Agarwood Alcohol Extract Ameliorates Isoproterenol-Induced Myocardial Ischemia by Inhibiting Oxidation and Apoptosis

被引:15
|
作者
Wang, Canhong [1 ]
Peng, Deqian [2 ]
Liu, Yangyang [1 ]
Yu, Zhangxin [1 ]
Guo, Peng [1 ,3 ]
Wei, Jianhe [1 ,3 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, Hainan Prov Key Lab Resources Conservat & Dev Sou, Hainan Branch,Key Lab State Adm Traditional Chine, Haikou 570311, Hainan, Peoples R China
[2] Hainan Med Coll, Sch Pharm, Haikou 571199, Hainan, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, Key Lab Bioact Subst & Resources Utilizat Chinese, Natl Engn Lab Breeding Endangered Med Mat, Beijing 100193, Peoples R China
关键词
ISCHEMIA/REPERFUSION INJURY; RAT-HEART; REPERFUSION; ACTIVATION; EXPRESSION; IMMUNITY; INNATE;
D O I
10.1155/2020/3640815
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Agarwood is a traditional medicine used for treating some diseases, including painful and ischemic diseases. This study was carried out to investigate the potential cardioprotective effect of the whole-tree agarwood-inducing technique-produced agarwood alcohol extract (WTAAE) on isoproterenol- (ISO-) induced myocardial ischemia (MI) in rats and explore the underlying molecular mechanisms. Compared to the MI group, WTAAE pretreatment significantly improved ST wave abnormal-elevation, mitigated myocardial histological damage; decreased creatinine kinase (CK), lactate dehydrogenase (LDH), alanine transaminase (ALT), and aspartate transaminase (AST) levels; reduced hydrogen peroxide (H2O2) and lipid peroxide (LPO) production; and increased total antioxidant capacity (T-AOC) and catalase (CAT) activities. Moreover, agarwood alcohol extracts (AAEs) markedly enhanced the mRNA levels of Nrf2-ARE pathway, and Bcl-2 reduced the apoptotic Bax family mRNA expressions. In addition, the effect of WTAAE was greater than that of wild agarwood alcohol extract (WAAE) and burning-chisel-drilling agarwood alcohol extract (FBAAE). All of these data indicate that WTAAE exerted the protective effects of MI, and its mechanism was associated with upregulating Nrf2-ARE and suppressing Bcl-2 pathways.
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页数:10
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