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大鼠肝脏缺血再灌注损伤早期载脂蛋白M的表达
引用本文:许贤林,叶启发,何小舟,张晓膺,罗光华,朱江,Ning Xu,巢志复,张懋祖,张毅. 大鼠肝脏缺血再灌注损伤早期载脂蛋白M的表达[J]. 中国普通外科杂志, 2005, 14(7): 7-504
作者姓名:许贤林  叶启发  何小舟  张晓膺  罗光华  朱江  Ning Xu  巢志复  张懋祖  张毅
作者单位:1. 华中科技大学同济医学院附属同济医院,器官移植研究所,湖北,武汉,430030;苏州大学医学院第三附属医院,江苏,常州,213003
2. 华中科技大学同济医学院附属同济医院,器官移植研究所,湖北,武汉,430030
3. 苏州大学医学院第三附属医院,江苏,常州,213003
4. 瑞典荣德大学医院,临床化学研究所,瑞典,荣德,S-221
5. 中南大学湘雅三医院,移植医学研究院,湖南,长沙,410013
摘    要:目的 探讨大鼠肝缺血再灌注损伤早期肝内载脂蛋白M mRNA(apoM mRNA)及血浆apoM的表达。方法 建立大鼠肝脏缺血再灌注损伤模型。健康雄性SD大鼠40只随机分成5组,每组8只:假手术组(对照组);IR1组(灌注0.5h);[R2组(灌注1.0h);IR3组(灌注2.0h);[R4组(灌注3.0h)。缺血再灌注组的缺血时间统一为1.0h。检测血浆谷丙转氨酶水平(ALT)、肝组织病理变化、血浆apoM蛋白及肝组织apoM mRNA。结果 血浆ALT的水平随着灌注时间的延长而升高,肝组织损伤随着灌注时间的延长而逐渐加重。肝组织apoM mRNA的表达则先有一过性下降(灌注0.5h组),此后随着灌注时间的延长其表达明显增强。血浆apoM蛋白有相同的变化趋势,但其表达在灌注2.0h才有上升。结论 在肝缺血再灌注损伤过程中,肝脏apoM mRNA的表达和血浆蛋白水平有迅速、明显的变化,提示apoM可能具有急性时相反应蛋白的特性。

关 键 词:肝疾病 再灌注损伤 疾病模型,动物 载脂蛋白M
文章编号:1005-6947(2005)07-0501-04
收稿时间:1900-01-01
修稿时间:2004-03-28

Early apolipoprotein M expression in ischemia -reperfusion injury of rats
XU Xian lin,YE Qi f,HE Xiao zhou,ZHANG Xiao ying,LUO Guang hu,ZHU Jiang,Ning Xu,CAO Zhi fu,ZHANG Mao zu,ZHANG Yi . Early apolipoprotein M expression in ischemia -reperfusion injury of rats[J]. Chinese Journal of General Surgery, 2005, 14(7): 7-504
Authors:XU Xian lin  YE Qi f  HE Xiao zhou  ZHANG Xiao ying  LUO Guang hu  ZHU Jiang  Ning Xu  CAO Zhi fu  ZHANG Mao zu  ZHANG Yi
Affiliation:XU Xian-lin~
Abstract:ObjectiveTo investigate the expression of hepatic apolipoprotein M (apoM) mRNA and serum apoM during early stage of hepatic ischemia reperfusion injury in rats. MethodsRat models of hepatic (ischemia)-reperfusion injury (IRI) were established. Forty healthy male SD rats were randomly divived into five groups(each group containing eight rats):Sham-operation group(control); IRI groups, animals (experienced) 1 hr ischemia and then followed by various reperfusion intervals(0.5,1.0,2.0 and 3.0 hrs, respectively). ResultsSerum alanine-aminotransferase (ALT) levels and the liver injury degree (histologically) were increased with the prolongation of hepatic reperfusion time. The apoMmRNA level in liver was markedly decreased in the group that had reperfusion for 0.5hr compared to the sham group. However, it increased gradually in groups that had reperfusion for 1hr to 3hrs. Serum apoM protein level showed a (similar) tendency with apoMnRNA, but it increased after reperfusion for 2 hrs. ConclusionsIt is concluded that apoM expression pattern shows rapid and significant changes during hepatic ischemia-reperfusion injury, which suggests that apoM might have the characteristic of acute phase reactive protein.
Keywords:Liver Diseases  Reperfusion Injury  Disease Models  Animal  Apoliprotein M
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