Suppr超能文献

抗精神病药物的受体结合谱。

Receptor-binding profiles of neuroleptics.

作者信息

Hyttel J, Larsen J J, Christensen A V, Arnt J

出版信息

Psychopharmacology Suppl. 1985;2:9-18. doi: 10.1007/978-3-642-70140-5_2.

Abstract

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.

摘要

多巴胺受体阻断似乎是抗精神病药物的一个显著作用。然而,阻断其他受体可能也有助于产生治疗效果。已对一系列抗精神病药物进行了测试,以检测它们对多巴胺D-1和D-2受体、5-羟色胺受体(S2)、α-肾上腺素能受体(α1)、组胺受体(H1)和毒蕈碱胆碱能受体的亲和力。根据对多巴胺D-1和D-2受体的亲和力,抗精神病药物可分为不同的组。噻吨类药物对D-1和D-2受体均有亲和力;吩噻嗪类药物对D-2受体有亲和力,而对D-1受体的亲和力则低得多;丁酰苯类、二苯基丁基哌啶类和苯甲酰胺类仅对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受体有亲和力。这些发现的临床意义具有推测性。在一些行为测试中也观察到了D-1/D-2分类,并且有人提出,D-1受体激活是导致运动障碍的原因,并且由于噻吨类药物具有D-1受体阻断作用,它们比其他抗精神病药物引起的运动障碍更少。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验