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Study of heteroserum-induced rat liver fibrosis model and its mechanism 被引量:22
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作者 HUANG Zhi Gang, ZHAI Wei Rong, ZHANG Yue E and ZHANG Xiu Rong 《World Journal of Gastroenterology》 SCIE CAS CSCD 1998年第3期26-29,共4页
AIM To investigate the morphological changes in the process of heteroserum induced rat liver fibrosis and the mechanism of fibrogenesis of this model. METHODS A model of heteroserum induced rat liver fibrosis was... AIM To investigate the morphological changes in the process of heteroserum induced rat liver fibrosis and the mechanism of fibrogenesis of this model. METHODS A model of heteroserum induced rat liver fibrosis was established by intraperitoneal injection of porcine serum. In addition to the observation of the morphological changes of this model, the infiltration of eosinophils and mast cells were measured quantitatively and the deposition of IgG and complement C 3 was detected by immunofluorescence. RESULTS The rat liver fibrosis was induced successfully at the end of the 8th week after the injection of heteroserum. Besides the increase of hepatic stellate cells (HSC) during the process of liver fibrosis, proliferation and activation of primary mesenchyma cells (PMCs) were also found. In the early stage, the infiltration of eosinophils and mast cells was significantly increased and the deposition of IgG and complement C 3 was positive in the portal tracts and septa, while gradually reduced after the injection was stopped. CONCLUSIONS This model is suitable for the research on liver fibrogenesis; the pathogenesis of this model may be related with the allergen induced late phase reaction (LPR) caused by the injection of heteroserum, and the HSCs and the PMCs are important sources of ECM producing cells. 展开更多
关键词 liver CIRRHOSIS heteroserum disease models animal liver/pathology MAST cell IgG COMPLEMENT C 3 rats
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As_(2)O_(3)对大鼠BRL-3A和RH-35细胞TRβ1和Cyclin D1因子的影响 被引量:1
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作者 王炼 王雪飞 +6 位作者 刘丹 耿敏杰 郭志伟 崔娜 刘建平 夏雅娟 杨英 《中国兽医学报》 CAS CSCD 北大核心 2023年第4期741-747,共7页
