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PMID: 18639587 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Serotonergic mechanisms in addiction-related memories.

Behavioural brain research ·Vol. 195 ·No. 1 ·2008-12-16 ·Pages 39-53

Nic Dhonnchadha BA, Cunningham KA

Abstract

Drug-associated memories are a hallmark of addiction and a contributing factor in the continued use and relapse to drugs of abuse. Repeated association of drugs of abuse with conditioned stimuli leads to long-lasting behavioral responses that reflect reward-controlled learning and participate in the establishment of addiction. A greater understanding of the mechanisms underlying the formation and retrieval of drug-associated memories may shed light on potential therapeutic approaches to effectively intervene with drug use-associated memory. There is evidence to support the involvement of serotonin (5-HT) neurotransmission in learning and memory formation through the families of the 5-HT(1) receptor (5-HT(1)R) and 5-HT(2)R which have also been shown to play a modulatory role in the behavioral effects induced by many psychostimulants. While there is a paucity of studies examining the effects of selective 5-HT(1A)R ligands, the available dataset suggests that 5-HT(1B)R agonists may inhibit retrieval of cocaine-associated memories. The 5-HT(2A)R and 5-HT(2C)R appear to be integral in the strong conditioned associations made between cocaine and environmental cues with 5-HT(2A)R antagonists and 5-HT(2C)R agonists possessing potency in blocking retrieval of cocaine-associated memories following cocaine self-administration procedures. The complex anatomical connectivity between 5-HT neurons and other neuronal phenotypes in limbic-corticostriatal brain structures, the heterogeneity of 5-HT receptors (5-HT(X)R) and the conflicting results of behavioral experiments which employ non-specific 5-HT(X)R ligands contribute to the complexity of interpreting the involvement of 5-HT systems in addictive-related memory processes. This review briefly traces the history of 5-HT involvement in retrieval of drug-cue associations and future targets of serotonergic manipulation that may reduce the impact that drug cues have on addictive behavior and relapse.

MeSH Terms
Animals Behavior, Addictive/physiopathology Cocaine-Related Disorders/physiopathology Humans Learning/physiology Memory/physiology Receptors, Serotonin/metabolism,physiology Serotonin/metabolism,physiology Synaptic Transmission/physiology
Chemicals
Receptors, Serotonin Serotonin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Nic Dhonnchadha Bríd A
Center for Addiction Research, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Cunningham Kathryn A
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Article Info
Journal
Behavioural brain research
Abbr.
Behav Brain Res
ISSN
1872-7549
Published
2008-12-16
Epub
2008-00-01
Pages
39-53
Language
English
Region
Netherlands
NLM ID
8004872
PMCID
PMC2630382
Subset
IM
Grants
NIDA NIH HHS · K05 DA020087-01 · United States
NIDA NIH HHS · K02 DA000260-05 · United States
NIDA NIH HHS · K05 DA020087-04 · United States
NIDA NIH HHS · R01 DA006511-15 · United States
NIDA NIH HHS · K02 DA000260-09 · United States
NIDA NIH HHS · R01 DA006511-10S1 · United States
NIDA NIH HHS · K02 DA000260-06 · United States
NIDA NIH HHS · R01 DA006511-10 · United States
NIDA NIH HHS · R01 DA006511-13 · United States
NIDA NIH HHS · DA 00260 · United States
NIDA NIH HHS · R01 DA006511-12 · United States
NIDA NIH HHS · DA 06511 · United States
NIDA NIH HHS · K02 DA000260 · United States
NIDA NIH HHS · K05 DA020087-03 · United States
NIDA NIH HHS · K02 DA000260-08 · United States
NIDA NIH HHS · K02 DA000260-04 · United States
NIDA NIH HHS · R01 DA006511 · United States
NIDA NIH HHS · K05 DA 020087 · United States
NIDA NIH HHS · K05 DA020087-02 · United States
NIDA NIH HHS · R01 DA006511-14A1 · United States
NIDA NIH HHS · R01 DA006511-11 · United States
NIDA NIH HHS · R01 DA006511-11S1 · United States
NIDA NIH HHS · K05 DA020087 · United States
NIDA NIH HHS · K02 DA000260-07 · United States
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