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Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors
Metabotropic glutamate 5 receptors (mGlu(5)) are thought to play an important role in mediating emotional information processing. In particular, negative allosteric modulators (NAMs) of mGlu(5) have received a lot of attention as potential novel treatments for several neuropsychiatric diseases, incl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688906/ https://www.ncbi.nlm.nih.gov/pubmed/36428984 http://dx.doi.org/10.3390/cells11223555 |
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author | Matulewicz, Pawel Ramos-Prats, Arnau Gómez-Santacana, Xavier Llebaria, Amadeu Ferraguti, Francesco |
author_facet | Matulewicz, Pawel Ramos-Prats, Arnau Gómez-Santacana, Xavier Llebaria, Amadeu Ferraguti, Francesco |
author_sort | Matulewicz, Pawel |
collection | PubMed |
description | Metabotropic glutamate 5 receptors (mGlu(5)) are thought to play an important role in mediating emotional information processing. In particular, negative allosteric modulators (NAMs) of mGlu(5) have received a lot of attention as potential novel treatments for several neuropsychiatric diseases, including anxiety-related disorders. The aim of this study was to assess the influence of pre- and post-training mGlu(5) inactivation in cued fear conditioned mice on neuronal oscillatory activity during fear retrieval. For this study we used the recently developed mGlu(5) NAM Alloswicth-1 administered systemically. Injection of Alloswicth-1 before, but not after, fear conditioning resulted in a significant decrease in freezing upon fear retrieval. Mice injected with Alloswicth-1 pre-training were also implanted with recording microelectrodes into both the medial prefrontal cortex (mPFC) and ventral hippocampus (vHPC). The recordings revealed a reduction in theta rhythmic activity (4–12 Hz) in both the mPFC and vHPC during fear retrieval. These results indicate that inhibition of mGlu(5) signaling alters local oscillatory activity in principal components of the fear brain network underlying a reduced response to a predicted threat. |
format | Online Article Text |
id | pubmed-9688906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96889062022-11-25 Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors Matulewicz, Pawel Ramos-Prats, Arnau Gómez-Santacana, Xavier Llebaria, Amadeu Ferraguti, Francesco Cells Article Metabotropic glutamate 5 receptors (mGlu(5)) are thought to play an important role in mediating emotional information processing. In particular, negative allosteric modulators (NAMs) of mGlu(5) have received a lot of attention as potential novel treatments for several neuropsychiatric diseases, including anxiety-related disorders. The aim of this study was to assess the influence of pre- and post-training mGlu(5) inactivation in cued fear conditioned mice on neuronal oscillatory activity during fear retrieval. For this study we used the recently developed mGlu(5) NAM Alloswicth-1 administered systemically. Injection of Alloswicth-1 before, but not after, fear conditioning resulted in a significant decrease in freezing upon fear retrieval. Mice injected with Alloswicth-1 pre-training were also implanted with recording microelectrodes into both the medial prefrontal cortex (mPFC) and ventral hippocampus (vHPC). The recordings revealed a reduction in theta rhythmic activity (4–12 Hz) in both the mPFC and vHPC during fear retrieval. These results indicate that inhibition of mGlu(5) signaling alters local oscillatory activity in principal components of the fear brain network underlying a reduced response to a predicted threat. MDPI 2022-11-10 /pmc/articles/PMC9688906/ /pubmed/36428984 http://dx.doi.org/10.3390/cells11223555 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Matulewicz, Pawel Ramos-Prats, Arnau Gómez-Santacana, Xavier Llebaria, Amadeu Ferraguti, Francesco Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors |
title | Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors |
title_full | Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors |
title_fullStr | Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors |
title_full_unstemmed | Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors |
title_short | Control of Theta Oscillatory Activity Underlying Fear Expression by mGlu(5) Receptors |
title_sort | control of theta oscillatory activity underlying fear expression by mglu(5) receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688906/ https://www.ncbi.nlm.nih.gov/pubmed/36428984 http://dx.doi.org/10.3390/cells11223555 |
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