Schmidt C J, Sorensen S M, Kehne J H, Carr A A, Palfreyman M G
Marion Merrell Dow Research Institute, Cincinnati, Ohio 45215, USA.
Life Sci. 1995;56(25):2209-22. doi: 10.1016/0024-3205(95)00210-w.
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.
抗精神病药物的临床活性与其对D2多巴胺受体的亲和力之间的相关性,一直是精神分裂症是由于多巴胺能功能亢进这一假说的支柱。最近,有人提出非典型抗精神病药物氯氮平独特的临床特征涉及对其他受体系统的作用。特别是,氯氮平对5HT2A受体亚型的高亲和力被认为有助于其降低副作用风险、提高疗效以及在难治性精神分裂症中的活性。我们使用了高度选择性的5-HT2A拮抗剂MDL 100,907来探讨5-HT2A受体阻断对抗精神病活性的贡献。生化、电生理和行为学研究表明,选择性5HT2A受体拮抗剂具有非典型抗精神病药物的临床前特征。现有的有限临床证据也表明,产生5-HT2A受体阻断作用的化合物是有效的,特别是对精神分裂症的阴性症状有效。