为了探明As_(2)O_(3)对大鼠肝脏细胞系BRL-3A和肝癌细胞系RH-35中TH信号通路的关键调控因子TRβ1和TRβ1的下游因子Cyclin D1的影响,采用qRT-PCR、Western blot技术检测2种细胞中TRβ1和Cyclin D1的基因和蛋白表达变化。结果显示:(1)与... 为了探明As_(2)O_(3)对大鼠肝脏细胞系BRL-3A和肝癌细胞系RH-35中TH信号通路的关键调控因子TRβ1和TRβ1的下游因子Cyclin D1的影响,采用qRT-PCR、Western blot技术检测2种细胞中TRβ1和Cyclin D1的基因和蛋白表达变化。结果显示:(1)与对照组相比,As_(2)O_(3)作用BRL-3A细胞12h,1.563μmol/L组TRβ1蛋白表达显著降低(P<0.01)、Cyclin D1表达显著升高(P<0.01);6.250μmol/L组TRβ1表达明显降低(P<0.05)、Cyclin D1表达显著降低(P<0.01)。As_(2)O_(3)作用24h,1.563μmol/L组TRβ1蛋白表达明显升高(P<0.05);6.250μmol/L组TRβ1显著升高(P<0.01),Cyclin D1的表达显著降低(P<0.01)。As_(2)O_(3)作用48h,6.250μmol/L组TRβ1蛋白表达显著升高(P<0.01),各组Cyclin D1表达均显著降低(P<0.01)。基因表达结果与蛋白表达结果基本一致。(2)与对照组相比,As_(2)O_(3)作用RH-35细胞12h,各组TRβ1蛋白表达量显著升高(P<0.01)。As_(2)O_(3)作用RH-3524h,1.563μmol/L组TRβ1蛋白表达量明显升高(P<0.05),其余组显著升高(P<0.01)。As_(2)O_(3)作用48h,3.125和6.250μmol/L组TRβ1蛋白表达显著升高(P<0.01),1.563μmol/L组明显降低(P<0.05)。As_(2)O_(3)作用RH-3512,24,48h,各组Cyclin D1蛋白表达量均显著降低(P<0.01)。基因结果与蛋白结果基本一致。表明As_(2)O_(3)随着作用时间的增加,引起大鼠肝脏细胞系BRL-3A和肝癌细胞系RH-35TRβ1的水平异常,进而干扰Cyclin D1的水平。 展开更多
关键词 三氧化二砷 大鼠肝脏细胞系brl-3a 大鼠肝癌细胞系RH-35 甲状腺激素受体β1 细胞周期蛋白D1
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肠三叶因子对非酒精性脂肪性肝炎大鼠回肠黏液屏障的影响 被引量:3
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作者 梁凯 孔维宗 +1 位作者 陈娟 王迎春 《临床肝胆病杂志》 CAS 2017年第8期1552-1557,共6页
目的研究非酒精性脂肪性肝炎(NASH)大鼠肠道黏液屏障改变,探讨肠三叶因子(TFF3)对NASH大鼠肠道黏液屏障的影响,及其对NASH的治疗作用。方法将清洁级雄性SD大鼠60只随机分为正常组、模型组和治疗组,每组20只。正常组给予普通饲料,模型组... 目的研究非酒精性脂肪性肝炎(NASH)大鼠肠道黏液屏障改变,探讨肠三叶因子(TFF3)对NASH大鼠肠道黏液屏障的影响,及其对NASH的治疗作用。方法将清洁级雄性SD大鼠60只随机分为正常组、模型组和治疗组,每组20只。正常组给予普通饲料,模型组和治疗组给予高脂饲料12周,诱导NASH模型后,治疗组给予rh TFF3 1 ml·kg^(-1)·d^(-1)(浓度0.1 mg/ml)腹腔内注射,正常组与模型组给予1 ml·kg^(-1)·d^(-1)生理盐水,连续3周。第15周末,FITC标记的右旋糖酐灌胃检测大鼠回肠通透性后,处死大鼠,检测血清AST、ALT、TC、TG、内毒素(ET)水平及二胺氧化酶(DAO)活性。HE染色观察肝脏和回肠末端组织病理变化,PAS染色观察回肠末端杯状细胞并计数,免疫组化方法检测回肠末端紧密连接蛋白Occludin和TFF3蛋白表达水平,实时荧光定量PCR检测TFF3 mRNA转录水平。计量资料多组间比较采用单因素方差分析,进一步两两比较采用LSD-t检验。结果大鼠血清AST、ALT、TG、TC、DAO、ET水平在模型组升高,而治疗组较模型组明显下降(P值均<0.01);模型组NAS评分较正常组显著增高(P<0.01),而治疗组肝组织炎症改善,NAS评分较模型组明显降低(P<0.01);光镜下模型组回肠末端细胞坏死,绒毛损伤,杯状细胞明显减少,治疗组绒毛损伤修复,杯状细胞增多;模型组大鼠回肠通透性与正常组比显著增加,治疗组较模型组明显降低(P值均<0.01);Occludin和TFF3在模型组表达减少,而治疗组较模型组增多(P值均<0.01);回肠末端TFF3 mRNA转录水平模型组较正常组下调,治疗组表达较模型组上调(P值均<0.01)。结论 NASH大鼠存在肠道杯状细胞损伤,黏液屏障功能障碍,TFF3可以修复回肠末端损伤,促进杯状细胞再生与黏液分泌,修复肠屏障功能,降低肠通透性,对NASH起到治疗作用。 展开更多
关键词 脂肪肝 肠三叶因子 杯状细胞 大鼠 Sprague-Dawley
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