Girgis R R, Javitch J A, Lieberman J A
Department of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Mol Psychiatry. 2008 Oct;13(10):918-29. doi: 10.1038/mp.2008.40. Epub 2008 Apr 15.
The exact therapeutic mechanism of action of antipsychotic drugs remains unclear. Recent evidence has shown that second-generation antipsychotic drugs (SGAs) are differentially associated with metabolic side effects compared to first-generation antipsychotic drugs (FGAs). Their proclivity to cause metabolic disturbances correlates, to some degree, with their comparative efficacy. This is particularly the case for clozapine and olanzapine. In addition, the insulin signaling pathway is vital for normal brain development and function. Abnormalities of this pathway have been found in persons with schizophrenia and antipsychotic drugs may ameliorate some of these alterations. This prompted us to hypothesize that the therapeutic antipsychotic and adverse metabolic effects of antipsychotic drugs might be related to a common pharmacologic mechanism. This article reviews insulin metabolism in the brain and related abnormalities associated with schizophrenia with the goals of gaining insight into antipsychotic drug effects and possibly also into the pathophysiology of schizophrenia. Finally, we speculate about one potential mechanism of action (that is, functional selectivity) that would be consistent with the data reviewed herein and make suggestions for the future investigation that is required before a therapeutic agent based on these data can be realized.
抗精神病药物的确切治疗作用机制尚不清楚。最近的证据表明,与第一代抗精神病药物(FGAs)相比,第二代抗精神病药物(SGAs)与代谢副作用的关联存在差异。它们导致代谢紊乱的倾向在一定程度上与其相对疗效相关。氯氮平和奥氮平尤其如此。此外,胰岛素信号通路对正常大脑发育和功能至关重要。在精神分裂症患者中发现了该通路的异常,抗精神病药物可能会改善其中一些改变。这促使我们推测,抗精神病药物的治疗性抗精神病作用和不良代谢作用可能与一种共同的药理机制有关。本文综述了大脑中的胰岛素代谢以及与精神分裂症相关的异常情况,目的是深入了解抗精神病药物的作用,也可能深入了解精神分裂症的病理生理学。最后,我们推测了一种与本文所综述的数据一致的潜在作用机制(即功能选择性),并对在基于这些数据的治疗药物实现之前所需的未来研究提出了建议。