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The mastermind approach to CNS drug therapy: translational prediction of human brain distribution target site kinetics and therapeutic effects

机译:CNS药物治疗的策划方法:人脑分布目标部位动力学和治疗效果的翻译预测

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摘要

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.
机译:尽管CNS研究取得了巨大进步,但CNS疾病仍然是世界上导致残疾的主要原因。与几乎所有其他疾病的总和相比,这意味着更多的住院治疗和更长时间的护理,并表明对良好的CNS药物和药物疗法的高度未满足需求。在给药后,不仅是药物的化学性质和血脑屏障(BBB)转运,但是许多其他过程最终将决定大脑目标部位的动力学,进而决定中枢神经系统的作用。所有这些过程的速率和程度都是动态调节的,因此取决于条件。因此,CNS药物治疗中经常会遇到物种,性别,遗传背景,组织,年龄,饮食,疾病,药物治疗等异质性条件,导致个体间和个体内的巨大差异。应该“在正确的位置,正确的时间,正确的位置”访问CNS。为了改善中枢神经系统疗法和药物开发,需要物种间和条件间差异的细节,以使目标部位的药代动力学和相关的中枢神经系统作用能够在物种之间和疾病状态之间转换。具体而言,此类研究需要包括有关驱动作用的未结合药物浓度的信息。迄今为止,可以在大脑中获得未结合药物浓度的唯一技术是微透析。这种(最少)侵入性技术无法轻易地应用于人类,我们需要依靠翻译方法来预测人脑分布,目标部位动力学和中枢神经系统药物的治疗效果。在本文中,引入了“策划方法”一词,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的CNS药物研究。以这种方式,可以获得关于个体过程中动物给药和中枢神经系统作用之间因果关系的贡献和变异性的知识,这些因果关系可以转化为人类状况。在一些基于临床前微透析的高级研究的基础上,将显示“ Mastermind方法”具有预测人类CNS药物作用的巨大潜力。

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