4.2 Article

Serotonin2C receptors and drug addiction: focus on cocaine

Journal

EXPERIMENTAL BRAIN RESEARCH
Volume 230, Issue 4, Pages 537-545

Publisher

SPRINGER
DOI: 10.1007/s00221-013-3593-2

Keywords

5-HT2C receptor; Cocaine; Mesocorticolimbic system; Dopamine; Dependence

Categories

Funding

  1. Institute of Pharmacology (Krakow, Poland)
  2. Department of Toxicology, Faculty of Pharmacy Jagiellonian University (Krakow, Poland)
  3. Institut National de la Recherche et de la Sante (INSERM)
  4. Bordeaux 2 University

Ask authors/readers for more resources

This review provides an overview of the role of central serotonin(2C) (5-HT2C) receptors in drug addiction, specifically focusing on their impact on the neurochemical and behavioral effects of cocaine, one of the most worldwide abused drug. First, we described the neurochemical and electrophysiological mechanisms underlying the interaction between 5-HT2C receptors and the mesocorticolimbic dopaminergic network, in keeping with the key role of this system in drug abuse and dependence. Thereafter, we focused on the role of 5-HT2C receptors in the effects of cocaine in various preclinical behavioral models used in drug addiction research, such as locomotor hyperactivity, locomotor sensitization, drug discrimination, and self-administration, to end with an overview of the neurochemical mechanisms underlying the interactions between 5-HT2C receptors, mesocorticolimbic dopamine system, and cocaine. On their whole, the presented data provide compelling preclinical evidence that 5-HT2C receptor agonists may have efficacy in the treatment of cocaine abuse and dependence, thereby underlying the need for additional clinical studies to ascertain whether preclinical data translate to the human.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available