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中国临床药理学与治疗学 ›› 2012, Vol. 17 ›› Issue (8): 868-873.

• 基础研究 • 上一篇    下一篇

大鼠重症急性胰腺炎ENA-78的表达及生长抑素的干预作用

胡光龙1, 赵国海2   

  1. 1芜湖市第二人民医院急诊外科,芜湖 241000,安徽;
    2皖南医学院弋矶山医院胃肠外科,芜湖 241001,安徽
  • 收稿日期:2012-05-20 修回日期:2012-07-10 出版日期:2012-08-26 发布日期:2012-08-14
  • 通讯作者: 赵国海,男,本科,主任医师,教授,研究方向:外科危重症。Tel: 13505535899 E-mail: zhaoguohai@tom.com
  • 作者简介:胡光龙,男,硕士研究生,主治医师,研究方向:外科危重症。Tel: 13004063419 E-mail: hglhcy@163.com

Expression of ENA-78 in rats with severe acute pancreatitis and roles of somatostatin treatment

HU Guang-Long1, ZHAO Guo-Hai2   

  1. 1Department of Surgical Emergency, the Second People's Hospital of Wuhu, Wuhu 241001,Anhui;China;
    2Department of Gastrointestinal Surgery, Yijishan Hospital,Wannan Medical College,Wuhu 241001,Anhui, China
  • Received:2012-05-20 Revised:2012-07-10 Online:2012-08-26 Published:2012-08-14

摘要: 目的: 探讨趋化因子上皮中性粒细胞活化蛋白-78(ENA-78)在重症急性胰腺炎(SAP)大鼠早期发病机制中的作用,并观察生长抑素对ENA-78表达的影响。方法: 采用 3.5%牛磺胆酸钠胰胆管逆行注射制备SAP大鼠模型。SD大鼠随机分为假手术(SO)组、SAP 3 h、6 h、12 h 组和生长抑素(SST)干预 3 h、6 h、12 h 组。检测血清淀粉酶、胰腺髓过氧化物酶(MPO),光镜下观察胰腺病理组织学改变,采用逆转录-聚合酶链反应(RT-PCR)检测胰腺组织中ENA-78mRNA的表达,同时采用酶联免疫吸附法(ELISA)检测血清ENA-78的水平。结果: 与SO组相比,SAP组大鼠胰腺组织ENA-78 mRNA表达显著上调,并随SAP的加重ENA-78 mRNA表达逐渐增加(P<0.05 或 P<0.01); SAP各组大鼠血清中ENA-78水平明显高于SO组,并随SAP的加重逐渐增高(P<0.01);胰腺组织ENA-78 mRNA的水平与胰腺的病理损伤呈正相关(r=0.888,P<0.01);而经生长抑素干预后,SAP大鼠胰腺组织ENA-78 mRNA和血清ENA-78的水平明显下调。结论: ENA-78可能在SAP发生、发展过程中发挥重要作用;生长抑素可能通过抑制趋化因子ENA-78表达从而缓解SAP。

关键词: 重症急性胰腺炎, 趋化因子, 上皮中性粒细胞活化蛋白-78, 生长抑素

Abstract: AIM: To explore the potential role of ENA-78 on the pathogenesis during the early severe acute pancreatitis (SAP) in rats, and study the effect of somatostatin on ENA-78 expression.METHODS: Fifty-six SD rats were randomly divided into three groups: sham-operation group, SAP3 h, 6 h,12 h groups and somatostatin-treated 3 h, 6 h, 12 h groups.SAP was induced by retrograde injection 3.5% sodium taurocholate into the biliopancreatic duct.Somatostatin-treated groups were given somatostatin (20 μg/kg) intravenous injection after SAP model successfully established 0.5 h by microinjection pump.The levels of serum amylase and myeloperoxidase (MPO) in the pancreas tissue were tested. Pathological changes of pancreas were observed under the light microscopy.The ENA-78 mRNA expression of the pancreas tissue was analyzed by RT-PCR.The serum levels of ENA-78 were measured by means of enzyme-linked immunosobent assay (ELISA).RESULTS: Compared with SO group, the ENA-78 mRNA expression was up-regulated obviously in SAP group.During the process of SAP development from 3 h to 12 h, ENA-78 mRNA expression increased at 3 h and peaked at 12 h(P<0.05 or P<0.01, respectively).The serum levels of ENA-78 were significantly higher in SAP group than those in SO group (P<0.01).Furthermore, ENA-78 expression was positively correlated with the severity of pancreatic injury (r=0.888, P<0.01). After SST treatment, the mRNA expression and serum levels of ENA-78 declined significantly(P<0.05 or P<0.01,respectively)CONCLUSION: ENA-78 may play an important role in the pathogenesis of early SAP. Somatostatin has protective effect on SAP via down-regulating ENA-78 expression.

Key words: Severe acute pancreatitis, Chemotatic factor, Epithelial neutrohil-activating peptide-78, Somatostatin

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