Medical Journals

Rat Nucleus Accumbens Neurons Persistently Encode Locations Associated with Morphine Reward.

Authors:
  • German Paul W
  • Fields Howard L

From: Neuroscience Graduate Program, Department of Neurologyiology, University of California, San Francisco, California, USA. german@phy.ucsf.edu

Journal of neurophysiology

  • Publish Date: Mar 2007
  • ISSN: 0022-3077
  • Volume: 97
  • Issue: 3
  • Pages: 2094-106
  • Medium: Print
  • Language: English
  • Citation (JAMA): German Paul W, Fields Howard L, et al. Rat Nucleus Accumbens Neurons Persistently Encode Locations Associated with Morphine Reward.. J. Neurophysiol. Mar 2007;97:2094-106

Abstract

When rats and mice are free to explore a familiar environment they spend more time in a previously rewarded location. This conditioned place preference (CPP) results from an increased probability of initiating transitions from an unrewarded location to one previously paired with reward. We recorded nucleus accumbens (NAc) neurons while rats explored a three-room in-line apparatus. Before place conditioning, approximately equal proportions of NAc neurons show excitations or inhibitions when the rat is in each of the rooms (morphine paired, center or saline paired). Conditioning increased the proportion of neurons inhibited while the rat was in the morphine room and neurons excited in the saline room. Many of the neurons in these two groups responded during room transitions. Furthermore, the postconditioning increase in the population of neurons with room-selective responding persisted for several weeks after the last morphine treatment. This long-lasting change in population responses of NAc neurons to initially neutral locations is a neural correlate of the change in location preference manifest as CPP.

Mesh Headings (Keywords): Action Potentials, Analysis of Variance, Animals, Behavior, Animal, Conditioning, Operant, Male, Morphine, Narcotics, Neurons, Nucleus Accumbens, Rats, Rats, Long-Evans, Reward


Check for Full Text / PubMed Unique Identifier (PMID): 17093128


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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