血红素加氧酶1诱导自噬减轻小鼠肝脏缺血再灌注损伤

Heme oxygenase 1 induced autophagy in the alleviation of liver ischemia reperfusion injury

  • 摘要:
    目的 探讨小鼠肝脏缺血再灌注(IR)后血红素加氧酶1(HO-1)表达与自噬的相关性以及对肝功能的影响。方法 建立对照组,IR组,HO-1诱导剂Hemin预处理后IR组(Hemin+IR组)及HO-1抑制剂Znpp预处理后IR组(Znpp+IR组按不同灌注时间,IR组分为0、2、6、12、24、48、72 h组,Hemin+IR组和Znpp+IR组分为0、2、6、12、24 h组。检测各组小鼠血清ALT、AST水平以评估肝功能;HE染色评估肝脏形态学改变,电镜检查观察肝脏组织内自噬小体情况;Western blot法检测HO-1及自噬相关蛋白LC3II的蛋白水平。多组间比较采用方差分析,两组比较采用t检验,两两之间比较采用SNK-q检验。结果 IR组、Hemin+IR组及Znpp+IR组小鼠各时间点血清ALT、AST值均高于对照组,组间比较,差异有统计学意义(F=96.17,85.53,P<0.05);IR组缺血再灌注后12、24 h的血清ALT、AST值均高于Hemin+IR组相应时间点的值,两者比较,差异有统计学意义(qALT=-14.46,-7.85;qAST=-12.98,-5.26,P<0.05);而低于Znpp+IR组相应时间点的值,两者比较,差异有统计学意义(qALT=4.25,4.94;qAST=4.98,3.53,P<0.05)。HE染色示肝脏IR损伤在Hemin+IR组较IR组和Znpp+IR组显著改善,应用Suzuki分级进行半定量分析,对照组、IR12 h组、Hemin+IR 12 h组、Znpp+IR12 h组肝脏IR损伤评分分别为:0.5±0.3、2.6±0.5、1.1±0.3、3.0±0.4,组间比较,差异有统计学意义(F=53.62,P<0.05)。IR12h组分别与Hemin+IR12h组和Znpp+IR12h组比较,差异有统计学意义(q=10.67,14.02,P<0.05)。电镜检查示:IR组小鼠肝脏自噬小体较对照组明显增加,在Hemin+IR组增加更明显,而Znpp+IR组较IR组有所减少,对照组、IR12h组、Hemin+IR12h组、Znpp+IR12h组每10个视野的自噬小体平均数量分别为:(0.4±0.2)个、(1.8±0.6)个、(4.0±1.8)个、(0.7±0.5)个,组间比较,差异有统计学意义(F=21.35,P<0.05);IR 12 h组分别与Hemin+IR 12 h组和Znpp+IR 12 h组比较,差异有统计学意义(q=6.05,-3.03,P<0.05)。HO-1及自噬相关蛋白LC3II的表达在IR组及Hemin+IR组显著增加,且Hemin+IR 6、12h组HO-1蛋白相对表达量分别为0.64±0.17、0.51±0.12;LC3II蛋白相对表达量分别为1.04±0.20、1.20±0.23,高于IR组相应时间点的蛋白相对表达量HO-1:0.45±0.08、0.17±0.03;LC3II:0.58±0.04、0.95±0.14,两组比较,差异有统计学意义(tHO-1=4.03,4.69;tLC3II=4.29,6.69,P<0.05);而Znpp+IR 6、12 h组HO-1蛋白相对表达量分别为0.23±0.03、0.14±0.02;LC3II蛋白相对表达量分别为0.35±0.04,0.49±0.14,低于IR组相应时间点的蛋白相对表达量,两组比较,差异有统计学意义(tHO-1=13.82,7.04;tLC3II=7.21,4.03,P<0.05)。结论HO-1的表达与肝功能改善呈正相关,且其可能是通过诱导体内自噬来实现的。
     

     

