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Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs

Studies in humans suggest that stronger incentive motivational responses to Pavlovian food cues may drive over-consumption leading to and maintaining obesity, particularly in susceptible individuals. However, whether this enhanced incentive motivation emerges as a consequence of obesity or rather pr...

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Autores principales: Derman, Rifka C., Ferrario, Carrie R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010194/
https://www.ncbi.nlm.nih.gov/pubmed/29291424
http://dx.doi.org/10.1016/j.neuropharm.2017.12.039
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author Derman, Rifka C.
Ferrario, Carrie R.
author_facet Derman, Rifka C.
Ferrario, Carrie R.
author_sort Derman, Rifka C.
collection PubMed
description Studies in humans suggest that stronger incentive motivational responses to Pavlovian food cues may drive over-consumption leading to and maintaining obesity, particularly in susceptible individuals. However, whether this enhanced incentive motivation emerges as a consequence of obesity or rather precedes obesity is unknown. Moreover, while human imaging studies have provided important information about differences in striatal responsiveness between susceptible and non-susceptible individuals, the neural mechanisms mediating these behavioral differences are unknown. The Nucleus Accumbens (NAc) mediates cue-triggered reward seeking and activity in the NAc is enhanced in obesity-susceptible populations. Therefore here, we used selectively-bred obesity-prone and obesity-resistant rats to examine intrinsic differences in incentive motivation, and the role of NAc AMPARs in the expression of these behaviors prior to obesity. We found that obesity-prone rats exhibit robust cue-triggered food-seeking (Pavlovian-to-instrumental transfer, PIT). Using intra-NAc infusion of AMPAR antagonists, we show that this behavior is selectively mediated by CP-AMPARs in the NAc core. Additionally, biochemical data suggest that this is due in part to experience-induced increases in CP-AMPAR surface expression in the NAc of obesity-prone rats. In contrast, in obesity-resistant rats PIT was weak and unreliable and training did not increase NAc AMPAR surface expression. Collectively, these data show that food cues acquire greater incentive motivational control in obesity-susceptible populations prior to the development of obesity. This provides support to the idea that enhanced intrinsic incentive motivation may be a contributing factor, rather than a consequence of obesity. In addition, these data demonstrate a novel role for experience-induced up-regulation of NAc CP-AMPARs in PIT, pointing to potential mechanistic parallels between the processes leading to addiction and to obesity.
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spelling pubmed-60101942018-06-20 Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs Derman, Rifka C. Ferrario, Carrie R. Neuropharmacology Article Studies in humans suggest that stronger incentive motivational responses to Pavlovian food cues may drive over-consumption leading to and maintaining obesity, particularly in susceptible individuals. However, whether this enhanced incentive motivation emerges as a consequence of obesity or rather precedes obesity is unknown. Moreover, while human imaging studies have provided important information about differences in striatal responsiveness between susceptible and non-susceptible individuals, the neural mechanisms mediating these behavioral differences are unknown. The Nucleus Accumbens (NAc) mediates cue-triggered reward seeking and activity in the NAc is enhanced in obesity-susceptible populations. Therefore here, we used selectively-bred obesity-prone and obesity-resistant rats to examine intrinsic differences in incentive motivation, and the role of NAc AMPARs in the expression of these behaviors prior to obesity. We found that obesity-prone rats exhibit robust cue-triggered food-seeking (Pavlovian-to-instrumental transfer, PIT). Using intra-NAc infusion of AMPAR antagonists, we show that this behavior is selectively mediated by CP-AMPARs in the NAc core. Additionally, biochemical data suggest that this is due in part to experience-induced increases in CP-AMPAR surface expression in the NAc of obesity-prone rats. In contrast, in obesity-resistant rats PIT was weak and unreliable and training did not increase NAc AMPAR surface expression. Collectively, these data show that food cues acquire greater incentive motivational control in obesity-susceptible populations prior to the development of obesity. This provides support to the idea that enhanced intrinsic incentive motivation may be a contributing factor, rather than a consequence of obesity. In addition, these data demonstrate a novel role for experience-induced up-regulation of NAc CP-AMPARs in PIT, pointing to potential mechanistic parallels between the processes leading to addiction and to obesity. 2017-12-29 2018-03-15 /pmc/articles/PMC6010194/ /pubmed/29291424 http://dx.doi.org/10.1016/j.neuropharm.2017.12.039 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Derman, Rifka C.
Ferrario, Carrie R.
Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs
title Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs
title_full Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs
title_fullStr Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs
title_full_unstemmed Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs
title_short Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs
title_sort enhanced incentive motivation in obesity-prone rats is mediated by nac core cp-ampars
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010194/
https://www.ncbi.nlm.nih.gov/pubmed/29291424
http://dx.doi.org/10.1016/j.neuropharm.2017.12.039
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