Abstract

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.

Highlights

  • Central nervous system (CNS) disorders are currently estimated to affect hundreds of millions of people worldwide [1]

  • It is often thought that the blood–brain barrier (BBB) hampers the adequate distribution of CNS drugs into the brain resulting in a lack of effects [2,3,4]

  • This cannot be the sole reason because other factors besides BBB transport determine the concentration-time profile of the unbound drug at the brain target site [5]

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Summary

Introduction

Central nervous system (CNS) disorders are currently estimated to affect hundreds of millions of people worldwide [1]. Other important factors are plasma pharmacokinetics, plasma protein binding, cerebral blood flow, effective brain capillary surface area, blood-cerebrospinal fluid-barrier (BCSFB) transport, intracerebral distribution, CSF turnover, extracellular fluid (ECF) bulk flow, extra-intracellular exchange, brain tissue binding, and drug metabolism [5]. These factors are controlled by many processes, each of which has a specific influence [6], thereby playing a more or less important role in delivering the CNS drug to the right place, at the right time, and at the right concentration. An integrative physiological approach is needed to understand concentration-effect relationships [91]

Conclusion
Conclusions
World Health Organization: “Neurological Disorders
25. Segal MB
28. Oldendorf WH
42. Cserr HF
64. Begley DJ
Findings
70. Girardin F
Full Text
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