AI Article Synopsis

  • The study examines the role of glucocorticoid receptors (GRs) in morphine-induced conditioned place preference (CPP) and how they influence reward memory in different brain regions.
  • Researchers used a GR antagonist, RU38486, to assess its impact on various phases of reward memory, specifically acquisition, retrieval, and reconsolidation of CPP behavior.
  • Findings indicate that RU38486 disrupts these phases of reward memory without independently causing CPP or conditioned place aversion, shedding light on how glucocorticoids affect drug-related reward behaviors.

Article Abstract

Association between the reward caused by consuming drugs and the context in which they are consumed is essential in the formation of morphine-induced conditioned place preference (CPP). Glucocorticoid receptor (GRs) activation in different regions of the brain affects reward-based reinforcement and memory processing. A wide array of studies have demonstrated that blockage of GRs in some brain areas can have an effect on reward-related memory; however, to date there have been no systematic studies about the involvement of glucocorticoids (GCs) in morphine-related reward memory. Here, we used the GR antagonist RU38486 to investigate how GRs blockage affects the sensitization and CPP behavior during different phases of reward memory included acquisition, retrieval and reconsolidation. Interestingly, our results showed RU38486 has the ability to impair the acquisition, retrieval and reconsolidation of reward-based memory in CPP and sensitization behavior. But RU38486 by itself cannot induce CPP or conditioned place aversion (CPA) behavior. Our data provide a much more complete picture of the potential effects that glucocorticoids have on the reward memory of different phases and inhibit the sensitization behavior.

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Source
http://dx.doi.org/10.3724/SP.J.1141.2013.E01E26DOI Listing

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