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作 者:吴兴[1] 张海峰[1] 强晖[1] 陈海琴[1] 周国雄[1]
出 处:《南通大学学报(医学版)》2013年第1期31-34,共4页Journal of Nantong University(Medical sciences)
基 金:南通市社会发展基金资助项目(S5054)
摘 要:目的:探讨雷公藤内酯醇抑制CXCL11的表达对重症急性胰腺炎(severe acute pancreatitis,SAP)的治疗作用。方法:将72只SD大鼠随机分为3组:对照组,SAP组,雷公藤内酯醇治疗组,每组24只。牛黄胆酸钠建立SAP大鼠模型,治疗组予以雷公藤内酯醇治疗,分别检测各组不同时间点的血清淀粉酶,胰腺组织病理,免疫组化法、荧光定量检测胰腺CXCL11表达情况。结果:雷公藤内酯醇治疗组较SAP组血清淀粉酶值明显降低;胰腺病理与积分损伤减轻;胰腺免疫组化、荧光定量PCR提示雷公藤内酯醇治疗组较SAP组CXCL11表达明显减弱。结论:CXCL11参与了SAP发生发展,雷公藤内酯醇能显著抑制CXCL11的表达,减轻SAP时胰腺组织病理损伤。Objective: To investigate the effects of Triptolide by inhabit chemokine CXCLI 1 in severe acute pancreatitis(SAP). Methods: Seventy-two SD rats were randomly divided into three groups: control group (C group),SAP model group (P group), Triptolide treatment group(T group), and there were 24 rats in each group. SAP group was established by 4% sodium taurocholate. In T group,triptolide was injected into abdominal cavity immediately after the SAP model was sussessed. Serum amylase, the histolodic change of pancreas were measured at different time-point in each group. Protein in pancreas were decected by immunohistochemistry, and expression of CXCL11 mRNA in pancreas by fluorescence quantitative polymerase chain reaction. Results: Serum amylase and score of the histolodic change of pancreas were significantly lower in T group than P group at each time point, ImmunohistrochemistE~ and PCR showed expression of CXCL11 at each time point of T group were significantly lower compared with P group. Conclusions: CXCL11 may play an important role in the pathogenesis of SAP. Triptolide may ameliorate SAP and pancreatitis-associated complications by inhibiting the activity of CXCL11.
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