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Serotonin transport in the 21st century

Serotonin (5-hydroxytryptamine [5-HT]) is accumulated within nerve endings by the serotonin transporter (SERT), which terminates its extracellular action and provides cytoplasmic 5-HT for refilling of synaptic vesicles. SERT is the target for many antidepressant medications as well as psychostimulan...

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Detalles Bibliográficos
Autores principales: Rudnick, Gary, Sandtner, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829555/
https://www.ncbi.nlm.nih.gov/pubmed/31570504
http://dx.doi.org/10.1085/jgp.201812066
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author Rudnick, Gary
Sandtner, Walter
author_facet Rudnick, Gary
Sandtner, Walter
author_sort Rudnick, Gary
collection PubMed
description Serotonin (5-hydroxytryptamine [5-HT]) is accumulated within nerve endings by the serotonin transporter (SERT), which terminates its extracellular action and provides cytoplasmic 5-HT for refilling of synaptic vesicles. SERT is the target for many antidepressant medications as well as psychostimulants such as cocaine and ecstasy (3,4-methylenedioxymethamphetamine). SERT belongs to the SLC6 family of ion-coupled transporters and is structurally related to several other transporter families. SERT was studied in the 1970s and 1980s using membrane vesicles isolated from blood platelets. These studies led to a proposed stoichiometry of transport that has been challenged by high-resolution structures of SERT and its homologues and by studies of SERT electrophysiology. Here, we review the original evidence alongside more recent structural and electrophysiological evidence. A self-consistent picture emerges with surprising insights into the ion fluxes that accompany 5-HT transport.
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spelling pubmed-68295552020-05-04 Serotonin transport in the 21st century Rudnick, Gary Sandtner, Walter J Gen Physiol Reviews Serotonin (5-hydroxytryptamine [5-HT]) is accumulated within nerve endings by the serotonin transporter (SERT), which terminates its extracellular action and provides cytoplasmic 5-HT for refilling of synaptic vesicles. SERT is the target for many antidepressant medications as well as psychostimulants such as cocaine and ecstasy (3,4-methylenedioxymethamphetamine). SERT belongs to the SLC6 family of ion-coupled transporters and is structurally related to several other transporter families. SERT was studied in the 1970s and 1980s using membrane vesicles isolated from blood platelets. These studies led to a proposed stoichiometry of transport that has been challenged by high-resolution structures of SERT and its homologues and by studies of SERT electrophysiology. Here, we review the original evidence alongside more recent structural and electrophysiological evidence. A self-consistent picture emerges with surprising insights into the ion fluxes that accompany 5-HT transport. Rockefeller University Press 2019-11-04 2019-09-30 /pmc/articles/PMC6829555/ /pubmed/31570504 http://dx.doi.org/10.1085/jgp.201812066 Text en © 2019 Rudnick and Sandtner http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Reviews
Rudnick, Gary
Sandtner, Walter
Serotonin transport in the 21st century
title Serotonin transport in the 21st century
title_full Serotonin transport in the 21st century
title_fullStr Serotonin transport in the 21st century
title_full_unstemmed Serotonin transport in the 21st century
title_short Serotonin transport in the 21st century
title_sort serotonin transport in the 21st century
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829555/
https://www.ncbi.nlm.nih.gov/pubmed/31570504
http://dx.doi.org/10.1085/jgp.201812066
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