Cargando…
The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats
RATIONALE: Opioid drugs indirectly activate dopamine (DA) neurons in the ventral tegmental area (VTA) through a disinhibition mechanism mediated by mu opioid receptors (MORs) present both on the GABA projection neurons located in the medial tegmental nucleus/tail of the VTA (RMTg/tVTA) and on the VT...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506920/ https://www.ncbi.nlm.nih.gov/pubmed/37474756 http://dx.doi.org/10.1007/s00213-023-06425-4 |
_version_ | 1785107205023858688 |
---|---|
author | Esposito-Zapero, Claudia Fernández-Rodríguez, Sandra Sánchez-Catalán, María José Zornoza, Teodoro Cano-Cebrián, María José Granero, Luis |
author_facet | Esposito-Zapero, Claudia Fernández-Rodríguez, Sandra Sánchez-Catalán, María José Zornoza, Teodoro Cano-Cebrián, María José Granero, Luis |
author_sort | Esposito-Zapero, Claudia |
collection | PubMed |
description | RATIONALE: Opioid drugs indirectly activate dopamine (DA) neurons in the ventral tegmental area (VTA) through a disinhibition mechanism mediated by mu opioid receptors (MORs) present both on the GABA projection neurons located in the medial tegmental nucleus/tail of the VTA (RMTg/tVTA) and on the VTA GABA interneurons. It is well demonstrated that ethanol, like opioid drugs, provokes VTA DA neuron disinhibition by interacting (through its secondary metabolite, salsolinol) with MORs present in VTA GABA interneurons, but it is not known whether ethanol could disinhibit VTA DA neurons through the MORs present in the RMTg/tVTA. OBJECTIVES: The objective of the present study was to determine whether ethanol, directly microinjected into the tVTA/RMTg, is also able to induce VTA DA neurons disinhibition. METHODS: Disinhibition of VTA DA neurons was indirectly assessed through the analysis of the motor activity of rats. Cannulae were placed into the tVTA/RMTg to perform microinjections of DAMGO (0.13 nmol), ethanol (150 or 300 nmol) or acetaldehyde (250 nmol) in animals pre-treated with either aCSF or the irreversible antagonist of MORs, beta-funaltrexamine (beta-FNA; 2.5 nmol). After injections, spontaneous activity was monitored for 30 min. RESULTS: Neither ethanol nor acetaldehyde directly administered into the RMTg/tVTA were able to increase the locomotor activity of rats at doses that, in previous studies performed in the posterior VTA, were effective in increasing motor activities. However, microinjections of 0.13 nmol of DAMGO into the tVTA/RMTg significantly increased the locomotor activity of rats. These activating effects were reduced by local pre-treatment of rats with beta-FNA (2.5 nmol). CONCLUSIONS: The tVTA/RMTg does not appear to be a key brain region for the disinhibiting action of ethanol on VTA DA neurons. The absence of dopamine in the tVTA/RMTg extracellular medium, the lack of local ethanol metabolism or both could explain the present results. |
format | Online Article Text |
id | pubmed-10506920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-105069202023-09-20 The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats Esposito-Zapero, Claudia Fernández-Rodríguez, Sandra Sánchez-Catalán, María José Zornoza, Teodoro Cano-Cebrián, María José Granero, Luis Psychopharmacology (Berl) Original Investigation RATIONALE: Opioid drugs indirectly activate dopamine (DA) neurons in the ventral tegmental area (VTA) through a disinhibition mechanism mediated by mu opioid receptors (MORs) present both on the GABA projection neurons located in the medial tegmental nucleus/tail of the VTA (RMTg/tVTA) and on the VTA GABA interneurons. It is well demonstrated that ethanol, like opioid drugs, provokes VTA DA neuron disinhibition by interacting (through its secondary metabolite, salsolinol) with MORs present in VTA GABA interneurons, but it is not known whether ethanol could disinhibit VTA DA neurons through the MORs present in the RMTg/tVTA. OBJECTIVES: The objective of the present study was to determine whether ethanol, directly microinjected into the tVTA/RMTg, is also able to induce VTA DA neurons disinhibition. METHODS: Disinhibition of VTA DA neurons was indirectly assessed through the analysis of the motor activity of rats. Cannulae were placed into the tVTA/RMTg to perform microinjections of DAMGO (0.13 nmol), ethanol (150 or 300 nmol) or acetaldehyde (250 nmol) in animals pre-treated with either aCSF or the irreversible antagonist of MORs, beta-funaltrexamine (beta-FNA; 2.5 nmol). After injections, spontaneous activity was monitored for 30 min. RESULTS: Neither ethanol nor acetaldehyde directly administered into the RMTg/tVTA were able to increase the locomotor activity of rats at doses that, in previous studies performed in the posterior VTA, were effective in increasing motor activities. However, microinjections of 0.13 nmol of DAMGO into the tVTA/RMTg significantly increased the locomotor activity of rats. These activating effects were reduced by local pre-treatment of rats with beta-FNA (2.5 nmol). CONCLUSIONS: The tVTA/RMTg does not appear to be a key brain region for the disinhibiting action of ethanol on VTA DA neurons. The absence of dopamine in the tVTA/RMTg extracellular medium, the lack of local ethanol metabolism or both could explain the present results. Springer Berlin Heidelberg 2023-07-20 2023 /pmc/articles/PMC10506920/ /pubmed/37474756 http://dx.doi.org/10.1007/s00213-023-06425-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Investigation Esposito-Zapero, Claudia Fernández-Rodríguez, Sandra Sánchez-Catalán, María José Zornoza, Teodoro Cano-Cebrián, María José Granero, Luis The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats |
title | The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats |
title_full | The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats |
title_fullStr | The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats |
title_full_unstemmed | The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats |
title_short | The rostromedial tegmental nucleus RMTg is not a critical site for ethanol-induced motor activation in rats |
title_sort | rostromedial tegmental nucleus rmtg is not a critical site for ethanol-induced motor activation in rats |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506920/ https://www.ncbi.nlm.nih.gov/pubmed/37474756 http://dx.doi.org/10.1007/s00213-023-06425-4 |
work_keys_str_mv | AT espositozaperoclaudia therostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT fernandezrodriguezsandra therostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT sanchezcatalanmariajose therostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT zornozateodoro therostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT canocebrianmariajose therostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT graneroluis therostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT espositozaperoclaudia rostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT fernandezrodriguezsandra rostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT sanchezcatalanmariajose rostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT zornozateodoro rostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT canocebrianmariajose rostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats AT graneroluis rostromedialtegmentalnucleusrmtgisnotacriticalsiteforethanolinducedmotoractivationinrats |