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荷叶黄酮对大鼠心肌缺血再灌注损伤的保护作用 被引量:7

PROTECTIVE EFFECT OF NELUMBO FLAVONE ON MYOCARDIUM ISCHEMIA-REPERFUSION INJURY IN RAT
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摘要 目的 观察荷叶黄酮对大鼠心肌缺血再灌注损伤的保护作用,并探讨其可能的作用机制。方法 将4月龄雄性Wistar大鼠50只,随机分为对照组(10只)、模型组(20只)和治疗组(20只)。建立大鼠心肌缺血再灌注损伤模型,模型组和治疗组大鼠于冠状动脉结扎和再灌注前1min分别由左心腔缓慢注射生理盐水、荷叶黄酮(60mg/kg)。2h后处死动物,应用苏木精-伊红染色观察组织形态学的改变,应用免疫组织化学方法测定心肌组织中Bax蛋白、Bcl-2蛋白及Caspase-3的表达。结果 治疗组细胞水肿较模型组明显减轻。与模型组比较,治疗组Bax及Caspase-3蛋白的表达均明显降低,而Bcl-2蛋白的表达明显升高(F=3.33~4.17,q=3.34~8.03,P〈0.05)。结论 荷叶黄酮对大鼠心肌缺血再灌注损伤具有保护作用,其机制可能与上调Bcl-2、下调Bax和Caspase-3的表达,减少细胞凋亡有关。 Objective To investigate the protective effect of Nelumbo Flavone on myocardium ischemia-reperfusion injury in rat and probe into the mechanism of protection. Methods Fifty 4-month-old male SD rats were randomly divided into three groups: control group (10 rats), model group (20 rats), and treatment group (20 rats). A rat model of myocardium ischemiareperfusion injury was established. Rats in the model and treatment groups received intraventricular injection of normal saline and Nelumbo Flavone (60 mg/kg), respectively, one minute before coronary artery ligation and reperfusion. The animals were sacrificed two hours later. Eosin-hematoxylin (HE) staining was performed for morphology observation and immunohistochemistry staining was used to study the expressions of Bax, Bcl-2 and Caspase-3 proteins in myocardium. Results Compared with the model group, there was less myocardium edema in the treatment group. The expressions of Bax and Caspase-3 proteins were significantly lower and the expression of Bcl-2 was significantly higher in the treatment group (F= 3.33 - 4. 17; q = 3.34 - 8.03;P〈0.05). Conclusion Nelumbo Flavone shows protective effects on rat myocardium ischemia-reperfusion injury. The mechanism of protection might be related with up-regulation of Bcl-2, down-regulation of Bax, inhibition of Caspase-3 and reduction of cell apoptosis.
出处 《齐鲁医学杂志》 2009年第6期515-516,518,共3页 Medical Journal of Qilu
关键词 心肌 再灌注损伤 荷叶黄酮 BCL-2相关X蛋白质 基因 BCL-2 CASPASE-3 Myocardial Reperfusion injury Nelumbo flavone bcl-2-associated X protein Gene, bcl-2 Caspase-3
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