首页> 外文期刊>World Journal of Gastroenterology >Pathological mechanisms of alcohol-induced hepatic portal hypertension in early stage fibrosis rat model.
【24h】

Pathological mechanisms of alcohol-induced hepatic portal hypertension in early stage fibrosis rat model.

机译:酒精引起的肝门静脉高压症早期纤维化大鼠模型的病理机制。

获取原文
获取原文并翻译 | 示例
           

摘要

AIM: To study the role of hepatic sinusoidal capillarization and perisinusoidal fibrosis in rats with alcohol-induced portal hypertension and to discuss the pathological mechanisms of alcohol-induced hepatic portal hypertension. METHODS: Fifty SD rats were divided into control group (n=20) and model group (n=30). Alcoholic liver fibrosis rat model was induced by intragastric infusion of a mixture containing alcohol, corn oil and pyrazole (1 000:250:3). Fifteen rats in each group were killed at wk 16. The diameter and pressure of portal vein were measured. Plasma hyaluronic acid (HA), type IV collagen (CoIV) and laminin (LN) were determined by radioimmunoassay. Liver tissue was fixed in formalin (10%) and 6-mum thick sections were routinely stained with Mallory and Sirius Red. Liver tissue was treated with rabbit polyclonal antibody against LN and ColIV. Hepatic non-parenchymal cells were isolated, total protein was extracted and separated by SDS-PAGE. MMP-2 and TIMP-1 protein expression was estimated by Western blotting. RESULTS: The diameter (2.207+/-0.096 vs 1.528+/-0.054 mm, P<0.01) and pressure (11.014+/-0.395 vs 8.533+/-0.274 mmHg, P<0.01) of portal vein were significantly higher in model group than those in the control group. Plasma HA (129.97+/-16.10 vs 73.09+/-2.38 ng/mL, P<0.01), ColIV (210.49+/-4.36 vs 89.65+/-4.42 ng/mL, P<0.01) and LN (105.00+/-7.29 vs 55.70+/-4.32 ng/mL, P<0.01) were upregulated in model group. Abundant collagen deposited around the central vein of lobules, hepatic sinusoids and hepatocytes in model group. ColI and ColIII increased remarkably and perisinusoids were almost surrounded by ColIII. Immunohistochemical staining showed that ColIV protein level (0.130+/-0.007 vs 0.032+/-0.004, P<0.01) and LN protein level (0.152+/-0.005 vs 0.029+/-0.005, P<0.01) were up-regulated remarkably in model group. MMP-2 protein expression (2.306+/-1.089 vs 0.612+/-0.081, P<0.01) and TIMP-1 protein expression (3.015+/-1.364 vs 0.446+/-0.009, P<0.01) in freshly isolated hepatic non-parenchymalcells were up-regulated in model group and TIMP-1 protein expression was evidently higher than MMP-2 protein expression (2.669+/-0.170 vs 1.695+/-0.008, P<0.05). CONCLUSION: Hepatic sinusoidal capillarization and peri-sinusoidal fibrosis are responsible for alcohol-induced portal hypertension in rats.
机译:目的:研究肝窦毛细血管化和肝窦周围纤维化在酒精性门静脉高压症大鼠中的作用,探讨酒精性肝门静脉高压症的病理机制。方法:50只SD大鼠分为对照组(n = 20)和模型组(n = 30)。酒精性肝纤维化大鼠模型是通过在胃内输注含有酒精,玉米油和吡唑的混合物(1 000:250:3)诱导的。第16周每组杀死15只大鼠。测量门静脉的直径和压力。通过放射免疫测定法测定血浆透明质酸(HA),IV型胶原(CoIV)和层粘连蛋白(LN)。将肝组织固定在福尔马林(10%)中,并用Mallory和Sirius Red常规染色6毫米厚的切片。用抗LN和ColIV的兔多克隆抗体处理肝组织。分离肝非实质细胞,提取总蛋白并通过SDS-PAGE分离。通过蛋白质印迹法评估MMP-2和TIMP-1蛋白的表达。结果:模型中门静脉的直径(2.207 +/- 0.096 vs.1.528 +/- 0.054 mm,P <0.01)和压力(11.014 +/- 0.395 vs 8.533 +/- 0.274 mmHg,P <0.01)在模型中明显更高组比对照组。血浆HA(129.97 +/- 16.10 vs 73.09 +/- 2.38 ng / mL,P <0.01),ColIV(210.49 +/- 4.36 vs 89.65 +/- 4.42 ng / mL,P <0.01)和LN(105.00 + /模型组上调-7.29 vs 55.70 +/- 4.32 ng / mL,P <0.01)。模型组小叶中央静脉,肝窦,肝细胞周围大量胶原沉积。 ColI和ColIII显着增加,并且周围的类固醇几乎被ColIII包围。免疫组织化学染色显示ColIV蛋白水平(0.130 +/- 0.007 vs 0.032 +/- 0.004,P <0.01)和LN蛋白水平(0.152 +/- 0.005 vs 0.029 +/- 0.005,P <0.01)显着上调在模型组中。新鲜分离的非肝细胞MMP-2蛋白表达(2.306 +/- 1.089 vs.0.612 +/- 0.081,P <0.01)和TIMP-1蛋白表达(3.015 +/- 1.364 vs 0.446 +/- 0.009,P <0.01)模型组肝实质细胞上调,TIMP-1蛋白表达明显高于MMP-2蛋白表达(2.669 +/- 0.170对1.695 +/- 0.008,P <0.05)。结论:肝窦毛细血管化和正弦周围纤维化是酒精引起的大鼠门脉高压的原因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号