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Antipsychotic drug mechanisms: links between therapeutic effects, metabolic side effects and the insulin signaling pathway

机译:抗精神病药物机制:治疗作用,代谢副作用与胰岛素信号传导途径之间的联系

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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.
机译:抗精神病药的确切治疗作用机理尚不清楚。最近的证据表明,与第一代抗精神病药物(FGA)相比,第二代抗精神病药物(SGA)与代谢副作用存在差异。它们引起代谢紊乱的倾向在一定程度上与其比较功效相关。氯氮平和奥氮平尤其如此。此外,胰岛素信号通路对于正常的大脑发育和功能至关重要。在精神分裂症患者中发现了该途径的异常,抗精神病药可能会缓解其中的某些改变。这促使我们假设抗精神病药的治疗性抗精神病药和不良代谢作用可能与常见的药理机制有关。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,旨在深入了解抗精神病药物的作用,并可能进一步了解精神分裂症的病理生理学。最后,我们推测了一种潜在的作用机制(即功能选择性),该机制将与本文中回顾的数据保持一致,并为实现基于这些数据的治疗剂所需的未来研究提供建议。

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