α7烟碱受体激动剂:治疗精神分裂症和阿尔茨海默病认知障碍的潜在治疗药物

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2010-05-27 DOI:10.2174/1874104501004010037
Jun Toyohara, Kenji Hashimoto
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引用次数: 110

摘要

越来越多的证据表明,α7烟碱受体(α7 nAChRs)是nAChRs的一个亚型,在包括精神分裂症和阿尔茨海默病(AD)在内的神经精神疾病的病理生理中发挥作用。多项精神药理学和遗传学研究表明,α7 nAChR在精神分裂症患者P50听觉诱发电位缺陷中发挥重要作用,α nAChR激动剂有望成为治疗精神分裂症P50缺陷相关认知障碍的潜在药物。此外,一些研究表明α7 nAChR可能在淀粉样蛋白-β (a β)介导的AD病理中起关键作用,α7 nAChR激动剂可能是AD患者脑内a β沉积的潜在治疗药物。有趣的是,α7 nachr在精神分裂症和AD患者死后脑组织中的表达发生了改变。基于这些发现,选择性α7 nAChR激动剂可以被认为是治疗精神分裂症和AD认知障碍的潜在药物。在本文中,我们对α7 nAChR在这些疾病的病理生理中的作用以及新型α7 nAChR激动剂作为治疗药物的潜在应用进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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α7 Nicotinic Receptor Agonists: Potential Therapeutic Drugs for Treatment of Cognitive Impairments in Schizophrenia and Alzheimer's Disease.

Accumulating evidence suggests that α7 nicotinic receptors (α7 nAChRs), a subtype of nAChRs, play a role in the pathophysiology of neuropsychiatric diseases, including schizophrenia and Alzheimer's disease (AD). A number of psychopharmacological and genetic studies shown that α7 nAChRs play an important role in the deficits of P50 auditory evoked potential in patients with schizophrenia, and that (α nAChR agonists would be potential therapeutic drugs for cognitive impairments associated with P50 deficits in schizophrenia. Furthermore, some studies have demonstrated that α7 nAChRs might play a key role in the amyloid-β (Aβ)-mediated pathology of AD, and that α7 nAChR agonists would be potential therapeutic drugs for Aβ deposition in the brains of patients with AD. Interestingly, the altered expression of α7 nAChRs in the postmortem brain tissues from patients with schizophrenia and AD has been reported. Based on all these findings, selective α7 nAChR agonists can be considered potential therapeutic drugs for cognitive impairments in both schizophrenia and AD. In this article, we review the recent research into the role of α7 nAChRs in the pathophysiology of these diseases and into the potential use of novel α7 nAChR agonists as therapeutic drugs.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
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0.00%
发文量
4
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