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精神药物对人外周和中枢毒蕈碱型胆碱能受体亲和力的比较。

A comparison of peripheral and central human muscarinic cholinergic receptor affinities for psychotropic drugs.

作者信息

Tollefson G D, Senogles S E, Frey W H, Tuason V B, Nicol S E

出版信息

Biol Psychiatry. 1982 May;17(5):555-67.

PMID:7093392
Abstract

A peripheral model offers a valuable research tool for the investigation of central cholinopathic disorders. The in vitro affinities of several psychotropic drugs for the muscarinic cholinergic binding sites of human caudate and erythrocyte were compared in competition with a tritiated antagonist (quinuclidinyl benzilate). The relative affinities of the drugs for both tissues were strikingly similar. Thus, the erythrocyte muscarinic receptor may represent an accessible in vitro assay for the characterization of central cholinopathic states.

摘要

外周模型为研究中枢胆碱能病变提供了一种有价值的研究工具。通过与一种氚标记的拮抗剂(喹核醇苯酸酯)竞争,比较了几种精神药物对人尾状核和红细胞毒蕈碱胆碱能结合位点的体外亲和力。这些药物对两种组织的相对亲和力惊人地相似。因此,红细胞毒蕈碱受体可能代表了一种可用于表征中枢胆碱能病变状态的体外检测方法。

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