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Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test

Traditionally, a reduction in floating behavior or immobility in the Porsolt forced swim test is employed as a predictor of anti-depressant efficacy. However, over the past several years, our studies of alcohol withdrawal-induced negative affect consistently indicate the coincidence of increased anx...

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Autores principales: Lee, Kaziya M, Coelho, Michal A, Sern, Kimberly R, Class, MacKayla A, Bocz, Mark D, Szumlinski, Karen K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584874/
https://www.ncbi.nlm.nih.gov/pubmed/28884167
http://dx.doi.org/10.1177/2470547017712985
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author Lee, Kaziya M
Coelho, Michal A
Sern, Kimberly R
Class, MacKayla A
Bocz, Mark D
Szumlinski, Karen K
author_facet Lee, Kaziya M
Coelho, Michal A
Sern, Kimberly R
Class, MacKayla A
Bocz, Mark D
Szumlinski, Karen K
author_sort Lee, Kaziya M
collection PubMed
description Traditionally, a reduction in floating behavior or immobility in the Porsolt forced swim test is employed as a predictor of anti-depressant efficacy. However, over the past several years, our studies of alcohol withdrawal-induced negative affect consistently indicate the coincidence of increased anxiety-related behaviors on various behavioral tests with reduced immobility in the forced swim test. Further, this behavioral profile correlates with increased mGlu5 protein expression within limbic brain regions. As the role for mGlu5 in anxiety is well established, we hypothesized that the reduced immobility exhibited by alcohol-withdrawn mice when tested in the forced swim test might reflect anxiety, possibly a hyper-reactivity to the acute swim stressor. Herein, we evaluated whether or not the decreased forced swim test immobility during alcohol withdrawal responds to systemic treatment with a behaviorally effective dose of the prototypical anxiolytic, buspirone (5 mg/kg). We also determined the functional relevance of the withdrawal-induced increase in mGlu5 expression for forced swim test behavior by comparing the effects of buspirone to a behaviorally effective dose of the mGlu5 negative allosteric modulator MTEP (3 mg/kg). Adult male C57BL/6J mice were subjected to a 14-day, multi-bottle, binge-drinking protocol that elicits hyper-anxiety and increases glutamate-related protein expression during early withdrawal. Control animals received only water. At 24-h withdrawal, animals from each drinking condition were subdivided into groups and treated with an intraperitoneal injection of buspirone, MTEP, or vehicle, 30 min prior to the forced swim test. Drug effects on general locomotor activity were also assessed. As we reported previously, alcohol-withdrawn animals exhibited significantly reduced immobility in the forced swim test compared to water controls. Both buspirone and MTEP significantly increased immobility in alcohol-withdrawn animals, with a modest increase also seen in water controls. No significant group differences were observed for locomotor activity, indicating that neither anxiolytic was sedating. These results provide predictive validity for increased swimming/reduced immobility in the forced swim test as a model of anxiety and provide novel evidence in favor of mGlu5 inhibition as an effective therapeutic strategy for treating hyper-anxiety during alcohol withdrawal.
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spelling pubmed-55848742017-09-05 Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test Lee, Kaziya M Coelho, Michal A Sern, Kimberly R Class, MacKayla A Bocz, Mark D Szumlinski, Karen K Chronic Stress (Thousand Oaks) Original Article Traditionally, a reduction in floating behavior or immobility in the Porsolt forced swim test is employed as a predictor of anti-depressant efficacy. However, over the past several years, our studies of alcohol withdrawal-induced negative affect consistently indicate the coincidence of increased anxiety-related behaviors on various behavioral tests with reduced immobility in the forced swim test. Further, this behavioral profile correlates with increased mGlu5 protein expression within limbic brain regions. As the role for mGlu5 in anxiety is well established, we hypothesized that the reduced immobility exhibited by alcohol-withdrawn mice when tested in the forced swim test might reflect anxiety, possibly a hyper-reactivity to the acute swim stressor. Herein, we evaluated whether or not the decreased forced swim test immobility during alcohol withdrawal responds to systemic treatment with a behaviorally effective dose of the prototypical anxiolytic, buspirone (5 mg/kg). We also determined the functional relevance of the withdrawal-induced increase in mGlu5 expression for forced swim test behavior by comparing the effects of buspirone to a behaviorally effective dose of the mGlu5 negative allosteric modulator MTEP (3 mg/kg). Adult male C57BL/6J mice were subjected to a 14-day, multi-bottle, binge-drinking protocol that elicits hyper-anxiety and increases glutamate-related protein expression during early withdrawal. Control animals received only water. At 24-h withdrawal, animals from each drinking condition were subdivided into groups and treated with an intraperitoneal injection of buspirone, MTEP, or vehicle, 30 min prior to the forced swim test. Drug effects on general locomotor activity were also assessed. As we reported previously, alcohol-withdrawn animals exhibited significantly reduced immobility in the forced swim test compared to water controls. Both buspirone and MTEP significantly increased immobility in alcohol-withdrawn animals, with a modest increase also seen in water controls. No significant group differences were observed for locomotor activity, indicating that neither anxiolytic was sedating. These results provide predictive validity for increased swimming/reduced immobility in the forced swim test as a model of anxiety and provide novel evidence in favor of mGlu5 inhibition as an effective therapeutic strategy for treating hyper-anxiety during alcohol withdrawal. SAGE Publications 2017-06-27 /pmc/articles/PMC5584874/ /pubmed/28884167 http://dx.doi.org/10.1177/2470547017712985 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Lee, Kaziya M
Coelho, Michal A
Sern, Kimberly R
Class, MacKayla A
Bocz, Mark D
Szumlinski, Karen K
Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test
title Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test
title_full Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test
title_fullStr Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test
title_full_unstemmed Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test
title_short Anxiolytic Effects of Buspirone and MTEP in the Porsolt Forced Swim Test
title_sort anxiolytic effects of buspirone and mtep in the porsolt forced swim test
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584874/
https://www.ncbi.nlm.nih.gov/pubmed/28884167
http://dx.doi.org/10.1177/2470547017712985
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