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Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model

Peripheral mechanoreceptor-based treatments such as acupuncture and chiropractic manipulation have shown success in modulating the mesolimbic dopamine (DA) system originating in the ventral tegmental area (VTA) of the midbrain and projecting to the nucleus accumbens (NAc) of the striatum. We have pr...

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Autores principales: Jones, Gavin C., Small, Christina A., Otteson, Dallin Z., Hafen, Caylor W., Breinholt, Jacob T., Flora, Paul D., Burris, Matthew D., Sant, David W., Ruchti, Tysum R., Yorgason, Jordan T., Steffensen, Scott C., Bills, Kyle B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532581/
https://www.ncbi.nlm.nih.gov/pubmed/37762450
http://dx.doi.org/10.3390/ijms241814147
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author Jones, Gavin C.
Small, Christina A.
Otteson, Dallin Z.
Hafen, Caylor W.
Breinholt, Jacob T.
Flora, Paul D.
Burris, Matthew D.
Sant, David W.
Ruchti, Tysum R.
Yorgason, Jordan T.
Steffensen, Scott C.
Bills, Kyle B.
author_facet Jones, Gavin C.
Small, Christina A.
Otteson, Dallin Z.
Hafen, Caylor W.
Breinholt, Jacob T.
Flora, Paul D.
Burris, Matthew D.
Sant, David W.
Ruchti, Tysum R.
Yorgason, Jordan T.
Steffensen, Scott C.
Bills, Kyle B.
author_sort Jones, Gavin C.
collection PubMed
description Peripheral mechanoreceptor-based treatments such as acupuncture and chiropractic manipulation have shown success in modulating the mesolimbic dopamine (DA) system originating in the ventral tegmental area (VTA) of the midbrain and projecting to the nucleus accumbens (NAc) of the striatum. We have previously shown that mechanoreceptor activation via whole-body vibration (WBV) ameliorates neuronal and behavioral effects of chronic ethanol exposure. In this study, we employ a similar paradigm to assess the efficacy of WBV as a preventative measure of neuronal and behavioral effects of morphine withdrawal in a Wistar rat model. We demonstrate that concurrent administration of WBV at 80 Hz with morphine over a 5-day period significantly reduced adaptations in VTA GABA neuronal activity and NAc DA release and modulated expression of δ-opioid receptors (DORs) on NAc cholinergic interneurons (CINs) during withdrawal. We also observed a reduction in behavior typically associated with opioid withdrawal. WBV represents a promising adjunct to current intervention for opioid use disorder (OUD) and should be examined translationally in humans.
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spelling pubmed-105325812023-09-28 Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model Jones, Gavin C. Small, Christina A. Otteson, Dallin Z. Hafen, Caylor W. Breinholt, Jacob T. Flora, Paul D. Burris, Matthew D. Sant, David W. Ruchti, Tysum R. Yorgason, Jordan T. Steffensen, Scott C. Bills, Kyle B. Int J Mol Sci Article Peripheral mechanoreceptor-based treatments such as acupuncture and chiropractic manipulation have shown success in modulating the mesolimbic dopamine (DA) system originating in the ventral tegmental area (VTA) of the midbrain and projecting to the nucleus accumbens (NAc) of the striatum. We have previously shown that mechanoreceptor activation via whole-body vibration (WBV) ameliorates neuronal and behavioral effects of chronic ethanol exposure. In this study, we employ a similar paradigm to assess the efficacy of WBV as a preventative measure of neuronal and behavioral effects of morphine withdrawal in a Wistar rat model. We demonstrate that concurrent administration of WBV at 80 Hz with morphine over a 5-day period significantly reduced adaptations in VTA GABA neuronal activity and NAc DA release and modulated expression of δ-opioid receptors (DORs) on NAc cholinergic interneurons (CINs) during withdrawal. We also observed a reduction in behavior typically associated with opioid withdrawal. WBV represents a promising adjunct to current intervention for opioid use disorder (OUD) and should be examined translationally in humans. MDPI 2023-09-15 /pmc/articles/PMC10532581/ /pubmed/37762450 http://dx.doi.org/10.3390/ijms241814147 Text en © 2023 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
Jones, Gavin C.
Small, Christina A.
Otteson, Dallin Z.
Hafen, Caylor W.
Breinholt, Jacob T.
Flora, Paul D.
Burris, Matthew D.
Sant, David W.
Ruchti, Tysum R.
Yorgason, Jordan T.
Steffensen, Scott C.
Bills, Kyle B.
Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model
title Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model
title_full Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model
title_fullStr Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model
title_full_unstemmed Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model
title_short Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat Model
title_sort whole-body vibration prevents neuronal, neurochemical, and behavioral effects of morphine withdrawal in a rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532581/
https://www.ncbi.nlm.nih.gov/pubmed/37762450
http://dx.doi.org/10.3390/ijms241814147
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