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The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice

The GluA1 subunit of the AMPA receptor has been implicated in anhedonia. Mice that lack GluA1 (Gria1 knockout mice) show reduced lick cluster size, a measure of palatability in feeding behaviour. This deficit may reflect a role for GluA1 in encoding the hedonic value of palatable substances or inste...

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Autores principales: Strickland, Jasmin A., Austen, Joseph M., Sprengel, Rolf, Sanderson, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768090/
https://www.ncbi.nlm.nih.gov/pubmed/33058902
http://dx.doi.org/10.1016/j.physbeh.2020.113206
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author Strickland, Jasmin A.
Austen, Joseph M.
Sprengel, Rolf
Sanderson, David J.
author_facet Strickland, Jasmin A.
Austen, Joseph M.
Sprengel, Rolf
Sanderson, David J.
author_sort Strickland, Jasmin A.
collection PubMed
description The GluA1 subunit of the AMPA receptor has been implicated in anhedonia. Mice that lack GluA1 (Gria1 knockout mice) show reduced lick cluster size, a measure of palatability in feeding behaviour. This deficit may reflect a role for GluA1 in encoding the hedonic value of palatable substances or instead a role for GluA1 in the behavioural expression of hedonic value. We tested the role of GluA1 in hedonic value by assessing sensitivity to changes in the rewarding property of sucrose as a consequence of negative/positive contrast effects in female mice. During training, on half of the days consumption of a flavour (CS+) mixed with 4% sucrose was preceded by consumption of 1% sucrose (positive contrast). On the other half of days consumption of a different flavour (CS–) mixed with 4% sucrose was preceded by consumption of 16% sucrose (negative contrast). In the test session both wild-type, controls and Gria1 knockout mice consumed more of the CS+ flavour than the CS– flavour. While Gria1 knockout mice showed reduced lick cluster sizes, both genotypes made larger lick clusters for the CS+ flavour than the CS– flavour suggesting that the CS+ was more palatable than the CS–. A follow up experiment in normal mice demonstrated that the negative contrast procedure resulted in a conditioned reduction of palatability of the CS– in comparison to an associatively neutral, novel flavour. The results failed to demonstrate a role for GluA1 in hedonic value suggesting that, instead, GluA1 is necessary for hedonic responding.
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spelling pubmed-77680902021-01-01 The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice Strickland, Jasmin A. Austen, Joseph M. Sprengel, Rolf Sanderson, David J. Physiol Behav Article The GluA1 subunit of the AMPA receptor has been implicated in anhedonia. Mice that lack GluA1 (Gria1 knockout mice) show reduced lick cluster size, a measure of palatability in feeding behaviour. This deficit may reflect a role for GluA1 in encoding the hedonic value of palatable substances or instead a role for GluA1 in the behavioural expression of hedonic value. We tested the role of GluA1 in hedonic value by assessing sensitivity to changes in the rewarding property of sucrose as a consequence of negative/positive contrast effects in female mice. During training, on half of the days consumption of a flavour (CS+) mixed with 4% sucrose was preceded by consumption of 1% sucrose (positive contrast). On the other half of days consumption of a different flavour (CS–) mixed with 4% sucrose was preceded by consumption of 16% sucrose (negative contrast). In the test session both wild-type, controls and Gria1 knockout mice consumed more of the CS+ flavour than the CS– flavour. While Gria1 knockout mice showed reduced lick cluster sizes, both genotypes made larger lick clusters for the CS+ flavour than the CS– flavour suggesting that the CS+ was more palatable than the CS–. A follow up experiment in normal mice demonstrated that the negative contrast procedure resulted in a conditioned reduction of palatability of the CS– in comparison to an associatively neutral, novel flavour. The results failed to demonstrate a role for GluA1 in hedonic value suggesting that, instead, GluA1 is necessary for hedonic responding. Elsevier Science 2021-01-01 /pmc/articles/PMC7768090/ /pubmed/33058902 http://dx.doi.org/10.1016/j.physbeh.2020.113206 Text en © 2020 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Strickland, Jasmin A.
Austen, Joseph M.
Sprengel, Rolf
Sanderson, David J.
The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice
title The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice
title_full The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice
title_fullStr The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice
title_full_unstemmed The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice
title_short The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice
title_sort glua1 ampar subunit is necessary for hedonic responding but not hedonic value in female mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768090/
https://www.ncbi.nlm.nih.gov/pubmed/33058902
http://dx.doi.org/10.1016/j.physbeh.2020.113206
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