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

Author:

Fu Feng12,Tian Fei2,Zhou Heping3,Lv Weifeng2,Tie Ru2,Ji Lele12,Li Rong4,Shi Zhenwei2,Yu Liming2,Liang Xiangyan2,Xing Wenjuan1,Xing Jinliang2,Yu Jun2,Sun Lijun4,Zhu Hailong3,Zhang Haifeng2

Affiliation:

1. Department of Physiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China

2. Experiment Teaching Center, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China

3. Department of Cardiac Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China

4. Department of Geratology and Department of Radiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China

Abstract

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.

Publisher

World Scientific Pub Co Pte Lt

Subject

Complementary and alternative medicine,General Medicine

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