Semen Cassiae Attenuates Myocardial Ischemia and Reperfusion Injury in High-Fat Diet Streptozotocin-Induced Type 2 Diabetic Rats

被引:22
作者
Fu, Feng [1 ,2 ]
Tian, Fei [2 ]
Zhou, Heping [3 ]
Lv, Weifeng [2 ]
Tie, Ru [2 ]
Ji, Lele [1 ,2 ]
Li, Rong [4 ,5 ]
Shi, Zhenwei [2 ]
Yu, Liming [2 ]
Liang, Xiangyan [2 ]
Xing, Wenjuan [1 ]
Xing, Jinliang [2 ]
Yu, Jun [2 ]
Sun, Lijun [4 ,5 ]
Zhu, Hailong [3 ]
Zhang, Haifeng [2 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Physiol, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Xijing Hosp, Expt Teaching Ctr, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp, Dept Cardiac Surg, Xian 710032, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Geratol, Xian 710032, Peoples R China
[5] Fourth Mil Med Univ, Xijing Hosp, Dept Radiol, Xian 710032, Peoples R China
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2014年 / 42卷 / 01期
基金
中国国家自然科学基金;
关键词
Semen Cassiae; Myocardial Ischemia/Reperfusion; Diabetes; Apoptosis; Akt; ERK1/2; ISCHEMIA/REPERFUSION INJURY; SEED EXTRACT; OBTUSIFOLIA; TORA; ASSOCIATION; PATHWAYS; DISEASE; HEART; RISK;
D O I
10.1142/S0192415X14500062
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Obese patients with type 2 diabetes mellitus (T2DM), which is characterized by hyperglycemia, are liable to more severe myocardial infarction. Semen Cassiae is proven to reduce serum lipid levels. This study investigated whether the Semen Cassiae extract (SCE) reduces myocardial ischemia and reperfusion (MI/R) injury with or without diabetes and the underlying mechanisms. The high-fat diet-fed streptozotocin (HFD-STZ) rat model was created as a T2DM model. Normal and DM rats received SCE treatment orally (10 mg/kg/day) for one week. Subsequently these animals were subjected to MI/R. Compared with the normal animals, DM rats showed increased plasma total cholesterol (TC) and triacylglycerol (TG), and more severe MI/R injury and cardiac functional impairment. SCE treatment significantly reduced the plasma TC and TG, improved the instantaneous first derivation of left ventricle pressure and reduced infarct size, decreased plasma creatine kinase and lactate dehydrogenase levels, and apoptosis index at the end of reperfusion in diabetic rats. Moreover, SCE treatment increased the antiapoptotic protein Akt and ERK1/2 phosphorylation levels. Pretreatment with a PI3K inhibitor wortmannin or an ERK1/2 inhibitor PD98059 not only blocked Akt and ERK1/2 phosphorylation respectively, but also inhibited the cardioprotective effects of SCE. However, SCE treatment did not show any effects on the MI/R injury in the normal rats. Our data suggest that SCE effectively improves myocardial function and reduces MI/R-induced injury in diabetic but not normal animals, which is possibly attributed to the reduced TC/TG levels and the triggered cell survival signaling Akt and ERK1/2.
引用
收藏
页码:95 / 108
页数:14
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