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胰岛素治疗高血压动脉硬化性脑梗死的实验研究 被引量:7

Effects of insulin on cerebral infarction in hypertensive and arteriosclerotic rats
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摘要 目的:观察胰岛素( Ins)对高血压动脉硬化大鼠脑梗死的疗效。方法:50 只肾血管性高血压大鼠( R H R)复制成大脑中动脉闭塞( M C Ao)模型,随机分4 组: A 组12 只( Ins 21 U/kg), B组12 只〔 Ins 21 U/kg+ 50% 葡萄糖(2 g/kg)〕, C组 12 只〔 Ins 45 U/kg+ 50% 葡萄糖(4 g/kg)〕和 D组 14 只(生理盐水 4 m l/kg)。各组均于 M C Ao 后即注射胰岛素, M C Ao 后 4 小时和24 小时检查神经功能,24 小时处死大鼠取脑,测大脑体积和梗死灶体积。结果: A 组的血糖较其他组有统计学意义的下降( P均< 001), C组的神经功能障碍评级、梗死灶体积及其与大脑体积的百分比的减少都有统计学意义( P 均< 001), A、 B、 D组间比较则无差异( P 均>005)。结论:胰岛素对缺血脑组织具有不依赖于其降糖作用的直接保护作用, R H R M C Ao 后注射胰岛素在较高剂量时才显示疗效,这可能与高血压致脑血管发生病变有关。 Objective:To observe the effects of insulin on cerebral infarction in hypertensive and arteriosclerotic rats.Methods:50 renovascular hypertensive rats (RHR) were subjected to middle cerebral artery occlusion (MCAo) and randomly allocated to four groups:group A ( n =12,insulin 2 1 U/kg),group B ( n =12,insulin 2 1 U/kg and 50% glucose 2 g/kg),group C( n =12,insulin 4 5 U/kg and 50% glucose 4 g/kg) and group D( n =14,normal saline 4 ml/kg).All rats were treated immediately following MCAo.Neurologic examinations were performed at 4 and 24 hours after MCAo in various groups.The rats surviving for 24 hours were killed to calculate cerebral volume and infarct volume.Results:The rats in group A had lower blood glucose levels than in group B,C,D(all P <0 01).The neurologic scores,total infarct volume and the percent of infarct volume in cerebral volume were significantly lower in group C than in the other groups and showed no significant differences among the other three groups.Conclusions:These results indicate that insulin exerts a direct protective effect on the ischemic brain independent of hypoglycemia.After MCAo,effects of high dose of insulin on RHR may be associated with cerebrovascular degeneration caused by hypertension.
出处 《中国危重病急救医学》 CAS CSCD 1999年第9期526-529,共4页 Chinese Critical Care Medicine
基金 广东省医药卫生青年科研基金
关键词 胰岛素 高血压 动脉硬化 大鼠 脑梗塞 治疗 insulin cerebral infarction hypertension arteriosclerosis rats CLC number:R977.15 R743.2 Document code:A Artical ID:10030603(1999)09052604
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