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褪黑素对早期糖尿病大鼠心肌非酶糖基化及氧化应激反应的影响
引用本文:李青菊,姚蔚,李凤良,李鹏诺,张苏河. 褪黑素对早期糖尿病大鼠心肌非酶糖基化及氧化应激反应的影响[J]. 郑州大学学报(医学版), 2005, 40(3): 489-490
作者姓名:李青菊  姚蔚  李凤良  李鹏诺  张苏河
作者单位:郑州大学第二附属医院内分泌科,郑州,450014;郑州大学第二附属医院内分泌科,郑州,450014;郑州大学第二附属医院内分泌科,郑州,450014;郑州大学第二附属医院内分泌科,郑州,450014;郑州大学第二附属医院内分泌科,郑州,450014
摘    要:目的:研究褪黑素(Mel)对糖尿病大鼠氧化应激反应和非酶糖基化反应的影响。方法:用链脲佐菌素腹腔注射制备糖尿病大鼠模型。正常大鼠、糖尿病大鼠及用褪黑素治疗8周的糖尿病大鼠各10只,应用荧光法测定心肌组织糖基化终末产物(AGEs)含量,应用比色法测定心肌组织及血清丙二醛(MDA)含量,乳胶免疫聚集抑制法测定糖化血红蛋白(HbA1c)含量,计算心脏质量指数。结果:与正常大鼠比较,糖尿病大鼠各指标升高,而褪黑素组血清MDA以及心肌组织中AGEs、MDA含量和心脏质量指数均较糖尿病组下降。结论:褪黑素能抑制糖尿病大鼠心肌非酶糖基化和氧化应激反应。

关 键 词:糖尿病  心肌病  褪黑素  非酶糖基化  氧化应激反应  大鼠
修稿时间:2004-10-11

Effect of melatonin on nonenzymaticglycation and oxidation stress in myocardial tissue of diabetic rats
LI Qingju,YAO Wei,LI Fengliang,LI Pengnuo,ZHANG Suhe. Effect of melatonin on nonenzymaticglycation and oxidation stress in myocardial tissue of diabetic rats[J]. Journal of Zhengzhou University: Med Sci, 2005, 40(3): 489-490
Authors:LI Qingju  YAO Wei  LI Fengliang  LI Pengnuo  ZHANG Suhe
Affiliation:LI Qingju,YAO Wei,LI Fengliang,LI Pengnuo,ZHANG Suhe Department of Endocrinology,the Second Affiliated Hospital,Zhengzhou University,Zhengzhou 450014
Abstract:Aim: To investigate the effects of melatonin on nonenzymaticglycation and oxidative stress in diabetic rats.Methods: The subjects were 10 normal rats,10 diabetic rats,and 10 diabetic rats treated with Melatonin(Mel) per day for 8 weeks.The fluorescence assay was used to determine the levels of AGEs.The colorimetry was used to determine the levels of MDA from myocardial tissue and serum, respectively. Results: In the diabetic rats, HbA1c in serum, AGEs and MDA in myocytes and the ratio of heart to weight were significantly higher than those in normal controls. After being treated with Mel, serum MDA, AGEs and myocytes MDA and the ratio of heart to weight were significantly decreased than those in diabetic group. Conclusion: Mel inhibits both nonenzymaticglycation and oxidative stress in heart of diabetic rats.
Keywords:diabetes  cardiomyopathy  melatonin  nonenzymaticglycation  oxidative stress  rat
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