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纹状体中胆碱能受体表达降低:低血糖和糖尿病大鼠的运动功能缺陷。

Decreased cholinergic receptor expression in the striatum: motor function deficit in hypoglycemic and diabetic rats.

机构信息

Department of Biotechnology, Cochin University of Science and Technology, Cochin, 682 022, Kerala, India.

出版信息

Cell Mol Neurobiol. 2012 Jan;32(1):83-93. doi: 10.1007/s10571-011-9738-6. Epub 2011 Jul 28.

Abstract

Hypoglycemic brain injury is a common and serious complication of insulin therapy associated with diabetes. This study evaluated the effect of insulin-induced hypoglycemia and STZ-induced diabetes on striatal cholinergic receptors and enzyme expression and on motor function. Cholinergic enzymes: AChE and ChAT gene expression, radioreceptor binding assay and immunohistochemistry of muscarinic M1, M3 receptors and α7nAChR were carried out. Motor performance on grid walk test was analysed. AChE and ChAT expression significantly downregulated in hypoglycemic and diabetic rats. Total muscarinic and Muscarinic M3 receptor binding decreased in hypoglycemic rats compared to diabetic rats whereas muscarinic M1 receptor binding increased in hypoglycemic rats compared to diabetic rats. Real-time PCR analysis and confocal imaging of muscarinic M1, M3 receptors confirmed the changes in muscarinic receptor binding in hypoglycemic and diabetic rats. In hypoglycemic rats, α7nAChR expression significantly up regulated compared to diabetic rats. Grid walk test demonstrated the impairment in motor function and coordination in hypoglycemic and hyperglycemic rats. Neurochemical changes along with the behavioral data implicate a role for impaired striatal cholinergic receptor function inducing motor function deficit induced by hypo and hyperglycemia. Hypoglycemia exacerbated the neurobehavioral deficit in diabetes which has clinical significance in the treatment of diabetes.

摘要

低血糖性脑损伤是糖尿病患者胰岛素治疗相关的一种常见且严重的并发症。本研究评估了胰岛素诱导的低血糖和 STZ 诱导的糖尿病对纹状体胆碱能受体和酶表达以及运动功能的影响。进行了胆碱能酶:AChE 和 ChAT 基因表达、放射受体结合测定和毒蕈碱 M1、M3 受体和α7nAChR 的免疫组织化学分析。通过网格行走测试分析运动性能。与糖尿病大鼠相比,低血糖大鼠的 AChE 和 ChAT 表达显著下调。与糖尿病大鼠相比,低血糖大鼠的总毒蕈碱和毒蕈碱 M3 受体结合减少,而低血糖大鼠的毒蕈碱 M1 受体结合增加。毒蕈碱 M1、M3 受体的实时 PCR 分析和共聚焦成像证实了低血糖和糖尿病大鼠毒蕈碱受体结合的变化。与糖尿病大鼠相比,低血糖大鼠的α7nAChR 表达显著上调。网格行走测试表明,低血糖和高血糖大鼠的运动功能和协调性受损。神经化学变化以及行为数据表明,纹状体胆碱能受体功能受损导致低血糖和高血糖引起的运动功能缺陷。低血糖使糖尿病的神经行为缺陷恶化,这在糖尿病的治疗中具有临床意义。

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