Xu Jun-mei, Tan Rong, Hu Dong-xu
Department of Anesthesiology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Hunan Yi Ke Da Xue Xue Bao. 2003 Apr;28(2):111-3.
To investigate the effects of ischemic preconditioning on myocardial bcl-2, bax, p53 gene expression during ischemia/reperfusion period in rabbits.
Twenty four rabbits were randomly allocated to three groups (n = 8), pseudo-operation group(Group P), ischemia/reperfusion group (Group IR) and ischemic preconditioning group(Group IP). Group IR and Group IP were subjected to three hours of left anterior descending coronary artery occlusion followed for three hours of reperfusion. Ischemic preconditioning was achieved by three 5-minute cycles of ischemia, each followed by 5 minutes of reperfusion. Apoptosis index(AI) and protein expression of Bcl-2, Bax, and p53 in the border zone of myocardium of ischemic area at risk were obtained with a flow cytometry.
Compared with Group IR, AI was significantly reduced in Group IP(P < 0.01). Bcl-2 expressions was higher in Group IP than in Group IR, while bax and p53 expressions were lower in Group IP than in Group IR.
The rabbit myocardial apoptosis induced by ischemic preconditioning inhibited ischemia-reperfusion in vivo partly related to the modulating of bcl-2, bax and p53 expression.
探讨缺血预处理对兔心肌缺血/再灌注期间bcl-2、bax、p53基因表达的影响。
将24只兔随机分为三组(n = 8),即假手术组(P组)、缺血/再灌注组(IR组)和缺血预处理组(IP组)。IR组和IP组均行左冠状动脉前降支阻断3小时,再灌注3小时。缺血预处理通过3个5分钟的缺血周期实现,每个缺血周期后再灌注5分钟。采用流式细胞术检测缺血危险区心肌边缘区的凋亡指数(AI)以及Bcl-2、Bax和p53的蛋白表达。
与IR组相比,IP组AI显著降低(P < 0.01)。IP组Bcl-2表达高于IR组,而IP组Bax和p53表达低于IR组。
缺血预处理诱导的兔心肌细胞凋亡抑制体内缺血-再灌注,部分与bcl-2、bax和p53表达的调节有关。