首都医科大学学报 ›› 2007, Vol. 28 ›› Issue (1): 75-77.

• 基础研究 • 上一篇    下一篇

自发性2型糖尿病小鼠发病早期认知功能的研究

王宪玲, 贾建平   

  1. 首都医科大学宣武医院神经内科
  • 收稿日期:2006-01-06 修回日期:1900-01-01 出版日期:2007-02-24 发布日期:2007-02-24

Study on the Cognition and the Pathogenetic Mechanisms of Early Stage in Diabetic KK-Ay Mouse

Wang Xianling, Jia Jianping   

  1. Department of Neurology, Xuanwu Hospital, Capital Medical University
  • Received:2006-01-06 Revised:1900-01-01 Online:2007-02-24 Published:2007-02-24

摘要: 目的 通过对自发性2型糖尿病小鼠发病早期认知功能的研究,探讨糖尿病脑病的发病机制。方法 利用自发性2型糖尿病动物模型KK-Ay小鼠,动态研究其认知功能的变化,并进行脑组织形态学观察。结果 在Morris水迷宫实验中,糖尿病小鼠在发病6周时已出现轻度认知功能障碍,在发病12周时认知功能障碍明显加重,游出时间、游出距离显著长于正常对照鼠(P<0.01)。光镜和电镜都观察到糖尿病小鼠脑组织形态学的变化,以电镜下超微结构的变化为主。发病12周时海马及颞叶神经元固缩、深染,核膜凹陷,核内染色质溶解,核糖体解聚,线粒体退变,内容物呈絮状,未观察到毛细血管基底膜增厚,管腔狭窄等血管病变。结论 KK-Ay小鼠可以作为研究糖尿病脑病的一种较好的动物模型;高血糖等代谢因素可引起认知障碍的发生。

关键词: 糖尿病脑病, 发病机制, KK-Ay糖尿病小鼠, 认知障碍

Abstract: Objective To study the pathogenic mechanisms of diabetic encephalopathy. Methods Using KK-Ay mouse as the non-insulin dependent diabetes mellitus(NIDDM) model and age-matched C57BL/6J mouse as normal control, their cognitive performance in Morris water maze and morphological change in brain has been observed respectively at 6 and 12 weeks after onset of diabetes mellitus. Results KK-Ay diabetic mouse begin to display moderate learning deficits in the Morris maze 6 weeks after onset of diabetes. The cognitive impairment become more significant at 12 weeks: the swimming time and distance of diabetic mouse is significantly longer than the control; the pathological change of brain tissue has been observed by electron microscopy and light microscopy. Conclusion KK-Ay diabetic mouse can be used as an animal model to study the pathogenesis of diabetic encephalopathy. The hyperglycemia may lead to the cognitive impairment in diabetes.

Key words: diabetic encephalopathy, pathogenetic mechanism, KK-Ay diabetic mouse, cognitive impairment

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