Osthole attenuates myocardial ischemia/reperfusion injury in rats by inhibiting apoptosis and inflammation

被引:5
|
作者
Wu, Jingguo [1 ]
Yang, Yang [2 ]
Xun, Nan [3 ]
Zeng, Lijin [1 ]
Li, Zhenyu [1 ]
Yang, Wen [1 ]
Liang, Yanbing [1 ]
Ma, Zhongfu [1 ]
Tang, Hao [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Gen Internal Med, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Pathol, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Endocrinol, Guangzhou 510080, Guangdong, Peoples R China
来源
关键词
Osthole; myocardial ischemia; inflammatory; apoptosis; ISCHEMIA-REPERFUSION INJURY; CARDIAC INJURY; KAPPA-B; PATHWAY; MODEL; SUPPRESSION; EXPRESSION; PROTECTS; STRESS; CELLS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was performed to evaluate the cardioprotective effects of osthole (OST) in a rat model of myocardial ischemia/reperfusion injury (MI/RI) and the underlying mechanism. We exposed rat hearts to left anterior descending coronary artery ligation for 30 min followed by 24 h of reperfusion. The results showed that pretreatment with OST ameliorated MI/RI as evidenced by histopathological examination. Moreover, the terminal deoxynucleotidyl transferase dUTP nick end-labeling assay demonstrated that OST suppressed myocardial apoptosis, which may be related to an increase in the Bcl-2/Bax ratio and inhibition of caspase-3 and caspase-9 activation. Furthermore, we determined that OST ameliorated impaired mitochondrial morphology and the oxidation system; OST also attenuated levels of pro-inflammatory cytokines, including tumor necrosis factor alpha and interleukins 6 and 1 beta. In conclusion, OST exerted a strong favorable cardioprotective effect on MI/RI, possibly by suppressing the inflammatory response and inhibiting cell apoptosis.
引用
收藏
页码:1109 / 1116
页数:8
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