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GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors

GPR88 is an orphan G-protein-coupled receptor highly expressed in striatal dopamine D(1) (receptor) R- and D2R-expressing medium spiny neurons. This receptor is involved in activity and motor responses, and we previously showed that this receptor also regulates anxiety-like behaviors. To determine w...

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Autores principales: Meirsman, Aura Carole, Robé, Anne, de Kerchove d’Exaerde, Alban, Kieffer, Brigitte Lina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987659/
https://www.ncbi.nlm.nih.gov/pubmed/27570825
http://dx.doi.org/10.1523/ENEURO.0202-16.2016
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author Meirsman, Aura Carole
Robé, Anne
de Kerchove d’Exaerde, Alban
Kieffer, Brigitte Lina
author_facet Meirsman, Aura Carole
Robé, Anne
de Kerchove d’Exaerde, Alban
Kieffer, Brigitte Lina
author_sort Meirsman, Aura Carole
collection PubMed
description GPR88 is an orphan G-protein-coupled receptor highly expressed in striatal dopamine D(1) (receptor) R- and D2R-expressing medium spiny neurons. This receptor is involved in activity and motor responses, and we previously showed that this receptor also regulates anxiety-like behaviors. To determine whether GPR88 in D2R-expressing neurons contributes to this emotional phenotype, we generated conditional Gpr88 knock-out mice using adenosine A(2A)R (A(2A)R)-Cre-driven recombination, and compared anxiety-related responses in both total and A(2A)R-Gpr88 KO mice. A(2A)R-Gpr88 KO mice showed a selective reduction of Gpr88 mRNA in D2R-expressing, but not D(1)R-expressing, neurons. These mutant mice showed increased locomotor activity and decreased anxiety-like behaviors in light/dark and elevated plus maze tests. These phenotypes were superimposable on those observed in total Gpr88 KO mice, demonstrating that the previously reported anxiogenic activity of GPR88 operates at the level of A(2A)R-expressing neurons. Further, A(2A)R-Gpr88 KO mice showed no change in novelty preference and novelty-suppressed feeding, while these responses were increased and decreased, respectively, in the total Gpr88 KO mice. Also, A(2A)R-Gpr88 KO mice showed intact fear conditioning, while the fear responses were decreased in total Gpr88 KO. We therefore also show for the first time that GPR88 activity regulates approach behaviors and conditional fear; however, these behaviors do not seem mediated by receptors in A(2A)R neurons. We conclude that Gpr88 expressed in A(2A)R neurons enhances ethological anxiety-like behaviors without affecting conflict anxiety and fear responses.
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spelling pubmed-49876592016-08-26 GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors Meirsman, Aura Carole Robé, Anne de Kerchove d’Exaerde, Alban Kieffer, Brigitte Lina eNeuro New Research GPR88 is an orphan G-protein-coupled receptor highly expressed in striatal dopamine D(1) (receptor) R- and D2R-expressing medium spiny neurons. This receptor is involved in activity and motor responses, and we previously showed that this receptor also regulates anxiety-like behaviors. To determine whether GPR88 in D2R-expressing neurons contributes to this emotional phenotype, we generated conditional Gpr88 knock-out mice using adenosine A(2A)R (A(2A)R)-Cre-driven recombination, and compared anxiety-related responses in both total and A(2A)R-Gpr88 KO mice. A(2A)R-Gpr88 KO mice showed a selective reduction of Gpr88 mRNA in D2R-expressing, but not D(1)R-expressing, neurons. These mutant mice showed increased locomotor activity and decreased anxiety-like behaviors in light/dark and elevated plus maze tests. These phenotypes were superimposable on those observed in total Gpr88 KO mice, demonstrating that the previously reported anxiogenic activity of GPR88 operates at the level of A(2A)R-expressing neurons. Further, A(2A)R-Gpr88 KO mice showed no change in novelty preference and novelty-suppressed feeding, while these responses were increased and decreased, respectively, in the total Gpr88 KO mice. Also, A(2A)R-Gpr88 KO mice showed intact fear conditioning, while the fear responses were decreased in total Gpr88 KO. We therefore also show for the first time that GPR88 activity regulates approach behaviors and conditional fear; however, these behaviors do not seem mediated by receptors in A(2A)R neurons. We conclude that Gpr88 expressed in A(2A)R neurons enhances ethological anxiety-like behaviors without affecting conflict anxiety and fear responses. Society for Neuroscience 2016-08-17 /pmc/articles/PMC4987659/ /pubmed/27570825 http://dx.doi.org/10.1523/ENEURO.0202-16.2016 Text en Copyright © 2016 Meirsman et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Meirsman, Aura Carole
Robé, Anne
de Kerchove d’Exaerde, Alban
Kieffer, Brigitte Lina
GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors
title GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors
title_full GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors
title_fullStr GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors
title_full_unstemmed GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors
title_short GPR88 in A(2A)R Neurons Enhances Anxiety-Like Behaviors
title_sort gpr88 in a(2a)r neurons enhances anxiety-like behaviors
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987659/
https://www.ncbi.nlm.nih.gov/pubmed/27570825
http://dx.doi.org/10.1523/ENEURO.0202-16.2016
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