Department of Pharmacology and Hugh Green Biobank, Centre for Brain Research, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
Trends Pharmacol Sci. 2020 Nov;41(11):777-792. doi: 10.1016/j.tips.2020.09.002. Epub 2020 Sep 28.
Central nervous system (CNS) drug development has been plagued by a failure to translate effective therapies from the lab to the clinic. There are many potential reasons for this, including poor understanding of brain pharmacokinetic (PK) and pharmacodynamic (PD) factors, preclinical study flaws, clinical trial design issues, the complexity and variability of human brain diseases, as well as species differences. To address some of these problems, we have developed a platform for CNS drug discovery comprising: drug screening of primary adult human brain cells; human brain tissue microarray analysis of drug targets; and high-content phenotypic screening methods. In this opinion, I summarise the theoretical basis and the practical development and use of this platform in CNS drug discovery.
中枢神经系统(CNS)药物开发一直受到未能将有效的治疗方法从实验室转化为临床的困扰。造成这种情况的原因有很多,包括对脑药代动力学(PK)和药效学(PD)因素的了解不足、临床前研究缺陷、临床试验设计问题、人脑疾病的复杂性和变异性,以及物种差异。为了解决其中的一些问题,我们开发了一个包含以下内容的中枢神经系统药物发现平台:对原代成年人大脑细胞进行药物筛选;药物靶点的人脑组织微阵列分析;以及高内涵表型筛选方法。在这篇观点文章中,我总结了该平台在中枢神经系统药物发现中的理论基础和实际开发及应用。