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Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse
Concurrent cocaine and alcohol use is among the most frequent drug combination, and among the most dangerous in terms of deleterious outcomes. Cocaine increases extracellular monoamines by blocking dopamine (DA), norepinephrine (NE) and serotonin (5-HT) transporters (DAT, NET and SERT, respectively)...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615754/ https://www.ncbi.nlm.nih.gov/pubmed/37308680 http://dx.doi.org/10.1038/s41380-023-02064-5 |
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author | Clauss, N. J. Mayer, F. P. Owens, W. A. Vitela, M. Clarke, K. M. Bowman, M. A. Horton, R. E. Gründemann, D. Schmid, D. Holy, M. Gould, G. G. Koek, W. Sitte, H. H. Daws, L. C. |
author_facet | Clauss, N. J. Mayer, F. P. Owens, W. A. Vitela, M. Clarke, K. M. Bowman, M. A. Horton, R. E. Gründemann, D. Schmid, D. Holy, M. Gould, G. G. Koek, W. Sitte, H. H. Daws, L. C. |
author_sort | Clauss, N. J. |
collection | PubMed |
description | Concurrent cocaine and alcohol use is among the most frequent drug combination, and among the most dangerous in terms of deleterious outcomes. Cocaine increases extracellular monoamines by blocking dopamine (DA), norepinephrine (NE) and serotonin (5-HT) transporters (DAT, NET and SERT, respectively). Likewise, ethanol also increases extracellular monoamines, however evidence suggests that ethanol does so independently of DAT, NET and SERT. Organic cation transporter 3 (OCT3) is an emergent key player in the regulation of monoamine signaling. Using a battery of in vitro, in vivo electrochemical, and behavioral approaches, as well as wild-type and constitutive OCT3 knockout mice, we show that ethanol’s actions to inhibit monoamine uptake are dependent on OCT3. These findings provide a novel mechanistic basis whereby ethanol enhances the neurochemical and behavioral effects of cocaine and encourage further research into OCT3 as a target for therapeutic intervention in the treatment of ethanol and ethanol/cocaine use disorders. |
format | Online Article Text |
id | pubmed-10615754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106157542023-11-01 Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse Clauss, N. J. Mayer, F. P. Owens, W. A. Vitela, M. Clarke, K. M. Bowman, M. A. Horton, R. E. Gründemann, D. Schmid, D. Holy, M. Gould, G. G. Koek, W. Sitte, H. H. Daws, L. C. Mol Psychiatry Article Concurrent cocaine and alcohol use is among the most frequent drug combination, and among the most dangerous in terms of deleterious outcomes. Cocaine increases extracellular monoamines by blocking dopamine (DA), norepinephrine (NE) and serotonin (5-HT) transporters (DAT, NET and SERT, respectively). Likewise, ethanol also increases extracellular monoamines, however evidence suggests that ethanol does so independently of DAT, NET and SERT. Organic cation transporter 3 (OCT3) is an emergent key player in the regulation of monoamine signaling. Using a battery of in vitro, in vivo electrochemical, and behavioral approaches, as well as wild-type and constitutive OCT3 knockout mice, we show that ethanol’s actions to inhibit monoamine uptake are dependent on OCT3. These findings provide a novel mechanistic basis whereby ethanol enhances the neurochemical and behavioral effects of cocaine and encourage further research into OCT3 as a target for therapeutic intervention in the treatment of ethanol and ethanol/cocaine use disorders. Nature Publishing Group UK 2023-06-13 2023 /pmc/articles/PMC10615754/ /pubmed/37308680 http://dx.doi.org/10.1038/s41380-023-02064-5 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Clauss, N. J. Mayer, F. P. Owens, W. A. Vitela, M. Clarke, K. M. Bowman, M. A. Horton, R. E. Gründemann, D. Schmid, D. Holy, M. Gould, G. G. Koek, W. Sitte, H. H. Daws, L. C. Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse |
title | Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse |
title_full | Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse |
title_fullStr | Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse |
title_full_unstemmed | Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse |
title_short | Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse |
title_sort | ethanol inhibits dopamine uptake via organic cation transporter 3: implications for ethanol and cocaine co-abuse |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615754/ https://www.ncbi.nlm.nih.gov/pubmed/37308680 http://dx.doi.org/10.1038/s41380-023-02064-5 |
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