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李波, 杨萌, 刘景伟, 胡春阳. HRS调控凋亡相关蛋白Bcl-xL、Bad、Bcl-2、Bax对大鼠心肌缺血再灌注损伤影响[J]. 中国公共卫生, 2015, 31(7): 889-892. DOI: 10.11847/zgggws2015-31-07-09
引用本文: 李波, 杨萌, 刘景伟, 胡春阳. HRS调控凋亡相关蛋白Bcl-xL、Bad、Bcl-2、Bax对大鼠心肌缺血再灌注损伤影响[J]. 中国公共卫生, 2015, 31(7): 889-892. DOI: 10.11847/zgggws2015-31-07-09
LI Bo, YANG Meng, LIU Jing-wei.et al, . Effects of HRS on apoptosis-related protein Bcl-xL,Bad,Bcl-2,and Bax and on myocardial ischemia-reperfusion injury in rats[J]. Chinese Journal of Public Health, 2015, 31(7): 889-892. DOI: 10.11847/zgggws2015-31-07-09
Citation: LI Bo, YANG Meng, LIU Jing-wei.et al, . Effects of HRS on apoptosis-related protein Bcl-xL,Bad,Bcl-2,and Bax and on myocardial ischemia-reperfusion injury in rats[J]. Chinese Journal of Public Health, 2015, 31(7): 889-892. DOI: 10.11847/zgggws2015-31-07-09

HRS调控凋亡相关蛋白Bcl-xL、Bad、Bcl-2、Bax对大鼠心肌缺血再灌注损伤影响

Effects of HRS on apoptosis-related protein Bcl-xL,Bad,Bcl-2,and Bax and on myocardial ischemia-reperfusion injury in rats

  • 摘要: 目的 探讨氢气饱和生理盐水(HRS) 调控凋亡相关蛋白Bcl-xL、Bad、Bcl-2、Bax对大鼠心肌缺血再灌注损伤的影响。方法 36只健康雄性SD大鼠随机分为假手术组、缺血再灌注损伤组和HRS处理组,每组12只;采用经典造模法建立心肌缺血再灌注损伤模型,3组制模成功后再灌注2 h,评价造模效果及Bcl-xL、Bad、Bcl-2、Bax等相关凋亡蛋白的表达。结果 大鼠心脏缺血再灌注损伤2 h后,假手术组、缺血再灌注损伤组、HRS处理组Bcl-xL mRNA和蛋白表达分别为(2.41±0.13)和(2.71±0.11)、(0.82±0.08)和(0.72±0.03)、(1.96±0.12)和(2.07±0.12),Bcl-2 mRNA和蛋白表达分别为(2.12±0.07)和(2.51±0.08)、(0.50±0.04)和(0.83±0.07)、(1.62±0.03)和(1.92±0.05),Bad mRNA和蛋白表达分别为(0.27±0.06)和(0.53±0.04)、(1.03±0.05)和(1.24±0.03)、(0.48±0.02)和(0.72±0.05),Bax mRNA和蛋白表达分别为(0.51±0.03)和(0.47±0.05)、(1.53±0.05)和(1.25±0.03)、(0.52±0.03)和(0.93±0.03);3组Bcl-xL、Bad、Bcl-2、Bax mRNA和蛋白表达分别比较,差异均有统计学意义(均P<0.05)。结论 HRS可通过调控Bcl-xL、Bad、Bcl-2、Bax凋亡相关蛋白的表达较为有效地减轻大鼠心肌缺血再损伤,进而保护心肌细胞。

     

    Abstract: Objective To study effects of hydrogen saturated saline(HRS) on expressions of apoptosis-related protein Bcl-xL,Bad,Bcl-2,and Bax and on myocardial ischemia-reperfusion injury in rats.Methods Thirty-six healthy male Sprague-Dawley(SD) rats were randomly divided into 3 groups(12 in each group):sham operation group(A),ischemia-reperfusion injury group(B),and HRS-treated group(C).Myocardial ischemia-reperfusion injury model was constructed using conventional method and a two hours reperfusion was performed after the establishment of the model among the rats of the 3 groups,and then the expressions of Bcl-xL,Bad,Bcl-2,and Bax were determeine.Results Compared to those of group C,left ventricular diastolic pressure(LVDP) and maximal first derivative of left ventricular diastolic pressure(LV Dp / dtmax) was significantly higher in group B.The observations with hematoxylin-eosin(HE) staining revealed cardiac cells arranged neatly in group A,obvious myocardial infarction in group B,and significantly reduced scope of infarction of cardiac cells in group C.The expressions of Bcl-xL and Bcl-2m RNA and protein were the highest in group A and the expressions in group C were significantly higher than those in group B(all P<0.05).Bad and Bax mRNA and protein expressions were the lowest in group A and the highest in group B,and the expressions in group C were significantly lower than those in group B(all P<0.05).Conclusion HRS can regulate apoptosis-related protein expressions of Bcl-xL,Bad,Bcl-2,and Bax and effectively reduce myocardial ischemia and reperfusion injury.

     

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