Protective Effects of Tetrahydroxy Stilbene Glucoside on Diabetes Mellitus Combined with Myocardial Ischemia-Reperfusion Injury in Rats

被引:0
|
作者
Yi, Chun [1 ]
Yuan, Yueshuang [2 ]
Feng, Xiqiang [3 ]
机构
[1] Guangzhou Univ Chinese Med, Sch Nursing, Guangzhou 510006, Guangdong, Peoples R China
[2] Xinzao Hosp Panyu Dist Guangzhou City, Dept Nursing, Guangzhou 511436, Guangdong, Peoples R China
[3] Guangdong Women & Childrens Hosp, Pediat Intens Care Unit, Guangzhou 511400, Guangdong, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2019年 / 38卷 / 10期
关键词
apoptosis; diabetes mellitus; myocardial ischemia-reperfusion injury; oxidative stress; tetrahydroxy stilbene glucoside;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to investigate the effects of tetrahydroxy stilbene glucoside (TSG) on diabetes mellitus (DM) combined with myocardial ischemia-reperfusion injury (MIRI) in rats. Forty rats were randomly divided into 4 groups including control, TSG, DM+MIRI and DM+MIRI+TSG groups, 10 rats in each group. The rats in TSG and DM+MIRI+TSG were intragastrically administrated with 60 mg/kg TSG. The DM combined with MIRI model was established in DM+MIRI and DM+MIRI+TSG groups. The cardiac function, myocardial infarct, blood glucose, oxidative stress indexes and myocardial cell apoptosis-related protein expressions were determined. Results showed that, compared with DM+MIRI group, in DM+MIRI+TSG group the percentage of myocardial infarction area, fasting plasma glucose, hemoglobin A1, fasting insulin, serum lactate dehydrogenase, creatine kinase-MB, and myocardial malondialdehyde, B-cell lymphoma-2 associated X protein, and cysteinyl aspartate specific proteinase-3 protein levels were significantly decreased, and the left ventricular systolic pressure, +maximum left ventricular systolic/diastolic rate (dp/dt(max)) and -dp/dt(max), serum glutathione peroxidase, and myocardial superoxide dismutase and B-cell lymphoma-2 protein expression levels were significantly increased (all P < 0.05). In conclusion, TSG can alleviate DM combined with MIRI in rats by resisting oxidative stress and inhibiting myocardial cell apoptosis.
引用
收藏
页码:1915 / 1920
页数:6
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