Division of Pharmacology, Leiden-Academic Center for Drug Research, Leiden University, Leiden, the Netherlands.
Fluids Barriers CNS. 2013 Feb 22;10(1):12. doi: 10.1186/2045-8118-10-12.
Despite enormous advances in CNS research, CNS disorders remain the world's leading cause of disability. This accounts for more hospitalizations and prolonged care than almost all other diseases combined, and indicates a high unmet need for good CNS drugs and drug therapies.Following dosing, not only the chemical properties of the drug and blood-brain barrier (BBB) transport, but also many other processes will ultimately determine brain target site kinetics and consequently the CNS effects. The rate and extent of all these processes are regulated dynamically, and thus condition dependent. Therefore, heterogenious conditions such as species, gender, genetic background, tissue, age, diet, disease, drug treatment etc., result in considerable inter-individual and intra-individual variation, often encountered in CNS drug therapy.For effective therapy, drugs should access the CNS "at the right place, at the right time, and at the right concentration". To improve CNS therapies and drug development, details of inter-species and inter-condition variations are needed to enable target site pharmacokinetics and associated CNS effects to be translated between species and between disease states. Specifically, such studies need to include information about unbound drug concentrations which drive the effects. To date the only technique that can obtain unbound drug concentrations in brain is microdialysis. This (minimally) invasive technique cannot be readily applied to humans, and we need to rely on translational approaches to predict human brain distribution, target site kinetics, and therapeutic effects of CNS drugs.In this review the term "Mastermind approach" is introduced, for strategic and systematic CNS drug research using advanced preclinical experimental designs and mathematical modeling. In this way, knowledge can be obtained about the contributions and variability of individual processes on the causal path between drug dosing and CNS effect in animals that can be translated to the human situation. On the basis of a few advanced preclinical microdialysis based investigations it will be shown that the "Mastermind approach" has a high potential for the prediction of human CNS drug effects.
尽管中枢神经系统(CNS)研究取得了巨大进展,但 CNS 疾病仍然是全球致残的主要原因。这导致的住院和长期护理比几乎所有其他疾病的总和还要多,表明对良好的 CNS 药物和药物治疗存在巨大的未满足需求。给药后,不仅药物的化学性质和血脑屏障(BBB)转运,还有许多其他过程最终将决定脑靶部位动力学,并因此影响 CNS 效应。所有这些过程的速度和程度都是动态调节的,因此取决于条件。因此,物种、性别、遗传背景、组织、年龄、饮食、疾病、药物治疗等异质条件会导致相当大的个体间和个体内差异,这在 CNS 药物治疗中经常遇到。为了进行有效的治疗,药物应该“在正确的位置、正确的时间、正确的浓度”进入 CNS。为了改善 CNS 治疗和药物开发,需要详细了解种间和条件间的变化,以便在物种间和疾病状态间对靶部位药代动力学和相关的 CNS 效应进行转化。具体而言,此类研究需要包括驱动效应的未结合药物浓度的信息。迄今为止,唯一能够获得大脑中未结合药物浓度的技术是微透析。这种(最小程度的)侵入性技术不能轻易应用于人类,我们需要依赖转化方法来预测 CNS 药物在人类大脑中的分布、靶部位动力学和治疗效果。在本文中,引入了“掌控全局方法”这一术语,用于使用先进的临床前实验设计和数学模型进行战略性和系统性的 CNS 药物研究。通过这种方式,可以获得关于动物中药物剂量与 CNS 效应之间因果关系中各个过程的贡献和变异性的知识,然后可以将这些知识转化为人类情况。基于少数先进的基于微透析的临床前研究,将表明“掌控全局方法”在预测人类 CNS 药物效应方面具有很高的潜力。