己酮可可碱对大鼠胰腺纤维化及TGFβ1、αSMA、MMP1、TIMP1表达的影响
己酮可可碱·间质胶原酶·金属蛋白酶1组织抑制剂·转化生长因子β·α平滑肌肌动蛋白·胰腺炎·纤维化·大鼠,Wistar,,己酮可可碱·间质胶原酶·金属蛋白酶1组织抑制剂·转化生长因子β·α平滑
【摘要】目的:探讨己酮可可碱(PTX)对大鼠胰腺纤维化及TGFβ1、αSMA、MMP1、TIMP1表达的影响。方法:通过胰管内注射2%三硝基苯磺酸的方法制备大鼠胰腺纤维化模型。随机分为对照组、模型组、PTX干预组。PTX干预组于术后第2天给予PTX腹腔注射,6mg/(kg·d),4周后收集各组胰腺标本。免疫组化SABC法检测各组胰腺组织中α平滑肌肌动蛋白(αSMA)、转化生长因子β1(TGFβ1)、基质金属蛋白酶1(MMP1)、金属蛋白酶组织抑制物1(TIMP1)的表达同时做组织胶原纤维染色。部分胰腺组织液氮冻存,以Western blot方法检测αSMA的表达。结果:模型组发生胰腺纤维化,PTX干预组有轻度纤维化。PTX干预组αSMA、TGFβ1、TIMP1的表达均低于模型组(P<0.01)。MMP1的表达无明显差异。PTX干预组胶原面积百分比明显低于模型组(P<0.01)。结论:PTX抗大鼠胰腺纤维化的作用可能与其降低TGFβ1、αSMA、TIMP1表达有关。【关键词】己酮可可碱·间质胶原酶·金属蛋白酶1组织抑制剂·转化生长因子β·α平滑肌肌动蛋白·胰腺炎·纤维化·大鼠,Wistar
Effect of pentoxifylline on the expressions of TGFβ1,αSMA,MMP1 and TIMP1 in rat pancreatic fibrosis
WANG Dongsheng1,LIU Qian2
1Department of Interventional Radiology,Coal General Hospital(Beijing 100028,China)
2Department of Digestion,Shandong Provincial Qianfoshan Hospital(Jinan 250014,
China)
【ABSTRACT】Objective:To observe the effect of pentoxifylline on pancreatic fibrosis and the expressions of TGFβ1,αSMA,MMP1 and TIMP1 in rat.Methods:The injection method of 2% TNBS through rats’s pancreatic duct was undertaken to set up the animal model of pancreatitis,Mice of interventional group were treated with PTX,and the samples of pancreas were collected after 4 weeks treatment for evaluating the expression of TGFβ1,αSMA,MMP1 and TIMP1 by using immunohistochemistry technique.Masson staining of pancreas were undertaken.The expression of αSMA in some samples were evaluated by using Western blot.Results:Pancreas fibrosis was observed in model group rats and there were no significant pancreas fibrosis in PTX interventional group.PTX interventional significantly reduced the content of TGFβ1,αSMA,and TIMP1 compared to the model(P<0.01),while that of MMP1 was unchanged in PTX interventionalgroup.Pancreas fibrosis proportion was also reduced in PTX interventional group(P<0.01).Conclusion:PTX could inhibit the formation of pancreas fibrosis in rats,which might relate to the decreasing expression of TGFβ1,αSMA,TIMP1. ......
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