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作 者:田茸[1] 巩子汉 杨晓轶[2] 朱立鸣[2] 段永强[2] 成映霞[2] 杜娟[2] 王燕[2]
机构地区:[1]成都中医药大学,成都611137 [2]甘肃中医学院,兰州730020
出 处:《中国中医基础医学杂志》2016年第4期468-471,共4页JOURNAL OF BASIC CHINESE MEDICINE
基 金:国家自然科学基金资助项目(81160420);甘肃省自然科学基金资助项目(1010RJZA148);甘肃省教育厅基金资助项目(1006-05)
摘 要:目的:从Ca M信号通路关键基因揭示脾气虚证发生及益气健脾法干预作用机制。方法:脾气虚证大鼠为研究对象,采用实时荧光定量RT-PCR、Western Blot技术检测不同阶段大鼠脑、肠Ca M信号通路关键基因Ca M/Ca MKⅡmRNA和蛋白的动态表达,并分析四君子汤干预效应机制。结果:从大鼠小肠组织看,脾气虚证大鼠相对于正常大鼠Ca M/Ca MKⅡmRNA和蛋白表达升高,经四君子汤治疗后明显降低;从大鼠脑组织看,脾气虚证大鼠相对于正常大鼠Ca M/Ca MKⅡmRNA和蛋白表达降低,经四君子汤治疗后明显升高。结论:脑肠微环境中Ca M信号传导通路关键基因Ca M/Ca MKⅡ的动态表达与脾气虚证形成有关,四君子汤通过影响其表达对脾气虚证起到时相性动态干预。Objective : To reveal the mechanism about the expressions of key genes of CaM signal pathway of the spleen qi deficiency rats, and the intervention effects about strengthening spleen and benefiting qi. Methods: We took the spleen qi deficiency rats as the targets, We detected dynamic expressions of critical genes CaM/CaMK I1 mRNA and protein on CaM signaling pathway in brain and intestine microenvironments at different time by technique methods of real-time quantitative RT-PCR and Western Blot. At the same time we studied on the intervention effect mechanism of Sijunzi Decoction to treat spleen qi deficiency rats. Results:l Rat intestinal detection index: Spleen qi deficiency rats intestinal CaM/CaMK Ⅱ mRNA and proteins expressions increased compared with normal rats. After the treatment of Sijunzi Decoction rats intestinal CaM/ CaMK Ⅱ mRNA and proteins expressions reduced compared with spleen qi deficiency rats. 2 Rat brain detection index: Spleen qi deficiency rats brain CaM/CaMK Ⅱ mRNA and proteins expressions reduced compared with normal rats. After the treatment of Sijunzi Decoction rats brain CaM/CaMK Ⅱ mRNA and proteins expressions increased compared with spleen qi deficiency rats. Conclusions: The dynamic expressions of key genes CaM/CaMK Ⅱ of CaM signal pathway in brain and intestine microenvironment, which is the basis for spleen qi deficiency syndrome. Sijunzi Decoction treated spleen qi deficiency by affecting the dynamic expressions of CaM/CaMK Ⅱ.
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