischemia/reperfusion (I/R). Melatonin (MLT) is a potent and endogenous anti-oxidant that has beneficial effects in liver I/R injury. In this study, we examined the cytoprotective mechanisms of MLT in liver I/R, focusing on autophagic flux and associated signaling pathways.

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