实用肝脏病杂志 ›› 2010, Vol. 13 ›› Issue (2): 104-106.doi: 10.3969/j.issn.1672-5069.2010.02.008

• 论著 • 上一篇    下一篇

慢性乙型肝炎肝脏微循环障碍发生发展机制的研究

李志群, 张丰, 祝扬, 赵景民, 潘登, 杨建法, 赵雨来   

  1. 100094 北京市 解放军第261医院(李志群,张丰,祝扬); 解放军第302医院病理科 (赵景民,潘登,杨建法,赵雨来)
  • 收稿日期:2009-12-01 出版日期:2010-04-10 发布日期:2016-04-18
  • 作者简介:李志群 女,39岁,医学博士,副主任医师。E-mail:fairydoctor168167@yahoo.com.cn15min

A study on the mechanism of intrahepatic microcirculation changes in patients with chronic hepatitis B and cirrhosis

LI Zhiqun, ZHANG Feng, ZHU Yang, et al.   

  1. 261st Hospital,Beijing,100094
  • Received:2009-12-01 Online:2010-04-10 Published:2016-04-18

摘要: 目的 探讨慢性乙型肝炎患者肝脏微循环障碍的主要分子机制。方法 选择不同纤维化分期CHB穿刺肝组织和肝硬化外科活检肝组织及健康肝移植供体肝组织,应用免疫组化EliVisionTM System法,检测肝组织中COX1、COX2、AngII、AT1及α-SMA蛋白表达情况,并分析它们与肝内小血管、微血管或肝窦病理改变的关系。结果 在CHB肝组织内COX1、COX2、AngII、AT1、及α-SMA在血窦壁、肝内小的门静脉分支、肝动脉分支、中央静脉及小叶下静脉壁均呈不同程度的阳性表达,随肝纤维化程度的加重其表达水平明显升高,在活动期肝硬化肝组织内上述调节分子表达最强(x2=8.8535,P=0.0120)。结论 肝纤维化和肝硬化程度与COX1、COX2等指标之间存在相关性。

关键词: 乙型肝炎, 肝硬化, 环氧合酶, 血管紧张素

Abstract: Objective To explore main molecular mechanism of introhepatic microcirculation obstruction induced by chronic hepatitis B virus. Methods The liver biopsy tissues from patients with chronic hepatitis B,cirrhosis and healthy control were obtained. α-smooth muscle actin(α-SMA),cyclooxygenase2(COX2),COX1,and angiotensinII in the fibrotic livers and cirrhosis were examined by using immunohistochemistry. Results α-SMA,COX2,COX1 and angiotensin II in hepatic sinusoidal wall,little portal venules branch,hepatic arteries branch,central vein,vein wall beneath lobules were positive. They were obviously up-regulated as compared to control. Conclusions Intrahepatic microcirculation changes was found in chronic hepatitis B and cirrhosis.

Key words: Liver cirrhosis, Hepatitis B, Cyclooxygenase, AngiotensinII