Gray John A, Roth Bryan L
Department of Psychiatry, University of California, San Fransico, CA, USA.
Schizophr Bull. 2007 Sep;33(5):1100-19. doi: 10.1093/schbul/sbm074. Epub 2007 Jul 7.
Cognitive impairment is a core feature of schizophrenia as deficits are present in the majority of patients, frequently precede the onset of other positive symptoms, persist even with successful treatment of positive symptoms, and account for a significant portion of functional impairment in schizophrenia. While the atypical antipsychotics have produced incremental improvements in the cognitive function of patients with schizophrenia, overall treatment remains inadequate. In recent years, there has been an increased interest in developing novel strategies for treating the cognitive deficits in schizophrenia, focusing on ameliorating impairments in working memory, attention, and social cognition. Here we review various molecular targets that are actively being explored for potential drug discovery efforts in schizophrenia and cognition. These molecular targets include dopamine receptors in the prefrontal cortex, nicotinic and muscarinic acetylcholine receptors, the glutamatergic excitatory synapse, various serotonin receptors, and the gamma-aminobutyric acid (GABA) system.
认知障碍是精神分裂症的核心特征,因为大多数患者都存在认知缺陷,这些缺陷常常先于其他阳性症状出现,即使阳性症状得到成功治疗仍会持续存在,并且在精神分裂症的功能障碍中占很大比例。虽然非典型抗精神病药物已使精神分裂症患者的认知功能有了逐步改善,但总体治疗仍不充分。近年来,人们对开发治疗精神分裂症认知缺陷的新策略越来越感兴趣,重点是改善工作记忆、注意力和社会认知方面的障碍。在此,我们综述了目前正在积极探索的各种分子靶点,这些靶点有望用于精神分裂症和认知方面的潜在药物研发。这些分子靶点包括前额叶皮质中的多巴胺受体、烟碱型和毒蕈碱型乙酰胆碱受体、谷氨酸能兴奋性突触、各种5-羟色胺受体以及γ-氨基丁酸(GABA)系统。