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作 者:辛振磊[1] 胡杰[1] 闫盛[1] 王玉文[1] 刘新奇[1] 张超[1] 李海峰[1] 苏磊[1] 董红霖[1]
机构地区:[1]山西医科大学第二医院血管外科,太原030001
出 处:《中华肝胆外科杂志》2014年第5期380-383,共4页Chinese Journal of Hepatobiliary Surgery
基 金:山西省科技攻关项目(201303130174)
摘 要:目的建立大鼠急性胰腺炎(AP)模型,观察外源性中介素8-47(IMD8-47)干预前后胰腺内、外分泌部微循环血管内皮细胞的变化,探讨IMD8-47对AP大鼠胰腺内、外分泌部微循环的影响。方法皮下注射蛙皮素建立大鼠AP模型:(1)检测各组大鼠胰腺水肿程度及血清淀粉酶含量;(2)光镜下观察各组胰腺组织病理学改变;(3)透射电镜观察胰腺内、外分泌部微循环血管内皮细胞超微结构变化;(4)免疫组化法检测胰腺内、外分泌部微循环血管内皮型一氧化氮合酶(eNOS)及血管内皮钙粘蛋白(VE-cadherin)表达情况。结果(1)胰腺组织水肿程度、病理评分及淀粉酶检测:AP组较IMD8-47干预组差异有统计学意义(P=0.035);(2)干预前后胰腺内、外分泌部毛细血管内皮细胞超微结构发生改变;(3)免疫组化显示:对照组、干预组及模型组胰腺毛细血管内膜eNOS和VE—eadherin的含量内、外分泌部均有改变,差异有统计学意义(P〈0.05)。结论外源性IMD8-47能够对胰腺组织起到保护作用,但对胰腺内、外分泌部的影响存在差异。Objective To establish rat model of acute pancreatitis and observe the influence of Intermedin8-47 (IMD8-47) on microcirculation endothelial cell in the exocrine and endocrine parts of pancreas. Methods Rat model of acute pancreatitis is established by subcutaneous injection of bombesin : ( 1 ) Evaluation of pancreatic edema and detection of the serum amylase level ; ( 2 ) Pathology observation of pancreatic tissue by Light-microscopy ; (3) Observation of ultrastructure changes of microcirculation endothelial cell in the parts of exocrine and endocrine by transmission electron microscope (TEM) ; (4) Detection of the expression of eNOS and VE-cadherin in endothelial cells by immune histochemical method. Results ( 1 ) Compared with IMD8-47 intervention group, AP Group had more serious edema, higher level of serum amyl- ase and pathological score of pancreatic tissue. The difference between the two groups was statistically significant (P = 0. 035) ; (2) TEM showed that after exogenous IMD8-47 intervention, the ultrastructure of blood capillary endothelial cells in the parts of exocrine and endocrine changed significantly ; ( 3 ) Immunohistochemical section showed that the eNOS and VE - cadherin expressions was significantly different among Control group, IMD8-47 intervention group and AP model group (P 〈 0.05 ). Conclusion Exogenous IMD8-47 may contribute to protecting pancreatic tissue by the different effects on pancreatic exocrine and endocrine parts.
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