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      Exploring Reward System Responsivity in the Nucleus Accumbens across Chronicity of Binge Eating in Female Rats

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      , Ph.D. 1 , , Ph.D. 2 , , Ph.D. 2 , , Ph.D. 3
      The International journal of eating disorders

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          Abstract

          Objective

          Research has highlighted the importance of reward-based processes in binge eating (BE). However, both increased and decreased activation have been observed in reward related brain regions for BE. Differences may be similar to addiction research, where the reward system is initially hyper-responsive at early stages of use, but becomes hypo-responsive with prolonged drug/alcohol use. This study was the first to examine differences in reward system responsivity at early versus chronic BE stages.

          Method

          Using an animal model, Sprague-Dawley female rats were identified as BE prone (BEP) or BE resistant (BER) and randomly assigned to an early or chronic stage group. Neural activation (via Fos) was quantified in the nucleus accumbens core (NAC) and shell (NAS).

          Results

          Early stage BEP rats had the highest levels of Fos expression of all of the study groups. By contrast, chronic stage BEP rats exhibited decreased activation in the NAS and NAC that was similar to the activation in chronic stage BER rats.

          Discussion

          Findings are significant in suggesting hyper-neural activation to reward in the early stages of BE and decreased activation in later stages of BE. Additional studies are needed to elucidate how these differences may impact risk for and maintenance of BE.

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          Author and article information

          Journal
          8111226
          2410
          Int J Eat Disord
          Int J Eat Disord
          The International journal of eating disorders
          0276-3478
          1098-108X
          24 May 2018
          29 July 2018
          August 2018
          01 August 2019
          : 51
          : 8
          : 989-993
          Affiliations
          [1 ]Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA
          [2 ]Neuroscience Program, Michigan State University, East Lansing, MI, USA
          [3 ]Department of Psychology, Michigan State University, East Lansing, MI, USA
          Author notes
          Corresponding Author: Kelly L. Klump, Ph.D., Department of Psychology, Michigan State University, 316 Physics Road – room 107B Psychology, East Lansing, MI 48824-1116, PH: 517-432-7281, FAX: 517-432-2476, klump@ 123456msu.edu
          Article
          PMC6230309 PMC6230309 6230309 nihpa969422
          10.1002/eat.22895
          6230309
          30058183
          79143f06-c8e0-45a8-8a60-b9799f5e61a3
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