4.5 Article

D-SERINE TREATMENT REDUCES COCAINE-PRIMED REINSTATEMENT IN RATS FOLLOWING EXTENDED ACCESS TO COCAINE SELF-ADMINISTRATION

Journal

NEUROSCIENCE
Volume 169, Issue 3, Pages 1127-1135

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2010.06.006

Keywords

cocaine; self-administration; reinstatement; D-serine; NMDA receptor

Categories

Funding

  1. National Institutes of Health National Institute on Drug Abuse [DA016302]
  2. University of Georgia

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The most intractable feature of drug addiction is the high rate of relapse, even following extended periods of abstinence from drug-taking. Evidence suggests that allowing rats extended access to cocaine self-administration leads to behavioral characteristics in these animals that are consistent with the development of addiction in humans. In the current study, rats were allowed to self-administer cocaine over a total of 22 daily sessions, the final seven of which were long-access (LgA) sessions of 6 h duration. Assessments of reinstatement of drug-seeking behavior were made following reintroduction to the drug-taking environment and noncontingent priming with either conditioned stimulus (CS) or cocaine in both extinguished and abstinent subject groups. Three separate groups of rats were treated with either saline or D-serine (100 mg/kg i.p.) administered 2 h prior to, or immediately following, each extinction training session. Saline-treated LgA rats were resistant to the effects of extinction training to reduce noncontingent priming of reinstatement of drug-seeking behavior with either CS or cocaine. In contrast, treatment with D-serine either before or immediately following the sessions resulted in a significant enhancement in the ability of extinction training to reduce cocaine-primed reinstatement of drug-seeking behavior. These results suggest that D-serine can act to enhance the consolidation of extinction learning in LgA rats, and is therefore a promising adjunctive agent along with behavioral therapy for the treatment of cocaine addiction. (C) 2010 IBRO. Published by Elsevier Ltd. All rights reserved.

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