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多巴胺、认知障碍与第二代抗精神病药物:从机制进展到更个性化的治疗

Dopamine, Cognitive Impairments and Second-Generation Antipsychotics: From Mechanistic Advances to More Personalized Treatments.

作者信息

Torrisi Sebastiano Alfio, Laudani Samuele, Contarini Gabriella, De Luca Angelina, Geraci Federica, Managò Francesca, Papaleo Francesco, Salomone Salvatore, Drago Filippo, Leggio Gian Marco

机构信息

Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy.

Genetics of Cognition laboratory, Neuroscience area, Istituto Italiano di Tecnologia, 16163 Genova, Italy.

出版信息

Pharmaceuticals (Basel). 2020 Nov 5;13(11):365. doi: 10.3390/ph13110365.

Abstract

The pharmacological treatment of cognitive impairments associated with schizophrenia is still a major unmet clinical need. Indeed, treatments with available antipsychotics generate highly variable cognitive responses among patients with schizophrenia. This has led to the general assumption that antipsychotics are ineffective on cognitive impairment, although personalized medicine and drug repurposing approaches might scale down this clinical issue. In this scenario, evidence suggests that cognitive improvement exerted by old and new atypical antipsychotics depends on dopaminergic mechanisms. Moreover, the newer antipsychotics brexpiprazole and cariprazine, which might have superior clinical efficacy on cognitive deficits over older antipsychotics, mainly target dopamine receptors. It is thus reasonable to assume that despite more than 50 years of elusive efforts to develop novel non-dopaminergic antipsychotics, dopamine receptors remain the most attractive and promising pharmacological targets in this field. In the present review, we discuss preclinical and clinical findings showing dopaminergic mechanisms as key players in the cognitive improvement induced by both atypical antipsychotics and potential antipsychotics. We also emphasize the concept that these mechanistic advances, which help to understand the heterogeneity of cognitive responses to antipsychotics, may properly guide treatment decisions and address the unmet medical need for the management of cognitive impairment associated with schizophrenia.

摘要

精神分裂症相关认知障碍的药物治疗仍是一项尚未满足的重大临床需求。事实上,使用现有抗精神病药物进行治疗时,精神分裂症患者的认知反应差异很大。这导致人们普遍认为抗精神病药物对认知障碍无效,尽管个性化医疗和药物重新利用方法可能会减少这一临床问题。在这种情况下,有证据表明,新旧非典型抗精神病药物所带来的认知改善取决于多巴胺能机制。此外,新型抗精神病药物布瑞哌唑和卡立哌嗪可能比旧型抗精神病药物在认知缺陷方面具有更高的临床疗效,它们主要作用于多巴胺受体。因此,尽管在开发新型非多巴胺能抗精神病药物方面经过了50多年的不懈努力,但多巴胺受体仍然是该领域最具吸引力和前景的药理学靶点,这一假设是合理的。在本综述中,我们讨论了临床前和临床研究结果,这些结果表明多巴胺能机制在非典型抗精神病药物和潜在抗精神病药物诱导的认知改善中起着关键作用。我们还强调了这样一个概念,即这些机制方面的进展有助于理解对抗精神病药物认知反应的异质性,可能会恰当地指导治疗决策,并满足精神分裂症相关认知障碍管理方面未得到满足的医疗需求。

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