Publication

The behavioral pharmacology of hallucinogens

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Last modified
  • 02/20/2025
Type of Material
Authors
    William E. Fantegrossi, Emory UniversityAeneas C. Murnane, Emory UniversityChad J. Reissig, Johns Hopkins University
Language
  • English
Date
  • 2008-01-01
Publisher
  • Elsevier: 12 months
Publication Version
Copyright Statement
  • © 2007 Elsevier Inc. All rights reserved.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0006-2952
Volume
  • 75
Issue
  • 1
Start Page
  • 17
End Page
  • 33
Grant/Funding Information
  • The authors acknowledge the generous funding provided by USPHS Grant DA020645 and by the College on Problems of Drug Dependence.
Abstract
  • Until very recently, comparatively few scientists were studying hallucinogenic drugs. Nevertheless, selective antagonists are available for relevant serotonergic receptors, the majority of which have now been cloned, allowing for reasonably thorough pharmacological investigation. Animal models sensitive to the behavioral effects of the hallucinogens have been established and exploited. Sophisticated genetic techniques have enabled the development of mutant mice, which have proven useful in the study of hallucinogens. The capacity to study post-receptor signaling events has lead to the proposal of a plausible mechanism of action for these compounds. The tools currently available to study the hallucinogens are thus more plentiful and scientifically advanced than were those accessible to earlier researchers studying the opioids, benzodiazepines, cholinergics, or other centrally active compounds. The behavioral pharmacology of phenethylamine, tryptamine, and ergoline hallucinogens are described in this review, paying particular attention to important structure activity relationships which have emerged, receptors involved in their various actions, effects on conditioned and unconditioned behaviors, and in some cases, human psychopharmacology. As clinical interest in the therapeutic potential of these compounds is once again beginning to emerge, it is important to recognize the wealth of data derived from controlled preclinical studies on these compounds.
Author Notes
  • Correspondence: William E. Fantegrossi, Division of Neuroscience Yerkes National Primate Research Center 954 Gatewood Road NE Atlanta, GA 30322, USA; Email: wfanteg@emory.edu; Tel: (404) 727−8512; Fax: (404) 727−1266
Keywords
Research Categories
  • Chemistry, Biochemistry
  • Psychology, Behavioral
  • Health Sciences, Pharmacology

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