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Cocaine Modulates Locomotion Behavior in C. elegans

Cocaine, a potent addictive substance, is an inhibitor of monoamine transporters, including DAT (dopamine transporter), SERT (serotonin transporter) and NET (norepinephrine transporter). Cocaine administration induces complex behavioral alterations in mammals, but the underlying mechanisms are not w...

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Detalles Bibliográficos
Autores principales: Ward, Alex, Walker, Vyvyca J., Feng, Zhaoyang, Xu, X. Z. Shawn
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691951/
https://www.ncbi.nlm.nih.gov/pubmed/19536276
http://dx.doi.org/10.1371/journal.pone.0005946
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author Ward, Alex
Walker, Vyvyca J.
Feng, Zhaoyang
Xu, X. Z. Shawn
author_facet Ward, Alex
Walker, Vyvyca J.
Feng, Zhaoyang
Xu, X. Z. Shawn
author_sort Ward, Alex
collection PubMed
description Cocaine, a potent addictive substance, is an inhibitor of monoamine transporters, including DAT (dopamine transporter), SERT (serotonin transporter) and NET (norepinephrine transporter). Cocaine administration induces complex behavioral alterations in mammals, but the underlying mechanisms are not well understood. Here, we tested the effect of cocaine on C. elegans behavior. We show for the first time that acute cocaine treatment evokes changes in C. elegans locomotor activity. Interestingly, the neurotransmitter serotonin, rather than dopamine, is required for cocaine response in C. elegans. The C. elegans SERT MOD-5 is essential for the effect of cocaine, consistent with the role of cocaine in targeting monoamine transporters. We further show that the behavioral response to cocaine is primarily mediated by the ionotropic serotonin receptor MOD-1. Thus, cocaine modulates locomotion behavior in C. elegans primarily by impinging on its serotoninergic system.
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spelling pubmed-26919512009-06-16 Cocaine Modulates Locomotion Behavior in C. elegans Ward, Alex Walker, Vyvyca J. Feng, Zhaoyang Xu, X. Z. Shawn PLoS One Research Article Cocaine, a potent addictive substance, is an inhibitor of monoamine transporters, including DAT (dopamine transporter), SERT (serotonin transporter) and NET (norepinephrine transporter). Cocaine administration induces complex behavioral alterations in mammals, but the underlying mechanisms are not well understood. Here, we tested the effect of cocaine on C. elegans behavior. We show for the first time that acute cocaine treatment evokes changes in C. elegans locomotor activity. Interestingly, the neurotransmitter serotonin, rather than dopamine, is required for cocaine response in C. elegans. The C. elegans SERT MOD-5 is essential for the effect of cocaine, consistent with the role of cocaine in targeting monoamine transporters. We further show that the behavioral response to cocaine is primarily mediated by the ionotropic serotonin receptor MOD-1. Thus, cocaine modulates locomotion behavior in C. elegans primarily by impinging on its serotoninergic system. Public Library of Science 2009-06-17 /pmc/articles/PMC2691951/ /pubmed/19536276 http://dx.doi.org/10.1371/journal.pone.0005946 Text en Ward et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ward, Alex
Walker, Vyvyca J.
Feng, Zhaoyang
Xu, X. Z. Shawn
Cocaine Modulates Locomotion Behavior in C. elegans
title Cocaine Modulates Locomotion Behavior in C. elegans
title_full Cocaine Modulates Locomotion Behavior in C. elegans
title_fullStr Cocaine Modulates Locomotion Behavior in C. elegans
title_full_unstemmed Cocaine Modulates Locomotion Behavior in C. elegans
title_short Cocaine Modulates Locomotion Behavior in C. elegans
title_sort cocaine modulates locomotion behavior in c. elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691951/
https://www.ncbi.nlm.nih.gov/pubmed/19536276
http://dx.doi.org/10.1371/journal.pone.0005946
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