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Impairment of Serotonergic Transmission by the Antiparkinsonian Drug L-DOPA: Mechanisms and Clinical Implications.
Miguelez, Cristina; Benazzouz, Abdelhamid; Ugedo, Luisa; De Deurwaerdère, Philippe.
Afiliación
  • Miguelez C; Department of Pharmacology, Faculty of Medicine and Dentistry, University of the Basque Country (UPV/EHU)Leioa, Spain.
  • Benazzouz A; Institut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293Bordeaux, France.
  • Ugedo L; CNRS, Institut des Maladies Neurodégénératives, UMR 5293Bordeaux, France.
  • De Deurwaerdère P; Department of Pharmacology, Faculty of Medicine and Dentistry, University of the Basque Country (UPV/EHU)Leioa, Spain.
Front Cell Neurosci ; 11: 274, 2017.
Article en En | MEDLINE | ID: mdl-28955204
The 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Neurosci Año: 2017 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Neurosci Año: 2017 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza