文章摘要
张宏伟,石莎,卢克美.替普瑞酮及雷贝拉唑对急性胃黏膜损伤大鼠TFF3表达的研究[J].安徽医药,2015,19(12):2280-2283.
替普瑞酮及雷贝拉唑对急性胃黏膜损伤大鼠TFF3表达的研究
Expression of TFF3 in rats with acute gastric mucosal lesion treated by Teprenone and Rabeprazole
投稿时间:2015-07-29  
DOI:
中文关键词: 替普瑞酮  雷贝拉唑  急性胃黏膜病变  三叶草因子3  保护性作用
英文关键词: teprenone  rabeprazole  acute gastric mucosal lesion  trefoil factor 3  protection
基金项目:聊城市科学技术攻关计划项目(No 2014-2-134)替普瑞酮及雷贝拉唑对急性胃黏膜损伤大鼠TFF3表达的研究张宏伟1,石莎2,卢克美2
作者单位
张宏伟 药剂科 
石莎 消化内科,山东 聊城 252000 
卢克美 消化内科,山东 聊城 252000 
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中文摘要:
      目的 研究替普瑞酮及雷贝拉唑对无水乙醇诱发大鼠急性胃黏膜病变的保护性作用及三叶草因子3(TFF3)的表达。方法 将大鼠按体重随机分为5 组,分为正常对照组、模型组、替普瑞酮治疗组、雷贝拉唑治疗组、替普瑞酮联合雷贝拉唑治疗组(联合治疗组),每组8 只。用无水乙醇制备大鼠急性胃黏膜病变模型,苏木精—伊红染色观察各组大鼠胃黏膜组织病理学改变,免疫组织化学法测定各组大鼠胃黏膜TFF3的表达情况。结果 与模型组比较,各药物治疗组胃黏膜溃疡指数明显减少,有显著性差异(P<0.01);与替普瑞酮治疗组比较,联合治疗组胃黏膜溃疡指数明显减少,有统计学意义(P<0.05);与雷贝拉唑治疗组比较,联合治疗组胃黏膜溃疡指数明显减少,有显著性差异(P<0.01)。HE染色结果,与正常对照组比较,模型组大鼠的胃黏膜表面上皮细胞缺失,伴随大量炎症细胞浸润,肌层和浆膜被破坏;与模型组比较,雷贝拉唑、替普瑞酮治疗组及联合治疗组的大鼠胃黏膜表层上皮细胞缺失减少,黏膜腺体重现,浆膜结构较完整,且炎症细胞较少。免疫组织化学结果,与正常对照组比较,模型组及各药物治疗组胃黏膜TFF3的表达显著增多(P<0.05)。与雷贝拉唑组比较,联合治疗组大鼠胃溃疡周边TFF3的阳性细胞密度明显增加(P<0.05)。结论 替普瑞酮与雷贝拉唑可能通过上调 TFF3 的表达改善无水乙醇所致大鼠胃黏膜组织损伤,促进胃黏膜的愈合,对大鼠急性胃黏膜病变起到保护作用。
英文摘要:
      Objective To explore the expression of TFF3 and the protective role of Teprenone and Rabeprazole in rats with acute gastric mucosal lesion. Method Forty wistar male rats were randomly assigned into normal control group, model group, teprenone group, rabeprazole group and teprenone/rabeprazole group, with 8 rats in each group. Acute gastric mucosal lesion model was induced by absolute ethylalcohol. Gastric tissue pathological changes were performed by hematoxylineosin staining,and gastric ulcer index was evaluated.Expression of TFF3 in gastric mucosa was detected by immune histochemical method. Results (1) UI of drug treatment groups was significantly lower than that of model group(P<0.01); UI of combination group was lower than that of teprenone group(P<0.05);UI of combination group was lower than that of rabeprazole group(P<0.01).(2) Hematoxylineosin staining results were as follows:Compared with control group, epithelial cells were deficient on gastric mucosa surface in model group, with a large number of inflammatory cells infiltration as well as muscularis and serosa destroyed; By comparison with model group, in rabeprazole group, teprenone group and rabeprazole/teprenone group deficiency of epithelial cells of gastric mucosa surface was less, mucous glands reappeared, and serous membrane structure was relatively complete with less inflammatory cells and exudate.(3)Immunohistochemical results were as follows:Expression of TFF3 positive cells in model group and drug intervention group was significantly increased, which was significantly higher than that in normal control group(P<0.05). Conclusion Rabeprazole and teprenone may protect gastric mucosa tissues by raising TFF3 expression,promote the healing of gastric mucosa and alleviate the acute gastric mucosa injury in rats.
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