Nair Pramod C, McKinnon Ross A, Miners John O, Bastiampillai Tarun
Department of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Adelaide, SA, Australia.
Flinders Centre for Innovation in Cancer, College of Medicine and Public Health, Flinders University, Adelaide, SA, Australia.
Mol Psychiatry. 2020 Sep;25(9):1910-1919. doi: 10.1038/s41380-020-0709-5. Epub 2020 Mar 13.
Clozapine is the gold-standard agent for treatment resistant schizophrenia but its mechanism of action remains unclear. There is emerging evidence of the potential role of the GABA receptor in the pathogenesis of schizophrenia. It has been hypothesised that clozapine can mediate its actions via the GABA receptor. Baclofen is currently recognised as the prototype GABA receptor agonist. There are some potential clinical similarities between clozapine and baclofen. Indeed, baclofen has been previously proposed for use as an antipsychotic agent. Our analysis of the X-ray crystal structure of GABA receptor along with molecular docking calculations, suggests that clozapine could directly bind to the GABA receptor similar to that of baclofen. This finding could lead to a better understanding of the pharmacological uniqueness of clozapine, potential development of a biomarker for treatment resistant schizophrenia and the development of more targeted treatments leading to personalisation of treatment.
氯氮平是治疗难治性精神分裂症的金标准药物,但其作用机制仍不清楚。越来越多的证据表明γ-氨基丁酸(GABA)受体在精神分裂症发病机制中具有潜在作用。有假说认为氯氮平可通过GABA受体介导其作用。巴氯芬目前被认为是GABA受体激动剂的原型。氯氮平和巴氯芬之间存在一些潜在的临床相似之处。事实上,巴氯芬此前曾被提议用作抗精神病药物。我们对GABA受体的X射线晶体结构进行分析,并结合分子对接计算,结果表明氯氮平可能与巴氯芬类似,直接与GABA受体结合。这一发现可能有助于更好地理解氯氮平的药理学独特性,为难治性精神分裂症开发潜在的生物标志物,并开发更具针对性的治疗方法,实现个性化治疗。