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作 者:吴灵飞[1] 冯家琳[1] 李国平 蒲泽锦[1] 苏剑东[1]
机构地区:[1]汕头大学医学院第二附属医院消化内科,广东汕头515041
出 处:《汕头大学医学院学报》2007年第1期24-27,F0003,共5页Journal of Shantou University Medical College
基 金:广东省中医药管理局资助项目(103066)
摘 要:目的:研究胃舒散对消炎痛所致大鼠小肠损伤的保护作用及机制。方法:皮下注射消炎痛(10 mg/kg)制作大鼠小肠损伤模型。用光镜、扫描电镜和透射电镜观察不同剂量[3.0、1.5、0.75 g/(kg.d)]胃舒散对小肠损伤的影响,同时检测小肠黏膜髓过氧化物酶(MPO)、超氧化物歧化酶(SOD)活性和丙二醛(MDA)含量以及血清NO含量。结果:消炎痛引起明显的小肠黏膜损伤,伴有NO、MPO、MDA含量增加及SOD活性下降(P<0.05,P<0.01)。胃舒散剂量依赖性地减少小肠黏膜损伤指数,提高了胃组织SOD活性(P<0.05)、降低了MPO、MDA含量(P<0.05),但对血清NO水平无明显影响(P>0.05)。结论:氧自由基及NO参与了消炎痛所致小肠黏膜的损伤,胃舒散对此病变有明显保护作用,其机制与抗氧化作用有关。Objective: To study the protective effect of Weishusan on small intestinal lesions induced by indomethacin in rats. Methods: Wistar rats were injected indomethacin(suspension 10 mg/kg)subeutaneously, and the small intestine was examined for lesions 24 hours later. The different doses[3.0, 1.5, 0.75 g/( kg·d) ] of Weishusan were administered i.g. twice, intestinal mucosal changes were observed by quantitative histology, scanning electron microscopy and transmisson electron microscopy. Superoxide dismutase ( SOD ), myeloperoxidase(MPO) activities and malondialdehyde (MDA)levels in intestinal tissues and nitric oxide(NO)levels in senan were determined. Results: Severe lesions in the jejunum and ileum were caused by indomethacin and the NO, MPO and MDA contents were markedly increased( P 〈 0.05). Weishusan dose-dependently prevented the intestinal lesions( P 〈 0.05), enhanced SOD activities( P 〈 0.05) and decreased MPO and MDA levels(P 〈 0.05) but not affected NO levels(P 〉 0.05). Conclusion: Oxygen free radicals and NO may play important roles in intestinal lesions induced by indomethacin. Weishusan can protect the small intestine by antioxidation mechanism.
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