[An experimental model of hepatic fibrosis induced by alcohol and CCl4: can the lipopolysaccharide prevent liver injury induced by alcohol and CCl4?].

Hee Bok Chae, Lee Chan Jang, Seon Mee Park, Bo Ra Son, Rohyun Sung, Jae Woon Choi
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Abstract

Background/aims: It is well known that alcohol enhances the toxicity of CCl4. We tried to establish an alcoholic liver cirrhosis model by administration of alcohol and CCl4 to rats. We also wanted to know the hepatoprotective effect of low doses of lipopolysaccharide(LPS) in this animal model.

Methods: Of 20 female adult rats, 8 were ingested with alcohol ad libitum(group 1) Another 6 were ingested with 10% alcohol and 50% 1mL/kg CCl4 intragastrically by Sonde twice a week(group 2) The remaining 6 were ingested with 10% alcohol, CCl4, and 0.1mg/kg LPS intraperitoneally twice a week(group 3) The fibrosis was evaluated semiquantitatively on a scale of 0(none) to 3(cirrhosis).

Results: 1) After 10 weeks, septal fibrosis or cirrhosis was produced in 9 out of 12 rats in groups 2 and 3 but there was no fibrotic change in group 1. 2) There was no significant difference in pathological grading between groups 2 and 3.

Conclusions: Hepatic fibrosis or cirrhosis can be sufficiently induced by alcohol and repetitive CCl4 ingestion for 10 weeks. We can not prove the hepatoprotective effect of low dose LPS by semiquantitative evaluation of pathological grading.

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[酒精和CCl4致肝纤维化实验模型:脂多糖能否预防酒精和CCl4致肝损伤?]。
背景/目的:众所周知,酒精可增强CCl4的毒性。我们试图通过给药酒精和CCl4建立大鼠酒精性肝硬化模型。我们还想知道低剂量脂多糖(LPS)在动物模型中的肝保护作用。方法:雌性成年大鼠20只,8只自由酒精灌胃(1组),6只Sonde腹腔灌胃10%酒精和50% CCl4 1mL/kg(2组),其余6只腹腔灌胃10%酒精、CCl4和0.1mg/kg LPS, 1周2次(3组),按0(无)~ 3(肝硬化)进行半定量评价。结果:1)10周后,2、3组12只大鼠中有9只出现间隔纤维化或肝硬化,1组无纤维化改变。2) 2组和3组的病理分级无显著差异。结论:连续10周反复摄入CCl4可充分诱导肝纤维化或肝硬化。我们不能通过病理分级的半定量评价来证明低剂量LPS的肝保护作用。
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