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作 者:徐靖宇[1] 白威峰[2] 涂平[2] 刘兴宇[2] 余守洋[2] 罗素元[2]
机构地区:[1]遵义医学院附属医院消化内科,贵州省遵义市563099 [2]遵义医学院细胞生物学与遗传学教研室,贵州省遵义市563003
出 处:《世界华人消化杂志》2015年第7期1110-1114,共5页World Chinese Journal of Digestology
基 金:国家自然科学基金资助项目;No.30860373~~
摘 要:目的:探讨吗啡依赖胃肠损伤的多巴胺(dopamine,DA)能作用机制.方法:吗啡剂量递增皮下注射训练10 d,建立大鼠吗啡条件性位置偏爱(conditioned place preference,CPP)模型,生理盐水对照组(normal saline,NS)组和吗啡模型组(模型组)各取10只断头处死,取胃和十二指肠黏膜,荧光分光光度法检测其DA含量;另再取10只,采用Western blot检测其胃(胃贲门、胃体和幽门)和十二指肠组织多巴胺受体亚型2(dopamine D2 receptor,D2R)蛋白的表达.两组计量资料比较采用t检验.结果:模型组大鼠胃、十二指肠D A含量(18.41 n g/g±0.62 n g/g、9.01 n g/g±2.37ng/g)较NS组(32.01 ng/g±0.61 ng/g、17.31ng/g±2.58 ng/g)显著减少(胃:t=49.765,P=0.000;十二指肠:t=7.485,P=0.000);而模型组胃贲门、胃体和十二指肠的D2R平均光密度值(0.67±0.05、0.53±0.08和0.61±0.07)较NS组(0.43±0.08、0.33±0.07和0.44±0.05)明显升高(胃贲门:t=7.557,P=0.001;胃体:t=6.859,P=0.000;十二指肠:t=6.188,P=0.001);胃幽门变化差异无统计学意义(t=0.84,P=0.43).结论:吗啡依赖胃肠的损伤与胃肠DA系统的改变(递质和D2R受体)具有一定的相关性.AIM: To investigate the mechanism of action of dopamine in gastrointestinal injury in morphine-dependent rats.METHODS: A conditioned place preference(CPP) model was established by injecting rats with increasing doses of morphine. The rats were divided into two groups: a model group(M) and a saline group(N). Ten rats in each group were killed to detect the DA contents in the stomach and duodenum with a fluorescence spectrophotometer. The other 10 rats were used to test the expression levels of D2 receptor in the gastric cardia, body, pylorus and duodenum by Western blot. RESULTS: The expression of DA in the stomach and duodenum was significantly lower in the model group than in the control group(18.41 ng/g ± 0.62 ng/g vs 32.01 ng/g ± 0.61 ng/g, 9.01 ng/g ± 2.37 ng/g vs 17.31 ng/g ± 2.58 ng/g, P〈0.01). The expression of D2 R in the gastric cardia, gastric body and duodenum was significantly higher in the morphine dependent group than in the control group(0.67 ± 0.05 vs 0.43 ± 0.08, 0.53 ± 0.08 vs 0.33 ± 0.07, 0.61 ± 0.07 vs 0.44 ± 0.05, P〈0.01). CONCLUSION:There is an obvious link between the pathological injury in gastrointestinal tissue and the DA system change in morphine-dependent rats.
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