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大黄素对2型糖尿病大鼠胃动力的影响及机制研究
引用本文:李艳芬,严祥,赵丽,陈明,张新华.大黄素对2型糖尿病大鼠胃动力的影响及机制研究[J].中国药房,2008,19(15):1135-1138.
作者姓名:李艳芬  严祥  赵丽  陈明  张新华
作者单位:[1]兰州大学第一医院老年病科,兰州市730000; [2]兰州大学第一医院中心实验室,兰州市730000; [3]兰州大学第一医院核医学科,兰州市730000
摘    要:目的:研究大黄素对2型糖尿病大鼠胃动力的影响及其机制。方法:以小剂量链脲佐菌素(STZ,30mg·kg-1)加长期高脂高糖饲料喂养复制大鼠2型糖尿病模型。复制成功后分别用大黄素、替加色罗、多潘立酮进行药物干预治疗6周,并设立正常对照组与模型组进行同期比较。实验结束时用单光子发射计算机断层扫描技术(SPECT)测定胃半排空时间(GET1/2)与90min胃内核素残留率(RIH);常规检测空腹血糖、血清胰岛素、三酰甘油(TG)、总胆固醇(TC)、高密度脂蛋白-胆固醇(HDL-C);并用放免法检测血浆和胃肠组织P物质(SP)、生长抑素(SS)的含量。结果:模型组大鼠的胃排空较正常对照组显著减慢(P<0·01),而大黄素、替加色罗及多潘立酮组大鼠的胃排空较模型组显著加快(P<0·01或P<0·05)。大黄素、替加色罗及多潘立酮组大鼠的血浆和胃肠组织SP较模型组显著升高,而SS显著降低(P<0·01或P<0·05)。模型、替加色罗及多潘立酮组大鼠血清TG和TC较正常对照组显著升高,而HDL-C显著降低(P<0·01),但大黄素组大鼠TG、TC和HDL-C可以得到纠正(P<0·01)。结论:大黄素可能通过纠正部分胃肠激素的异常表达提高2型糖尿病大鼠的胃动力。

关 键 词:大黄素  胃动力  2型糖尿病  大鼠  胃肠激素
文章编号:1001-0408(2008)15-1135-04
修稿时间:2007年6月10日

Mechanism of Effects of Emodin on Gastric Dynamics in Type 2 Diabetic Rats
LI Yan-fen,YAN Xiang,ZHAO Li,CHEN Ming,ZHANG Xin-hua.Mechanism of Effects of Emodin on Gastric Dynamics in Type 2 Diabetic Rats[J].China Pharmacy,2008,19(15):1135-1138.
Authors:LI Yan-fen  YAN Xiang  ZHAO Li  CHEN Ming  ZHANG Xin-hua
Affiliation:LI Yan-fen,YAN Xiang, ZHANG Xin-hua,ZHAO Li, CHEN Ming(Dept. of Gerontology, The First Hospital of Lanzhou University,Lanzhou 730000, China;Dept, of Nuclear Medicine, The First Hospital of Lanzhou University, Lanzhou 730000, China)
Abstract:OBJECTIVE: To investigate the mechanism of the effects of Emodin on the gastric motility of type 2 diabetic rats. METHODS: Murine type 2 diabetes model was induced in rats by intravenous injection of a small dose of streptozotocin plus long- term high fat high caloric laboratory chow. Then the model rats were treated with Emodin(EMO), tegaserod (TEG) or domperidone(DOM) for 6 weeks, with control(NOR) and model(MOD) groups as comparison. Gastric emptying half time(GET1/2) and 90 min residual rate(RIH) were measured by single photon emission computed tomography(SPECT) before sacrifice. The fasting blood glucose and serum insulin, riglycerides TG), total cholesterol(TC),high density lipoprotein cholesterol(HDL- C) were determined by biochemical methods. Plasma and tissue levels of substance P(SP) and somatostatin (SS) were determined using radioimmunoassay. RESULTS: Gastric emptying in model group was significantly slower than in normal control group(P 〈(0.01), but were significantly sped up after treatment by Emodin, tegaserod or domperidone(P 〈0.01 or P 〈0.05) . Plasma and intestine levels of SP were significantly increased while SS were significantly decreased after treatment by emodin, tegaserod or domperidone as compared with model group(P 〈 0.01 or P 〈 0.05). Serum TG and TC were significantly higher while HDL- C was lower in the model group and tegaserod or domperidone - treated group than those in normal group(P 〈0.01), but serum TG, TC and HDL- C levels were regulated to normal in Emodin- treated group(P 〈 0.01). CONCLUSION: Emodin can promote the gastrointestinal motility in type 2 diabetic rats is possibly related to its ability to regulate the abnormal expression of gastrointestinal hormones.
Keywords:Emodin  Gastric dynamics  Type 2 diabetic  Rats  Gut hormone
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