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本文引用的文献

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Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand.改造锁以适配钥匙,从而创建出一族能被惰性配体有效激活的G蛋白偶联受体。
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A 12-week, double-blind, placebo-controlled trial of galantamine adjunctive treatment to conventional antipsychotics for the cognitive impairments in chronic schizophrenia.一项为期12周的双盲、安慰剂对照试验,评估加兰他敏辅助传统抗精神病药物治疗慢性精神分裂症认知障碍的效果。
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Phosphodiesterase 10A inhibitors: a novel approach to the treatment of the symptoms of schizophrenia.磷酸二酯酶10A抑制剂:一种治疗精神分裂症症状的新方法。
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Towards a muscarinic hypothesis of schizophrenia.迈向精神分裂症的毒蕈碱假说。
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Cognitive dysfunctions in schizophrenia: potential benefits of cholinesterase inhibitor adjunctive therapy.精神分裂症中的认知功能障碍:胆碱酯酶抑制剂辅助治疗的潜在益处。
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COMT val108/158met genotype, cognitive function, and cognitive improvement with clozapine in schizophrenia.儿茶酚-O-甲基转移酶(COMT)val108/158met基因型、认知功能以及氯氮平对精神分裂症认知功能的改善作用
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Acute effects of the ampakine farampator on memory and information processing in healthy elderly volunteers.安帕金farampator对健康老年志愿者记忆和信息处理的急性影响。
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Glycogen synthase kinase-3 (GSK3) in psychiatric diseases and therapeutic interventions.糖原合酶激酶-3(GSK3)在精神疾病及治疗干预中的作用
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治疗精神分裂症认知功能障碍的分子靶点。

Molecular targets for treating cognitive dysfunction in schizophrenia.

作者信息

Gray John A, Roth Bryan L

机构信息

Department of Psychiatry, University of California, San Fransico, CA, USA.

出版信息

Schizophr Bull. 2007 Sep;33(5):1100-19. doi: 10.1093/schbul/sbm074. Epub 2007 Jul 7.

DOI:10.1093/schbul/sbm074
PMID:17617664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2632344/
Abstract

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.

摘要

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。