小鼠肝脏部分缺血再灌注损伤模型的建立

Establishment of mice model of partial hepatic ischemia reperfusion injury

  • 摘要: 目的 建立小鼠肝脏部分缺血再灌注损伤模型并分析损伤评估指标的变化趋势。
    方法 采用96只7~8周龄的纯系C57BL/6雄性小鼠作为研究对象,建立70%肝脏缺血再灌注损伤模型。按照缺血时间将小鼠分为假手术组和缺血30、60、90 min组,每组24只。各组小鼠分别于再灌注后6、12、24和48 h处死。通过检测血清ALT、AST、TNFα、IL6和巨噬细胞炎性蛋白2(MIP2)水平以及病理组织学评分、细胞凋亡指数等方法评估各组小鼠肝组织的损伤情况。两独立样本比较采用t检验。
    结果 术后88只小鼠存活,8只死亡,造模成功率为91.7%(88/96)。假手术组、缺血30、60、90 min组ALT水平分别为(35±24)U/L、(1703±442)U/L、(5133±681)U/L和(8233±808)U/L,缺血30、60、90 min组ALT水平显著高于假手术组(t=6.54,12.97,17.56,P<0.05);AST水平分别为(87±28)U/L、(2667±451)U/L、(6333±778)U/L和(9967±1168)U/L,缺血30、60、90 min组AST水平显著高于假手术组(t=9.89,13.89,14.65,P<0.05);TNFα水平分别为(14±5)μg/L、(83±14)μg/L、(133±17)μg/L和(202±21)μg/L,缺血30、60、90 min组TNFα水平显著高于假手术组(t=7.78,11.82,15.34,P<0.05);IL6水平分别为(32±9)μg/L、(493±168)μg/L、(844±166)μg/L和(1345±198)μg/L,缺血30、60、90min组IL6水平显著高于假手术组(t=4.74,8.46,11.48,P<0.05);MIP2水平分别为(37±11)μg/L、(102±35)μg/L、(177±32)μg/L和(279±50)μg/L,缺血30、60、90 min组MIP2水平显著高于假手术组(t=3.05,7.28,8.19,P<0.05);细胞凋亡指数分别为1.7%±2.1%、22.7%±8.6%、54.3%±11.2%和76.3%±14.8%,缺血30、60、90 min组细胞凋亡指数显著高于假手术组(t=4.10,8.04,8.63,P<0.05)。在缺血时间相同的情况下,随着再灌注时间的延长,各监测指标呈“抛物线”样变化趋势。
    结论 小鼠肝脏部分缺血再灌注损伤模型能较好地反映小鼠肝组织的损伤情况。随着缺血时间的延长,小鼠肝脏的缺血再灌注损伤程度逐渐加重;随着再灌注时间的延长,ALT、AST、TNFα、IL6、MIP2以及病理组织学评分和细胞凋亡指数均呈现“抛物线”样变化趋势。

     

    Abstract: Objective To establish mice model of partial hepatic ischemia reperfusion (IR) injury and investigate the variation trend of injury evaluation indexes.
    Methods Ninetysix male C57BL/6 mice (aged 7-8 weeks) were divided into 4 groups according to the ischemia time to construct hepatic IR model: sham operation group (24 mice), IR 30 minutes group (24 mice), IR 60 minutes group (24 mice) and IR 90 minutes group (24 mice). The mice in each group were sacrificed at hour 6, 12, 24, 48 after IR. The injury of the hepatic tissues in the 4 groups was analyzed based on detecting the levels of alanine transaminase (ALT), aspartate transaminase (AST), tumor necrosis factorα (TNFα), interleukin 6 (IL6), macrophage inflammatory protein 2 (MIP2), the histopathological grading and apoptosis index. All data were analyzed using the t test.
    Results Eight mice died, and the success rate of model construction was 91.7%(88/96). The levels of ALT in the sham operation group, IR 30, 60 and 90 minutes groups were (35±24)U/L, (1703±442)U/L, (5133±681)U/L and (8233±808)U/L, respectively. The levels of ALT in the IR 30, 60 and 90 minutes groups were significantly higher than the sham operation group (t=6.54, 12.97, 17.56, P<0.05). The levels of AST in the sham operation group, IR 30, 60 and 90 minutes groups were (87±28)U/L, (2667±451)U/L, (6333±778)U/L, (9967±1168)U/L, respectively. The levels of AST in the IR 30, 60 and 90 minutes groups were significantly higher than the sham operation group (t=9.89, 13.89, 14.65, P<0.05). The levels of TNFα in the sham operation group, IR 30, 60 and 90 minutes groups were (14±5)μg/L,(83±14)μg/L, (133±17)μg/L, (202±21)μg/L,respectively. The levels of TNFα in the IR 30, 60 and 90 minutes groups were significantly higher than the sham operation group (t=7.78, 11.82, 15.34, P<0.05). The levels of IL6 in the sham operation group, IR 30, 60 and 90 minutes groups were (32±9)μg/L, (493±168)μg/L, (844±166)μg/L, (1345±198)μg/L, respectively. The levels of IL6 in the IR 30, 60 and 90 minutes groups were significantly higher than the sham operation group (t=4.74, 8.46, 11.48, P<0.05). The levels of MIP2 in the sham operation group, IR 30, 60 and 90 minutes groups were (37±11)μg/L, (102±35)μg/L, (177±32)μg/L, (279±50)μg/L, respectively. The levels of MIP2 in the IR 30, 60 and 90 minutes groups were significantly higher than the sham operation group (t=3.05, 7.28, 8.19, P<0.05). The apoptotic indexes in the sham operation group, IR 30, 60 and 90 minutes groups were 1.7%±2.1%, 22.7%±8.6%, 54.3%±11.2% and 76.3%±14.8%, respectively. The levels of apoptotic indexes in the IR 30, 60 and 90 minutes groups were significantly higher than the sham operation group (t=4.10, 8.04, 8.63, P<0.05). Under the same ischemia time, the changes of ALT, AST, TNFα, IL6 and apoptosis index were presented as the parabolic style as the increase of the reperfusion time.
    Conclusions The mice model of hepatic IR injury could reflect the injured condition of the hepatic tissue of mice. Along with the time extension of ischemia, the severity of hepatic IR aggravated gradually. With the time extension of reperfusion, the levels of ALT, AST, TNFα, IL6, MIP2, histopathological grading and apoptosis index change in a parabolic trend.

     

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