Ye Liang, Du Xinling, Xia Jiahong, Ping Jiang
Department of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
J Huazhong Univ Sci Technolog Med Sci. 2005;25(1):55-8. doi: 10.1007/BF02831387.
The mechanisms of rHu-EPO attenuating the apoptosis after myocardial infarction in rats were studied. Thirty-two rats were divided into three groups: sham operation group (Sham), acute myocardial infarction group (MI) and rHu-EPO-treated group (MI+ EPO). Acute myocardial infarction model was made by ligating the anterior descending coronary artery. rHu-EPO was administered i. p. in MI+EPO group at the dose of 5 000 IU/kg body weight immediately after the ligation. Each rat in MI+EPO group received the same dose of rHu-EPO daily the next 6 days. On the 14th day all rats underwent hemodynamic measurements and then killed. The samples were examined with HE stain, immunohistochemistry technique (bcl-2, bax) and TUNEL dyeing. The results showed that hemodynamic function in MI+ EPO group was much better than in MI group. The number of the cells positive for bax and TUNEL in MI+ EPO group was less than that in MI group. The number of the cells positive for bcl-2 in MI+ EPO group was more than that in MI group. These findings suggested that rHu-EPO could treat myocardial infarction by preventing apoptosis and attenuating post-infarction deterioration in hemodynamic function.
研究了重组人促红细胞生成素(rHu-EPO)减轻大鼠心肌梗死后细胞凋亡的机制。将32只大鼠分为三组:假手术组(Sham)、急性心肌梗死组(MI)和rHu-EPO治疗组(MI+EPO)。通过结扎冠状动脉前降支制备急性心肌梗死模型。MI+EPO组在结扎后立即腹腔注射rHu-EPO,剂量为5000IU/kg体重。MI+EPO组的每只大鼠在接下来的6天内每天接受相同剂量的rHu-EPO。在第14天,所有大鼠进行血流动力学测量,然后处死。样本进行苏木精-伊红(HE)染色、免疫组织化学技术(bcl-2、bax)和TUNEL染色检查。结果显示,MI+EPO组的血流动力学功能明显优于MI组。MI+EPO组中bax和TUNEL阳性细胞数少于MI组。MI+EPO组中bcl-2阳性细胞数多于MI组。这些结果表明,rHu-EPO可通过预防细胞凋亡和减轻梗死后血流动力学功能恶化来治疗心肌梗死。