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INTRODUCTION

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The brain is a complex assembly of interacting cells that regulate many of life’s activities in a dynamic fashion, generally through the communication process of chemical neurotransmission. Because the CNS drives so many physiological responses, it stands to reason that centrally-acting drugs are invaluable for a plethora of conditions. CNS-acting drugs are used not only to treat anxiety, depression, mania, and schizophrenia, but also to target diverse pathophysiological conditions, such as pain, fever, movement disorders, insomnia, eating disorders, nausea, vomiting, and migraine. However, as the CNS dictates such diverse physiology, the recreational use of some CNS-acting drugs can lead to physical dependence (Chapter 24) with enormous societal impacts. The sheer breadth of physiological and pathological activities mediated by drug molecules acting in the CNS makes this class of therapeutics both wide-ranging and immeasurably important.

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The identification of CNS targets, as well as the development of drug molecules for those targets, presents extraordinary scientific challenges. While years of investigation have begun to dissect the cellular and molecular bases for many aspects of neuronal signaling, complete understanding of the functions of the human brain remains in its infancy. Complicating the effort is the fact that a CNS-active drug may act at multiple sites with disparate and even opposing effects. Furthermore, many CNS disorders likely involve multiple brain regions and pathways, which can frustrate efforts focusing on a single therapeutic agent.

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The pharmacology of CNS-acting drugs is primarily driven by two broad and overlapping goals:

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  • to develop/use drugs as probe compounds to both elucidate and ­manipulate the normal CNS; and

  • to develop drugs to correct pathophysiological changes in the abnormal CNS.

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Modern advances in molecular biology, neurophysiology, structural biology, epigenetics, biomarkers, immunity, and an array of other fields have facilitated both our understanding of the brain and the development of an ever-expanding repertoire of drugs that can selectively treat diseases of the CNS.

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This chapter introduces fundamental principles and guidelines for the comprehensive study of drugs that affect the CNS. Specific therapeutic approaches to neurological and psychiatric disorders are discussed in subsequent chapters. For further detail, see specialized texts (Brady et al., 2012; Kandel et al., 2013; Nestler et al., 2015; Sibley, 2007). Detailed information on nearly all specific receptors and ion channels can be found at the official databases of the IUPHAR/BPS Guide to Pharmacology (http://www.guidetopharmacology.org).

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ABBREVIATIONS

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Abbreviations

AC: adenylyl cyclase

ACh: acetylcholine

ACTH: corticotropin (formerly adrenocorticotropic hormone)

ADHD: attention-deficit/hyperactivity disorder

AMPA: α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid

AP: action potential

BBB: blood-brain barrier

BDNF: brain-derived neurotrophic factor

cAMP: cyclic adenosine monophosphate

CFTR channel: cystic fibrosis transmembrane conductance regulated channel

CGRP: calcitonin gene–related peptide

CLC: chloride channel

CLIP: corticotropin-like intermediate lobe peptide

CNG channel: cyclic nucleotide–gated channel

CNS: central nervous system

CO: carbon monoxide

COX: cyclooxygenase

CSF: cerebrospinal fluid

CYP: cytochrome P450

DA: dopamine

DAG: diacylglycerol

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