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dc.contributor.authorMiguélez Palomo, Cristina
dc.contributor.authorBenazzouz, Abdelhamid
dc.contributor.authorUgedo Urruela, Luisa
dc.contributor.authorDe Deurwaerdère, Philippe
dc.date.accessioned2018-06-14T11:42:51Z
dc.date.available2018-06-14T11:42:51Z
dc.date.issued2017-09-12
dc.identifier.citationFrontiers in Cellular Neuroscience 11 : (2017) // Article ID 274es_ES
dc.identifier.issn1662-5102
dc.identifier.urihttp://hdl.handle.net/10810/27524
dc.description.abstractThe link between the anti-Parkinsonian drug L-3,4-dihydroxyphenylalanine (L-DOPA) and the serotonergic (5-HT) system has been long established and has received increased attention during the last decade. Most studies have focused on the fact that L-DOPA can be transformed into dopamine (DA) and released from 5-HT terminals, which is especially important for the management of L-DOPA-induced dyskinesia. In patients, treatment using L-DOPA also impacts 5-HT neurotransmission; however, few studies have investigated the mechanisms of this effect. The purpose of this review is to summarize the electrophysiological and neurochemical data concerning the effects of L-DOPA on 5-HT cell function. This review will argue that L-DOPA disrupts the link between the electrical activity of 5-HT neurons and 5-HT release as well as that between 5-HT release and extracellular 5-HT levels. These effects are caused by the actions of L-DOPA and DA in 5-HT neurons, which affect 5-HT neurotransmission from the biosynthesis of 5-HT to the impairment of the 5-HT transporter. The interaction between L-DOPA and 5-HT transmission is especially relevant in those Parkinson's disease (PD) patients that suffer dyskinesia, comorbid anxiety or depression, since the efficacy of antidepressants or 5-HT compounds may be affected.es_ES
dc.description.sponsorshipThe project was funded by grants from the Government of the Basque Country (IT 747-13), the Spanish Government [SAF2016-77758-R (AEI/FEDER, UE)] and by the Fondation de France. PDD acknowledges the support given by the cooperation for science and technology (COST) action CM15120. PDD and AB acknowledge the support of the Centre National de la Recherche Scientifique.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectserotonines_ES
dc.subjectdopaminees_ES
dc.subjectelectrophysiologyes_ES
dc.subjectintracerebral microdialysises_ES
dc.subjectdepressiones_ES
dc.subjectdyskinesiaes_ES
dc.subjectParkinson's diseasees_ES
dc.subjectexocytosises_ES
dc.subjectdorsal raphe nucleuses_ES
dc.subjectlevodopa-induced dyskinesiases_ES
dc.subjecthigh-frequency stimulationes_ES
dc.subject5-ht4 receptors exertes_ES
dc.subjectin-vivoes_ES
dc.subjectextracellular dopaminees_ES
dc.subjectrat modeles_ES
dc.subject6-hydroxydopamine-treated ratses_ES
dc.subjectnigrostriatal denervationes_ES
dc.titleImpairment of Serotonergic Transmission by the Antiparkinsonian Drug L-DOPA: Mechanisms and Clinical Implicationses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder2017 Miguelez, Benazzouz, Ugedo and De Deurwaerdère. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fncel.2017.00274/fulles_ES
dc.identifier.doi10.3389/fncel.2017.00274
dc.departamentoesFarmacologíaes_ES
dc.departamentoeuFarmakologiaes_ES


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2017 Miguelez, Benazzouz, Ugedo and De Deurwaerdère. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's license is described as 2017 Miguelez, Benazzouz, Ugedo and De Deurwaerdère. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.