Suppression of Excessive Histone Deacetylases Activity in Diabetic Hearts Attenuates Myocardial Ischemia/Reperfusion Injury via Mitochondria Apoptosis Pathway

被引:32
作者
Wu, Yang [1 ]
Leng, Yan [1 ]
Meng, Qingtao [1 ]
Xue, Rui [1 ]
Zhao, Bo [1 ]
Zhan, Liying [1 ]
Xia, Zhongyuan [1 ]
机构
[1] Wuhan Univ, Dept Anesthesiol, Renmin Hosp, Wuhan 430060, Hubei Province, Peoples R China
基金
中国国家自然科学基金;
关键词
OXIDATIVE STRESS; CELL-DEATH; CLASS-I; SODIUM-BUTYRATE; HDAC INHIBITORS; ACETYLATION; EXPRESSION; PROTECTION; BIM; REPERFUSION;
D O I
10.1155/2017/8208065
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Histone deacetylases (HDACs) play a pivotal role in signaling modification and gene transcriptional regulation that are essential for cardiovascular pathophysiology. Diabetic hearts with higher HDACs activity were more vulnerable to myocardial ischemia/reperfusion (MI/R) injury compared with nondiabetic hearts. We are curious about whether suppression of excessive HDACs activity in diabetic heart protects against MI/R injury. Methods. Diabetic rats were subjected to 45 min of ischemia, followed by 3 h of reperfusion. H9C2 cardiomyocytes were exposed to high glucose for 24 h, followed by 4 h of hypoxia and 2 h of reoxygenation (H/R). Results. Both MI/R injury and diabetes mellitus elevated myocardium HDACs activity. MI/R induced apoptotic cell death was significantly decreased in diabetic rats treated with HDACs inhibitor trichostatin A (TSA). TSA administration markedly moderated dissipation of mitochondrial membrane potential, protected the integrity of mitochondrial permeability transition pore (mPTP), and decreased cell apoptosis. Notably, cotreatment with Akt inhibitor partly or absolutely inhibited the protective effect of TSA in vivo and in vitro. Furthermore, TSA administration activated Akt/Foxo3a pathway, leading to Foxo3a cytoplasm translocation and attenuation proapoptosis protein Bim expression. Conclusions. Both diabetes mellitus and MI/R injury increased cardiac HDACs activity. Suppression of HDACs activity triggered protective effects against MI/R and H/R injury under hyperglycemia conditions through Akt-modulated mitochondrial apoptotic pathways via Foxo3a/Bim.
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页数:15
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