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Protective effect of ginsenoside Rb1 against myocardial ischemia/reperfusion injury in streptozotocin-induced diabetic rats

机译:人参皂苷Rb1对链脲佐菌素诱导的糖尿病大鼠心肌缺血/再灌注损伤的保护作用

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The objective of the current study is to investigate whether ginsenoside Rb1, a major pharmacological extract of ginseng that could attenuate myocardial ischemia reperfusion (MI/R) injury in non-diabetic myocardium, can attenuate MI/R injury in diabetes that are more vulnerable to ischemic insult. Rats were divided into seven groups: (i) diabetic sham, (ii) diabetic, (iii) normal, (iv) diabetic + ginsenoside Rb1, (v) diabetic + wortmannin, (vi) diabetic + wortmannin + ginsenoside Rb1, (vii) diabetic sham + wortmannin. Ginsenoside Rb1 and/or wortmannin were administered prior to inducing MI/R (30 min of coronary artery occlusion followed by 120 min reperfusion). At the end of the experiment, postischemic myocardial infarct size was significantly higher in the diabetic untreated group as compared to normal (P < 0.05), accompanied with increased myocardial apoptosis, elevated plasma CK-MB and LDH release and reduced blood pressure. Ginsenoside Rb1 reduced infarct size, cardiomyocyte apoptosis and caspase-3 activity compared to the diabetic group. The cardioprotective effects of ginsenoside Rb1 were cancelled by wortmannin. Ginsenoside Rb1 significantly upregulated phosphorylated Akt expression, which was attenuated by wortmannin. Ginsenoside Rb1 exerts cardioprotective effects against MI/R injury in diabetic rats, which is partly through activation of phosphatidylinositol 3-kinase (PI3 K)/Akt pathway. Thus this study shows a novel pharmacological preconditioning with ginsenoside Rb1 in the diabetic myocardium.
机译:本研究的目的是研究人参皂苷Rb1是人参的主要药理提取物,它可以减轻非糖尿病性心肌的心肌缺血再灌注(MI / R)损伤,是否可以减轻对糖尿病更易感的MI / R损伤缺血性侮辱。大鼠分为7组:(i)糖尿病假手术,(ii)糖尿病,(iii)正常,(iv)糖尿病+人参皂甙Rb1,(v)糖尿病+人参皂甙R,(vi)糖尿病+人参皂甙+人参皂甙Rb1,(vii )糖尿病假手术+渥曼青霉素。在诱导MI / R(冠状动脉闭塞30分钟,再灌注120分钟)之前,先服用人参皂甙Rb1和/或渥曼青霉素。在实验结束时,糖尿病未治疗组的缺血后心肌梗塞面积明显高于正常组(P <0.05),并伴有心肌细胞凋亡增加,血浆CK-MB和LDH释放升高以及血压降低。与糖尿病组相比,人参皂苷Rb1减少了梗塞面积,心肌细胞凋亡和caspase-3活性。人参皂甙Rb1的心脏保护作用被渥曼青霉素所抵消。人参皂苷Rb1显着上调了磷酸化的Akt表达,而渥曼青霉素则减弱了该表达。人参皂苷Rb1对糖尿病大鼠的MI / R损伤具有心脏保护作用,部分原因是通过激活磷脂酰肌醇3-激酶(PI3 K)/ Akt途径。因此,本研究显示了人参皂甙Rb1在糖尿病心肌中的新型药理预处理。

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