中华临床医师杂志(电子版)
中華臨床醫師雜誌(電子版)
중화림상의사잡지(전자판)
CHINESE JOURNAL OF CLINICIANS(ELECTRONIC VERSION)
2014年
12期
2307-2310
,共4页
饶艳%邓少剑%何志恩%柯剑娟%王焱林%陈永权
饒豔%鄧少劍%何誌恩%柯劍娟%王焱林%陳永權
요염%산소검%하지은%가검연%왕염림%진영권
肝%再灌注损伤%补体膜攻击复合物
肝%再灌註損傷%補體膜攻擊複閤物
간%재관주손상%보체막공격복합물
Liver%Reperfusion injury%Complement membrane attack complex
目的:探讨膜攻击复合物C5b-9在大鼠肝脏缺血再灌注损伤中的表达。方法健康雄性SD大鼠60只,180~200 g,随机分为5组(n=12):假手术组(S组)、全肝再灌组1 h组(I/R 1 h组)、3 h组(I/R 3 h组)、6 h组(I/R 6 h组)和24 h组(I/R 24 h组)。制备大鼠全肝缺血再灌注模型,再灌注1、3、6、24 h末,取血测定谷丙转氨酶(ALT)和总胆红素(TBIL)浓度。取肝脏组织,检测C5b-9 mRNA和C5b-9蛋白的表达。结果与对照组比较,I/R各组大鼠ALT和TBIL水平均明显升高,I/R 3 h组达到高峰(P<0.05);I/R各组C5b-9的mRNA表达和C5b-9蛋白含量均有显著升高,且随着缺血再灌注时间的延长而逐渐升高,其中I/R 24 h组最高(P<0.05)。结论补体C5b-9参与肝缺血再灌注的损伤,尤其是在再灌注24 h时达到高峰。
目的:探討膜攻擊複閤物C5b-9在大鼠肝髒缺血再灌註損傷中的錶達。方法健康雄性SD大鼠60隻,180~200 g,隨機分為5組(n=12):假手術組(S組)、全肝再灌組1 h組(I/R 1 h組)、3 h組(I/R 3 h組)、6 h組(I/R 6 h組)和24 h組(I/R 24 h組)。製備大鼠全肝缺血再灌註模型,再灌註1、3、6、24 h末,取血測定穀丙轉氨酶(ALT)和總膽紅素(TBIL)濃度。取肝髒組織,檢測C5b-9 mRNA和C5b-9蛋白的錶達。結果與對照組比較,I/R各組大鼠ALT和TBIL水平均明顯升高,I/R 3 h組達到高峰(P<0.05);I/R各組C5b-9的mRNA錶達和C5b-9蛋白含量均有顯著升高,且隨著缺血再灌註時間的延長而逐漸升高,其中I/R 24 h組最高(P<0.05)。結論補體C5b-9參與肝缺血再灌註的損傷,尤其是在再灌註24 h時達到高峰。
목적:탐토막공격복합물C5b-9재대서간장결혈재관주손상중적표체。방법건강웅성SD대서60지,180~200 g,수궤분위5조(n=12):가수술조(S조)、전간재관조1 h조(I/R 1 h조)、3 h조(I/R 3 h조)、6 h조(I/R 6 h조)화24 h조(I/R 24 h조)。제비대서전간결혈재관주모형,재관주1、3、6、24 h말,취혈측정곡병전안매(ALT)화총담홍소(TBIL)농도。취간장조직,검측C5b-9 mRNA화C5b-9단백적표체。결과여대조조비교,I/R각조대서ALT화TBIL수평균명현승고,I/R 3 h조체도고봉(P<0.05);I/R각조C5b-9적mRNA표체화C5b-9단백함량균유현저승고,차수착결혈재관주시간적연장이축점승고,기중I/R 24 h조최고(P<0.05)。결론보체C5b-9삼여간결혈재관주적손상,우기시재재관주24 h시체도고봉。
ObjectiveTo investigate the expression of the membrane attack complex C5b-9 on total hepatic ischemia-reperfusion injury in rats.MethodsSixty male healthy SD rats weighing 180-200 g were randomly divided into 5 groups: control group (S group) and 1 h, 3 h, 6 h and 24 h hepatic ischemia-reperfusion group(I/R 1 h, 3 h, 6 h and 24 h,n=12). The hepatic I/R model was reproduced, and the concentration of alanine aminotransferase (ALT) and total bilirubin (TBIL) in blood was determined respectively in end of reperfusion for 1, 3, 6, 24 h; Hepatic tissues were obtained and the expression of C5b-9 gene and C5b-9 protein involved in all groups were detected.ResultsCompared with control group, the concentration of ALT and TBIL was increased significantly in all I/R groups (P<0.05), which was increased to the peak in I/R 3 h group. The expression of C5b-9 mRNA and protein detected in all I/R groups were higher than those of the control group (P<0.05) and were peaked in I/R 24 h group. ConclusionActivation of C5b-9 was one of the mechanisms in hepatic ischemia reperfusion injury, especially in the reperfusion for 24 hours.