摘要
目的:在具有胰岛素抵抗特征近似人类2型糖尿病(T2DM)的大鼠身上建立脑梗死模型。方法:SD雄性大鼠120只,其中90只用高脂高糖和链脲佐菌素(STZ)制成T2DM模型,另30只为对照组。对照组和T2DM成模大鼠随机分为假手术组(A1组、B1组)和手术组(A2组、B2组)。采用神经功能缺损量表(NSS)评分、TTC染色与HE染色观察神经功能缺损征、脑梗死体积及病理改变。结果:T2DM成模率为72%,血脂指标与对照组相比差异有统计学意义(P〈0.01),且血脂异常表现与临床T2DM患者近似。A2组NSS评分3—4级者占75%,脑梗死体积为(55.23±9.59)mm^3,脑梗死成模率为75%;B2组NSS评分3—4级者占60%,脑梗死体积为(54.33±6.39)mm^3,脑梗死成模率为53%。结论:高脂膳食结合STZ注射能复制出接近人类T2DM的动物模型,在此基础上制成的脑梗死模型稳定性和重复性好,是研究人类糖尿病脑梗死病理过程较为理想的动物模型。
Objective:To establish an animal model similar to the metabolic abnormality of human Type 2 diabetes mellitus(T2DM) with insulin resistance and cerebral infarction (CI). Methods: SD male rats(n=120) were divided into the model group(T2DM,90) induced by high-fatty diet and injection of streptozotocin(STZ)and the control group(30). Ninety of whom were fed high-fatty diet and STZ. Controls were randomly divided into A1 (sham-operated, 5) and A2 (operated, 5)and models were B1 (sham-operated,15 ) and B2 (operated,15). Neurological severity score (NSS) , triphenyl tetrazolium chloride (TTC) staining and HE staining were adopted to observe dynamically the syndrome of neurological severity, the volume of CI and the pathological changes. Results: The successful rate of T2DM execution was 76% whose LDL, TC, TG were different compared with controls (P〈0. 01)and similar to clinical Type 2 diabetes mellitus. In the model A2, the successful rates of execution was 75%,3-4 grade of neurological deficit scoring 75%and the volume of CI(55.23±9.59)mm3 respectively. In the model B2,the successful rate of execution was 53.3% 3-4 grade of neurological deficit scoring 60%and volume of CI (54.33±6.39)mm3 respectively. The sham group A1 and B1 behavior change normal at 24 h. Conclusion: Type 2 diabetes mellitus animal model is successfully reproduced by using the high fatty diet plus STZ injection. CI rat models with ischemia-reperfusion were stable and repeatable and provide a perfect animal model for investigating pharmacology of diabetes mellitus.
出处
《临床神经电生理学杂志》
2009年第5期270-274,共5页
Journal of Clinical Electroneurophysiology
基金
云南省科技厅-昆明医学院联合专项基金资助(No:2007C139M),昆明医学院博士创新基金项目(No:KM2007D02)