Open AccessMetformin attenuates myocardial ischemia-reperfusion injury via up-regulation of antioxidant enzymes
Author(s) -
Xiaoling Wang,
Lei Yang,
Licheng Kang,
Jing Li,
Liang Yang,
Jincai Zhang,
Jie Liu,
Mengmeng Zhu,
Qiong Zhang,
Yanna Shen,
Zhi Qi
Publication year - 2017
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0182777
Subject(s) - antioxidant , ampk , tunel assay , pharmacology , reperfusion injury , apoptosis , catalase , ex vivo , reactive oxygen species , metformin , chemistry , in vivo , ischemia , enzyme , medicine , in vitro , biochemistry , protein kinase a , endocrinology , biology , diabetes mellitus , microbiology and biotechnology
The objective was to examine the protective effect of metformin (Met) on myocardial ischemia-reperfusion (IR) injury and whether the mechanism was related to the AMPK/ antioxidant enzymes signaling pathway. Rat Langendorff test and H 2 O 2 -treated rat cardiomyocytes (H9c2) were used in this study. Met treatment significantly improved left ventricular (LV) function, reduced infarct size and CK-MB release in comparison with IR group. Decreased TUNEL staining positive cells were also observed in IR+Met group ex vivo . Met treatment markedly inhibited IR inducing cell death and significantly decreased apoptosis with few generations of reactive oxygen species (ROS) in H9c2 cells in comparison with IR group. Up-regulated expressions of phosphorylated LKB1/AMPK/ACC, as well as down-regulated expressions of apoptotic proteins (Bax and cleaved caspase 3) were found in IR+Met group when compared to the IR group. Importantly, Met significantly up-regulated the expression of antioxidant enzymes (MnSOD and catalase) during IR procedure either ex vivo or in vitro . Compound C, a conventional inhibitor of AMPK, abolished the promoting effect of Met on antioxidant enzymes, and then attenuated the protective effect of Met on IR injury in vitro . In conclusion, Met exerted protective effect on myocardial IR injury, and this effect was AMPK/ antioxidant enzymes dependent.