Yi Xue, Cui Xiangyu, Wu Pengyu, Wang Shuai, Wang Gengye, Yang Xuehui, Yang Fang, Zheng Suqin, Li Zhanqing
Department of Pathology, Basic Medicine School of Hebei United University, Tangshan Hebei 063000, PR China.
Department of Cardiothoracic Surgery, Affiliated Hospital of Hebei United University, PR China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 Oct;27(10):1234-9.
To investigate the effect of N-acetylcysteine (NAC) on the apoptosis during myocardial ischemia reperfusion injury in rats' heart transplantation, and to explore the possible role of NAC in myocardial apoptosis.
Sixty healthy male Lewis rats (weighing, 200-220 g) were randomly divided into 3 groups, 20 rats each group (10 donors and 10 recipients). In control group, 1 mL normal saline was infused via inferior vena cava at 30 minutes before donor harvesting; in donor preconditioning group, NAC (300 mg/kg) was infused via inferior vena cava at 30 minutes before donor harvesting, but no treatment in recipients; and in recipient preconditioning group, NAC (300 mg/kg) was infused via inferior vena cava at 30 minutes before recipient transplantation, but no treatment in donors. Heart transplantation was established in each group. Blood was drawn at 6 and 24 hours after reperfusion for analysis of aspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH) as markers of graft injury; myocardial tissue was harvested to determine the superoxide dismutase (SOD) and lipid hydroperoxide (LPO) activity at 24 hours after reperfusion and to observe the histology and ultrastructural changes. Graft active Caspase-3 protein expression was measured by immunohistochemistry staining, and apoptosis index (AI) was calculated by TUNEL.
The heart transplantation operation was successfully completed in all groups, and the rats survived to the end of the experiment. The serum levels of AST, ALT, and LDH in donor and recipient preconditioning groups were significantly lower than those in control group at 6 hours after reperfusion (P < 0.05); the levels of AST and ALT in donor preconditioning group and the levels of AST and LDH in recipient preconditioning group were significantly lower than those in control group at 24 hours (P < 0.05); and no significant difference was found between donor and recipient perconditioning groups (P > 0.05). The levels of AST, ALT, and LDH at 24 hours were significantly lower than those at 6 hours in each group (P < 0.05) except the level of ALT in recipient preconditioning group (P > 0.05). SOD activity and SOD/LPO in donor and recipient preconditioning groups were significantly higher than those in control group (P < 0.05), but no significant difference between donor and recipient preconditioning groups (P > 0.05); there was no significant difference in LPO activity among 3 groups (P > 0.05). Histological staining and transmission electron microscope showed that myocardial injury in recipient preconditioning group was obviously lighter than that in donor preconditioning group and control group. Active Caspase-3 in recipient pretreatment group was significantly higher than that in donor preconditioning group and control group (P < 0.05). AI of donor and recipient preconditioning groups was significantly lower than that of control group (P < 0.05), but no significant difference was found between donor and recipient preconditioning groups (P > 0.05).
NAC can relieve ischemia reperfusion injury in rats' heart transplantation by improving myocardial SOD content, and reducing active Caspase-3 activity and AI, which has a protective effect on myocardial cell of donor heart.
探讨N-乙酰半胱氨酸(NAC)对大鼠心脏移植心肌缺血再灌注损伤过程中细胞凋亡的影响,以及NAC在心肌细胞凋亡中的可能作用。
将60只健康雄性Lewis大鼠(体重200-220 g)随机分为3组,每组20只(供体10只,受体10只)。对照组在供体心脏摘取前30分钟经下腔静脉输注1 mL生理盐水;供体预处理组在供体心脏摘取前30分钟经下腔静脉输注NAC(300 mg/kg),受体不做处理;受体预处理组在受体心脏移植前30分钟经下腔静脉输注NAC(300 mg/kg),供体不做处理。每组均进行心脏移植。再灌注6小时和24小时后采血,分析天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、乳酸脱氢酶(LDH)水平,作为移植损伤的标志物;再灌注24小时后取心肌组织,测定超氧化物歧化酶(SOD)和脂质过氧化产物(LPO)活性,并观察组织学和超微结构变化。采用免疫组化染色法检测移植心脏活性Caspase-3蛋白表达,TUNEL法计算凋亡指数(AI)。
所有组心脏移植手术均成功完成,大鼠存活至实验结束。再灌注6小时时,供体和受体预处理组血清AST、ALT和LDH水平均显著低于对照组(P<0.05);再灌注24小时时,供体预处理组AST和ALT水平、受体预处理组AST和LDH水平均显著低于对照组(P<0.05);供体和受体预处理组之间无显著差异(P>0.05)。除受体预处理组ALT水平外(P>0.05),每组24小时时AST、ALT和LDH水平均显著低于6小时时(P<0.05)。供体和受体预处理组SOD活性及SOD/LPO显著高于对照组(P<0.05),但供体和受体预处理组之间无显著差异(P>0.05);3组间LPO活性无显著差异(P>0.05)。组织学染色和透射电镜显示,受体预处理组心肌损伤明显轻于供体预处理组和对照组。受体预处理组活性Caspase-3显著高于供体预处理组和对照组(P<0.05)。供体和受体预处理组AI均显著低于对照组(P<0.05),但供体和受体预处理组之间无显著差异(P>0.05)。
NAC可通过提高心肌SOD含量、降低活性Caspase-3活性和AI减轻大鼠心脏移植缺血再灌注损伤,对供体心脏心肌细胞具有保护作用。