Cognitive Translational Behavioural Pharmacology Group, Department of Pharmacology and Pharmacotherapy, Semmelweis University , Budapest, Hungary.
Expert Opin Drug Discov. 2020 Jun;15(6):659-670. doi: 10.1080/17460441.2020.1739645. Epub 2020 Mar 18.
Disorders of the brain pose the biggest health challenge of this century with new and highly efficacious medications urgently needed. This article discusses the challenges of meeting this increasing demand by neuropsychiatric drug discovery.
The current psychopharmacological armamentarium relies on targets discovered several decades ago. Moreover, a major part of the current pipeline of potential cognitive enhancers also contains compounds with multiple failed modes of action which had not been properly validated before the clinic. Further, the feasibility limits of preventive pharmacology should also be taken into account. Advancements in neuroimaging and genetic studies have highlighted epigenetic regulation and synaptic plasticity as potential 'hot points' for pharmacological interventions in neuropsychiatric disorders. However, in the meantime new, rapidly evolving technologies have given rise to alternative treatment options such as brain stimulation, cell and gene therapy.
Neuropsychiatric drug discovery should turn toward non-neurotransmitter-related targets such as actors of epigenetics and synaptic plasticity to give chance to produce more efficacious treatments and retain its competitiveness against the new high-tech medications like neuroprosthetics, gene, and cell therapy. To increase the success rate in the clinic, the potential targets raised by basic research should be validated in preclinical animal models before launching industrial drug development projects.
大脑紊乱是本世纪最大的健康挑战,迫切需要新的、高效的药物。本文讨论了神经精神药物发现如何应对这一日益增长的需求。
目前的精神药理学武器库依赖于几十年前发现的靶点。此外,目前潜在认知增强剂的主要部分也包含具有多种未被临床适当验证的失败作用模式的化合物。此外,还应考虑预防性药理学的可行性限制。神经影像学和遗传研究的进展强调了表观遗传调控和突触可塑性作为神经精神疾病药物干预的潜在“热点”。然而,与此同时,新的、快速发展的技术已经产生了替代治疗选择,如脑刺激、细胞和基因治疗。
神经精神药物发现应该转向非神经递质相关的靶点,如表观遗传学和突触可塑性的作用因子,以有机会产生更有效的治疗方法,并保持其对神经假肢、基因和细胞治疗等新高科技药物的竞争力。为了提高临床成功率,在启动工业药物开发项目之前,应该在临床前动物模型中验证基础研究提出的潜在靶点。