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The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission

Dopamine neurotransmission is highly dysregulated by the psychostimulant methamphetamine, a substrate for the dopamine transporter (DAT). Through interactions with DAT, methamphetamine increases extracellular dopamine levels in the brain, leading to its rewarding and addictive properties. Methamphet...

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Autores principales: Sambo, Danielle O., Lin, Min, Owens, Anthony, Lebowitz, Joseph J., Richardson, Ben, Jagnarine, Darin A., Shetty, Madhur, Rodriquez, Meghan, Alonge, Taiwo, Ali, Mishaal, Katz, Jonathan, Yan, Long, Febo, Marcelo, Henry, L. Keith, Bruijnzeel, Adriaan W., Daws, Lynette, Khoshbouei, Habibeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738444/
https://www.ncbi.nlm.nih.gov/pubmed/29263318
http://dx.doi.org/10.1038/s41467-017-02087-x
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author Sambo, Danielle O.
Lin, Min
Owens, Anthony
Lebowitz, Joseph J.
Richardson, Ben
Jagnarine, Darin A.
Shetty, Madhur
Rodriquez, Meghan
Alonge, Taiwo
Ali, Mishaal
Katz, Jonathan
Yan, Long
Febo, Marcelo
Henry, L. Keith
Bruijnzeel, Adriaan W.
Daws, Lynette
Khoshbouei, Habibeh
author_facet Sambo, Danielle O.
Lin, Min
Owens, Anthony
Lebowitz, Joseph J.
Richardson, Ben
Jagnarine, Darin A.
Shetty, Madhur
Rodriquez, Meghan
Alonge, Taiwo
Ali, Mishaal
Katz, Jonathan
Yan, Long
Febo, Marcelo
Henry, L. Keith
Bruijnzeel, Adriaan W.
Daws, Lynette
Khoshbouei, Habibeh
author_sort Sambo, Danielle O.
collection PubMed
description Dopamine neurotransmission is highly dysregulated by the psychostimulant methamphetamine, a substrate for the dopamine transporter (DAT). Through interactions with DAT, methamphetamine increases extracellular dopamine levels in the brain, leading to its rewarding and addictive properties. Methamphetamine also interacts with the sigma-1 receptor (σ(1)R), an inter-organelle signaling modulator. Using complementary strategies, we identified a novel mechanism for σ(1)R regulation of dopamine neurotransmission in response to methamphetamine. We found that σ(1)R activation prevents methamphetamine-induced, DAT-mediated increases in firing activity of dopamine neurons. In vitro and in vivo amperometric measurements revealed that σ(1)R activation decreases methamphetamine-stimulated dopamine efflux without affecting basal dopamine neurotransmission. Consistent with these findings, σ(1)R activation decreases methamphetamine-induced locomotion, motivated behavior, and enhancement of brain reward function. Notably, we revealed that the σ(1)R interacts with DAT at or near the plasma membrane and decreases methamphetamine-induced Ca(2+) signaling, providing potential mechanisms. Broadly, these data provide evidence for σ(1)R regulation of dopamine neurotransmission and support the σ(1)R as a putative target for the treatment of methamphetamine addiction.
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spelling pubmed-57384442017-12-22 The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission Sambo, Danielle O. Lin, Min Owens, Anthony Lebowitz, Joseph J. Richardson, Ben Jagnarine, Darin A. Shetty, Madhur Rodriquez, Meghan Alonge, Taiwo Ali, Mishaal Katz, Jonathan Yan, Long Febo, Marcelo Henry, L. Keith Bruijnzeel, Adriaan W. Daws, Lynette Khoshbouei, Habibeh Nat Commun Article Dopamine neurotransmission is highly dysregulated by the psychostimulant methamphetamine, a substrate for the dopamine transporter (DAT). Through interactions with DAT, methamphetamine increases extracellular dopamine levels in the brain, leading to its rewarding and addictive properties. Methamphetamine also interacts with the sigma-1 receptor (σ(1)R), an inter-organelle signaling modulator. Using complementary strategies, we identified a novel mechanism for σ(1)R regulation of dopamine neurotransmission in response to methamphetamine. We found that σ(1)R activation prevents methamphetamine-induced, DAT-mediated increases in firing activity of dopamine neurons. In vitro and in vivo amperometric measurements revealed that σ(1)R activation decreases methamphetamine-stimulated dopamine efflux without affecting basal dopamine neurotransmission. Consistent with these findings, σ(1)R activation decreases methamphetamine-induced locomotion, motivated behavior, and enhancement of brain reward function. Notably, we revealed that the σ(1)R interacts with DAT at or near the plasma membrane and decreases methamphetamine-induced Ca(2+) signaling, providing potential mechanisms. Broadly, these data provide evidence for σ(1)R regulation of dopamine neurotransmission and support the σ(1)R as a putative target for the treatment of methamphetamine addiction. Nature Publishing Group UK 2017-12-20 /pmc/articles/PMC5738444/ /pubmed/29263318 http://dx.doi.org/10.1038/s41467-017-02087-x Text en © The Author(s) 2017 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 Commonslicense, unless indicated otherwise in a credit line to the material. If material is not included in the article’sCreative 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/.
spellingShingle Article
Sambo, Danielle O.
Lin, Min
Owens, Anthony
Lebowitz, Joseph J.
Richardson, Ben
Jagnarine, Darin A.
Shetty, Madhur
Rodriquez, Meghan
Alonge, Taiwo
Ali, Mishaal
Katz, Jonathan
Yan, Long
Febo, Marcelo
Henry, L. Keith
Bruijnzeel, Adriaan W.
Daws, Lynette
Khoshbouei, Habibeh
The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
title The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
title_full The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
title_fullStr The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
title_full_unstemmed The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
title_short The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
title_sort sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738444/
https://www.ncbi.nlm.nih.gov/pubmed/29263318
http://dx.doi.org/10.1038/s41467-017-02087-x
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