    Abstract:
    Objective To investigate the correlation of heme oxygenase1 (HO-1) expression and autophagy in mice with liver ischemia reperfusion (IR) injury, and to study the influence of HO-1 on the hepatic function. Methods Control group, IR group, Hemin+IR group and Znpp+IR group were constructed. Mice in the Hemin+IR group and the Znpp+IR group were pretreated by Hemin (HO-1 inducer) and Znpp (HO-1 inhibitor) before IR. According to different reperfusion time, the IR group was divided into the 0, 2, 6, 12, 24, 48 and72 hours groups, and the Hemin+IR group and the Znpp+IR group were divided into the 0, 2, 6, 12, 24 hours groups. The levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were detected to evaluate the hepatic function. The autophagosome and pathological changes of liver were observed under electron microscope and hematoxylin and eosin (HE) staining, respectively. The expressions of HO-1 and autophagy associated  protein (LC3II) in the protein level were detected by Western blot. All data were analyzed using the analysis of variance, t test and q test, respectively. Results The levels of ALT and AST of the IR group, Hemin+IR group and Znpp+IR group were significantly higher than those of the control group (F=96.17, 85.53, P<0.05). The levels of ALT and AST of the IR 12 hours group and 24 hours group were significantly higher than those of the Hemin+IR 12 hours group and 24 hours group (qALT=-14.46,-7.85; qAST=-12.98,-5.26, P<0.05), but significantly lower than those of the Znpp+IR 12 hours group and 24 hours group (qALT=4.25, 4.94; qAST=4.98, 3.53, P<0.05). The results of HE staining showed that hepatic IR injury was significalty alleviated in the Hemin+IR group when compared with the IR group and the Znpp+IR group. The Suzuki degrees of hepatic IR injury in the control group, IR 12 hours group, Hemin+IR 12 hours group and the Znpp+IR 12 hours group were 0.5±0.3, 2.6±0.5, 1.1±0.3, 3.0±0.4, respectively, with significant differences among the 4 groups (F=53.62, P<0.05). There were significant difference in the Suzuki degrees of hepatic IR injury between the IR 12 hours group and the Hemin+IR 12 hours group, and between the IR 12 hours group and the Znpp+IR 12 hours group (q=10.67,14.02, P<0.05). The results of electron microscopy showed that the number of auto phagosome in the IR group was greater than the control group and Znpp+IR group, but lesser than the Hemin+IR group. The numbers of autophagosome in every 10 high power fields of the control group, IR 12 hours group, Hemin+IR12 hours group and the Znpp+IR 12 hours group were 0.4±0.2, 1.8±0.6, 4.0±1.8, 0.7±0.5, respectively, with significant difference among the 4 groups (F=21.35, P<0.05). There were significant differences in the number of autophagosome between the IR 12 hours group and the Hemin+IR 12 hours group, and between the IR 12 hours group and the Znpp+IR 12 hours group (q=6.05,-3.03, P<0.05). The expressions of HO-1 and LC3II in the IR group and the Hemin+IR group were significantly increased. The relative expressions of HO-1 protein in the Hemin+IR 6 hours group and the 12 hours group were 0.64±0.17 and 0.51±0.12,which were significantly higher than 0.45±0.08 and 0.17±0.03 of the IR 6 hours group and 12 hours group (t=4.03, 4.69, P<0.05).The relative expressions of LC3II protein in the Hemin+IR 6 hours group and the 12 hours group were 1.04±0.20 and 1.20±0.23, which were significantly higher than 0.58±0.04 and 0.95±0.14 of the IR 6 hours group and 12 hours group (t=4.29, 6.69, P<0.05). The relative expressions of HO-1 protein in the Znpp+IR 6 hours group and 12 hours group were 0.23±0.03, 0.14±0.02, respectively, and the relative expressions of LC3II protein were 0.35±0.04 and 0.49±0.14, which were significantly lower than the HO-1 and LC3II protein expressions in the IR 6 hours group and 12 hours group (tHO-1=13.82, 7.04; tLC3II=7.21, 4.03, P<0.05). Conclusion HO-1 is positively related to the amelioration of hepatic function, and it may be achieved by induction of autophagy.

     

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