受体
氯氮平
氯丙嗪
药理学
非定型抗精神病薬
抗精神病药
抗精神病药
化学
亲缘关系
抗精神病薬
多巴胺受体D2
5-羟色胺受体
5-HT2受体
浣熊
血清素
血清素拮抗剂
生物
生物化学
医学
精神分裂症(面向对象编程)
精神科
作者
Deleted Author ID,S Craigo,M S Choudhary,Ahmet Uluer,Frederick J. Monsma,Yihui Shen,Herbert Y. Meltzer,David R. Sibley
出处
期刊:PubMed
[National Institutes of Health]
日期:2018-11-07
卷期号:268 (3): 1403-10
被引量:223
摘要
The authors examined the affinities of 36 typical and atypical antipsychotic agents for the cloned rat 5-hydroxytryptamine-6 (5-HT6) and rat 5-hydroxytryptamine-7 (5-HT7) receptors in transiently expressed COS-7 cells (5-HT7) or stably transfected HEK-293 cells (5-HT6 receptors). Clozapine and several related atypical antipsychotic agents (rilapine, olanzepine, tiospirone, fluperlapine, clorotepine and zotepine) had high affinities for the newly discovered 5-HT6 receptor (Kis < 20 nM). The 5-HT7 receptor bound clozapine, rilapine, fluperlapine, clorotepine, zotepine and risperidone but not tiospirone and olanzepine, with affinities less than 15 nM. In addition, several typical antipsychotic agents (chloroprothixene, chlorpromazine, clothiapine and fluphenazine) had high affinities for both the 5-HT6 and 5-HT7 receptors. Pimozide, a diphenylbutylpiperidine, had the highest affinity of all the typical antipsychotic agents tested for the 5-HT7 receptor (Ki = 0.5 nM). Three putative atypical antipsychotic agents melperone, amperozide and MDL 100907 did not bind with high affinities to either the 5-HT6 or 5-HT7 receptors (Kis > 50 nM). Several dopamine-selective antipsychotic agents (raclopride, rimcazole and penfluridol) had essentially no affinity for either the 5-HT6 or 5-HT7 receptors (Ki values > 5000 nM).(ABSTRACT TRUNCATED AT 250 WORDS)
科研通智能强力驱动
Strongly Powered by AbleSci AI