抗精神病药的受体结合谱。

J Hyttel, J J Larsen, A V Christensen, J Arnt
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引用次数: 133

摘要

多巴胺受体阻断似乎是抗精神病药的显著作用。然而,阻断其他受体可能有助于治疗效果。一系列的神经阻滞剂已被测试对DA -1和D-2受体、5 -羟色胺受体(S2)、α -肾上腺素受体(α 1)、组胺受体(H1)和毒蕈碱胆碱能受体的亲和力。根据对DA D-1和D-2受体的亲和力,可将抗精神病药分为不同的类群。硫代蒽对D-1和D-2受体都有亲和力;吩噻嗪类药物对D-2受体有亲和力,对D-1受体的亲和力较低;而丁苯酮类、二苯基丁基哌啶类和苯酰胺类仅对D-2受体有亲和力。关于对其他受体的亲和力,唯一一致的发现是对S2受体的亲和力。这些发现的临床意义是推测性的。在一些行为测试中也观察到D-1/D-2的分类,并且表明D-1受体的激活是导致运动障碍的原因,而噻吩类-由于其D-1受体阻断作用-比其他抗精神病药诱导的运动障碍更少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Receptor-binding profiles of neuroleptics.

Dopamine-receptor blockade seems to be a prominent effect of neuroleptics. Blockade of other receptors might, however, contribute to the therapeutic effect. A series of neuroleptics have been tested for affinity to DA D-1 and D-2 receptors, serotonin receptors (S2), alpha-adrenoceptors (alpha 1), histamine receptors (H1), and muscarinic cholinergic receptors. According to the affinity to DA D-1 and D-2 receptors, neuroleptics can be divided into different groups. Thioxanthenes have affinity for both D-1 and D-2 receptors; phenothiazines have affinity for D-2 receptors and considerably lower affinity for D-1 receptors; and butyrophenones, diphenylbutylpiperidines, and benzamides have affinity only for D-2 receptors. Concerning affinity to other receptors the only consistent finding is affinity for S2 receptors. The clinical significance of these findings is speculative. In several behavioral tests the D-1/D-2 classification is also observed, and it is suggested that D-1-receptor activation is responsible for dyskinesia, and that thioxanthenes - due to their D-1 receptor blocking effect-induce less dyskinesia than other neuroleptics.

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