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硫胺素焦磷酸治疗大鼠大脑中毒蕈碱型胆碱能受体亚型的定量放射自显影研究。

A quantitative autoradiographic study of muscarinic cholinergic receptor subtypes in the brains of pyrithiamine-treated rats.

作者信息

Rao V L, Mousseau D D, Butterworth R F

机构信息

Neuroscience Research Unit, Hôpital Saint-Luc, University of Montreal, QC, Canada.

出版信息

Neurochem Res. 1995 Aug;20(8):907-14. doi: 10.1007/BF00970736.

Abstract

Previous studies describe decreased acetylcholine synthesis in brain as well as neurobehavioral evidence for a central muscarinic cholinergic deficit in pyrithiamine-induced thiamine-deficient rats. In order to further evaluate this possibility, quantitative autoradiographic procedures using [3H]quinuclidinyl benzilate (for total muscarinic binding sites), [3H]pirenzepine (for muscarinic M1 sites) and [3H]AF-DX 384 (for muscarinic M2 sites) were performed at early (presymptomatic) and late (symptomatic) stages of thiamine deficiency induced in rats by administration of the central thiamine antagonist, pyrithiamine. No significant alterations in densities of M1, M2 or total muscarinic binding sites were observed in any brain structure evaluated at either early or late stages of thiamine deficiency. These findings do not support a major role for modifications of muscarinic cholinergic function in the pathogenesis of the neurological symptoms of thiamine deficiency.

摘要

先前的研究描述了脑内乙酰胆碱合成减少,以及硫胺素缺乏诱导的大鼠中,中枢毒蕈碱胆碱能缺陷的神经行为学证据。为了进一步评估这种可能性,在给大鼠施用中枢硫胺素拮抗剂吡硫胺素诱导硫胺素缺乏的早期(症状前)和晚期(有症状)阶段,使用[3H]喹核醇基苯甲酸酯(用于总毒蕈碱结合位点)、[3H]哌仑西平(用于毒蕈碱M1位点)和[3H]AF-DX 384(用于毒蕈碱M2位点)进行了定量放射自显影程序。在硫胺素缺乏的早期或晚期评估的任何脑结构中,均未观察到M1、M2或总毒蕈碱结合位点密度的显著改变。这些发现不支持毒蕈碱胆碱能功能改变在硫胺素缺乏神经症状发病机制中的主要作用。

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