Drug Discovery Biology and Neuroscience & Mental Health Therapeutic Program Area, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
ARC Centre for Cryo-electron Microscopy of Membrane Proteins, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
Br J Pharmacol. 2024 Jul;181(14):2095-2113. doi: 10.1111/bph.16221. Epub 2023 Sep 26.
Schizophrenia remains a sizable socio-economic burden that continues to be treated with therapeutics based on 70-year old science. All currently approved therapeutics primarily target the dopamine D receptor to achieve their efficacy. Whilst dopaminergic dysregulation is a key feature in this disorder, the targeting of dopaminergic machinery has yielded limited efficacy and an appreciable side effect burden. Over the recent decades, numerous drugs that engage non-dopaminergic G protein-coupled receptors (GPCRs) have yielded a promise of efficacy without the deleterious side effect profile, yet none have successfully completed clinical studies and progressed to the market. More recently, there has been increased attention around non-dopaminergic GPCR-targeting drugs, which demonstrated efficacy in some schizophrenia symptom domains. This provides renewed hope that effective schizophrenia treatment may lie outside of the dopaminergic space. Despite the potential for muscarinic receptor- (and other well-characterised GPCR families) targeting drugs to treat schizophrenia, they are often plagued with complications such as lack of receptor subtype selectivity and peripheral on-target side effects. Orphan GPCR studies have opened a new avenue of exploration with many demonstrating schizophrenia-relevant mechanisms and a favourable expression profile, thus offering potential for novel drug development. This review discusses centrally expressed orphan GPCRs: GPR3, GPR6, GPR12, GPR52, GPR85, GPR88 and GPR139 and their relationship to schizophrenia. We review their expression, signalling mechanisms and cellular function, in conjunction with small molecule development and structural insights. We seek to provide a snapshot of the growing evidence and development potential of new classes of schizophrenia therapeutics. LINKED ARTICLES: This article is part of a themed issue Therapeutic Targeting of G Protein-Coupled Receptors: hot topics from the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists 2021 Virtual Annual Scientific Meeting. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.
精神分裂症仍然是一个相当大的社会经济负担,其治疗仍然基于 70 年前的科学。目前所有批准的治疗方法主要针对多巴胺 D 受体来实现疗效。虽然多巴胺能失调是这种疾病的一个关键特征,但多巴胺能机制的靶向治疗只产生了有限的疗效和相当大的副作用负担。在最近几十年,许多与非多巴胺能 G 蛋白偶联受体(GPCR)结合的药物显示出了疗效,而没有产生有害的副作用,但没有一种药物成功完成了临床研究并进入市场。最近,人们对非多巴胺能 GPCR 靶向药物越来越关注,这些药物在一些精神分裂症症状领域显示出了疗效。这为有效的精神分裂症治疗可能不在多巴胺能领域提供了新的希望。尽管毒蕈碱受体(和其他特征明确的 GPCR 家族)靶向药物治疗精神分裂症的潜力巨大,但它们常常受到缺乏受体亚型选择性和外周靶点副作用等并发症的困扰。孤儿 GPCR 研究开辟了新的探索途径,许多研究表明与精神分裂症相关的机制和有利的表达谱,因此为新药开发提供了潜力。本文讨论了中枢表达的孤儿 GPCR:GPR3、GPR6、GPR12、GPR52、GPR85、GPR88 和 GPR139 及其与精神分裂症的关系。我们综述了它们的表达、信号转导机制和细胞功能,以及小分子的开发和结构见解。我们试图提供一个新的视角,了解新一类精神分裂症治疗药物的不断发展的证据和开发潜力。相关文章:本文是治疗性靶向 G 蛋白偶联受体:2021 年澳大利亚临床和实验药理学与毒理学学会虚拟年会专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.html