Sun Kai, Liu Zhi-su, Sun Quan
Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2009 Dec;29(12):2480-4.
To investigate the protective effect of ischemic postconditioning (IPC) against hepatic ischemia-reperfusion injury.
Twenty-four normal male Wistar rats were randomly divided into sham-operated group, ischemia-reperfusion group (IR) and IPC group, and in the latter two groups, the rats were subjected to acute hepatic ischemia-reperfusion. IPC was achieved by several brief pre-reperfusion and withdrawn before persistent reperfusion. The concentration of malondialdehyde (MDA) and activity of several antioxidant enzymes in the hepatic tissue were measured. The cell apoptosis was detected by TdT-mediated dUTP-biotin nick end labeling (TUNEL) and the expression of Bcl-2 protein measured by immunohistochemistry. The mitochondrial ultrastructural and morphological changes of the hepatic cells were observed by electron microscopy.
Compared with IR group, IPC group showed significantly reduced concentration of MDA and the hepatocellular apoptotic index (P<0.05) with markedly enhanced activity of the antioxidant enzymes and Bcl-2 protein expression (P<0.05).The mitochondrial ultrastructural damage was also relieved obviously in IPC group.
IPC can reduce the hepatocellular apoptosis after reperfusion and offers protection against hepatic IR injury.
探讨缺血后适应(IPC)对肝脏缺血再灌注损伤的保护作用。
将24只正常雄性Wistar大鼠随机分为假手术组、缺血再灌注组(IR)和IPC组,后两组大鼠均进行急性肝脏缺血再灌注。通过几次短暂的再灌注前处理实现IPC,并在持续再灌注前停止。检测肝组织中丙二醛(MDA)浓度和几种抗氧化酶的活性。采用TdT介导的dUTP生物素缺口末端标记法(TUNEL)检测细胞凋亡,免疫组织化学法检测Bcl-2蛋白表达。通过电子显微镜观察肝细胞的线粒体超微结构和形态变化。
与IR组相比,IPC组MDA浓度和肝细胞凋亡指数显著降低(P<0.05),抗氧化酶活性和Bcl-2蛋白表达明显增强(P<0.05)。IPC组线粒体超微结构损伤也明显减轻。
IPC可减少再灌注后肝细胞凋亡,对肝脏缺血再灌注损伤具有保护作用。