5-HT2A受体
抗精神病药
氯氮平
多巴胺受体D2
精神分裂症(面向对象编程)
非定型抗精神病薬
抗精神病药
抗精神病薬
药理学
多巴胺能
多巴胺受体D3
封锁
受体
心理学
神经科学
医学
5-羟色胺受体
多巴胺
内科学
血清素
精神科
作者
Christopher J. Schmidt,Stephen M. Sorensen,John H. Kehne,Albert A. Carr,Michael G. Palfreyman
出处
期刊:Life Sciences
[Elsevier BV]
日期:1995-05-01
卷期号:56 (25): 2209-2222
被引量:198
标识
DOI:10.1016/0024-3205(95)00210-w
摘要
The correlation between the clinical activity of antipsychotic agents and their affinity for the D2 dopamine receptor has been the mainstay of the hypothesis that schizophrenia is due to excessive dopaminergic function. More recently, the unique clinical profile of the atypical antipsychotic clozapine has been proposed to involve actions on additional receptor systems. In particular, the high affinity of clozapine for the 5HT2A receptor subtype has been suggested to contribute to its reduced side-effect liability, greater efficacy and its activity in therapy-resistant schizophrenia. We have used the highly selective 5-HT2A antagonist MDL 100,907 to explore the contribution of 5-HT2A receptor blockade to antipsychotic activity. Biochemical, electrophysiological and behavioral studies reveal that selective 5HT2A receptor antagonists have the preclinical profile of an atypical antipsychotic. The limited clinical evidence available also suggests that compounds producing 5-HT2A receptor blockade are effective, in particular, against the negative symptoms of schizophrenia.
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