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厄贝沙坦对大鼠血管平滑肌细胞Bcl-2/Bax蛋白表达及心肌细胞凋亡的影响
Study of Irbesartan on the Expression of Proteins Bcl-2/Bax in Small Intramycardial Arteries and on the Influence of Cardiomyocyte Apoptosis of Rats
【摘要】 目的 :观察自发性高血压大鼠 (SHR)心肌间小血管平滑肌细胞 (SMCs)Bcl 2和Bax蛋白的表达及心肌细胞凋亡指数(APOI) ;同时观察血管紧张素Ⅱ 1型受体 (AT1R)拮抗剂 厄贝沙坦对SHR心肌间小血管SMCsBcl 2和Bax蛋白表达及心肌细胞凋亡的影响。方法 :2 4只 16周龄SHR等分为厄贝沙坦 (30mg/kg/d ,2 0w)组和非厄贝沙坦组 ,另选 16周龄Wistar大鼠 (12只 )作为正常对照组。分别采用SP免疫组化法和末端脱氧核苷酸转移酶介导dUTP缺口末端标记法 (TUNEL)及病理检查方法检测Bcl 2和Bax蛋白水平的表达和APOI。结果 :非厄贝沙坦组与正常对照组比较 :收缩压明显增高 (P <0 0 1) ,左室重量指数 (LVW/BW)明显增加 (P <0 0 5 ) ;心肌间小血管SMCsBcl 2蛋白的表达明显增强 (P <0 0 5 ) ,心肌细胞APOI明显增加 (P<0 0 5 ) ,而Bax蛋白的表达两组无显著差别。厄贝沙坦组与非厄贝沙坦组比较 :收缩压明显降低 (P <0 0 1) ,LVW /BW明显下降 (P <0 0 5 ) ;SMCsBcl 2蛋白的表达及心肌细胞APOI明显减少 (P <0 .0 5 ) ,Bax蛋白的表达明显增强 (P <0 0 5 )。厄贝沙坦组与正常对照组比较 :Bax蛋白表达明显增强 (P <0 0 5 ) ,Bcl 2蛋白表达和APOI无明显差别。结论 :①SHR的小血管SMCs的凋亡受到抑制可能与Bcl 2蛋白的过度表达有关
【Abstract】 Objective: To investigate the expression of the proteins Bcl-2 and Bax in intramycardial arteries of SHR and Wistar rats,and the effects of angiotensinⅡ Type-1 receptor(AT 1R) antagonist-Irbesartan on the expression of proteins Bcl-2 and Bax and cardiomyocyte apoptosis in rats.Methods: Twenty-four rats were divided into Irbesartan group( n =12) and the group without Irbesartan( n =12) 12 rats as normal control group were chosen.The expression of the proteins Bcl-2 and Bax was determined by Immunhistochemia,cardiomyocyte apoptosis was identified by in situ TDT-mediated dUTP nick end labeling(TUNEL).Results:Compared with the normal control group,untreated SHR exhibited increased systolic blood pressure,left ventricular mass index,Bcl-2 expression,cardiomyocyte apoptosis inde (APOI) and similar Bax expression.Compared with the group without Irbesartan,systolic blood pressure was decreased,left ventricular mass index and Bcl-2 expression were significantly lower,APOI was reduced significantly in the Irbesartan group.Irbesartan group showed higher Bax expression than the group without Irbesartan and normal control group. Conclusion: The findings suggest that smooth muscle cell apoptosis may be inhibited in small arteries of adult SHR as a consequence of an excess of the protein Bcl-2.In addition,The results suggest that chronic AT 1R antagonist--Irbesartan restore the susceptibility to apoptosis in these cells through stimulation of the protein Bax.These results indicate that Irbesartan effectively inhibits cardiomyocyte apoptosis and reverses left ventricular hypertrophy.
【Key words】 Irbesartan; Left Ventricular Hypertrophy; Bcl-2/Bax Protein; Cell Apoptosis];
- 【文献出处】 汕头大学医学院学报 ,Journal of Shantou University Medical College , 编辑部邮箱 ,2002年04期
- 【分类号】R541.3
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