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Opioid system in L-DOPA-induced dyskinesia

L-3, 4-Dihydroxyphenylalanine (L-DOPA)-induced dyskinesia (LID) is a major clinical complication in the treatment of Parkinson’s disease (PD). This debilitating side effect likely reflects aberrant compensatory responses for a combination of dopaminergic neuron denervation and repeated L-DOPA admini...

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Detalles Bibliográficos
Autores principales: Pan, Jing, Cai, Huaibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240307/
https://www.ncbi.nlm.nih.gov/pubmed/28105331
http://dx.doi.org/10.1186/s40035-017-0071-y
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author Pan, Jing
Cai, Huaibin
author_facet Pan, Jing
Cai, Huaibin
author_sort Pan, Jing
collection PubMed
description L-3, 4-Dihydroxyphenylalanine (L-DOPA)-induced dyskinesia (LID) is a major clinical complication in the treatment of Parkinson’s disease (PD). This debilitating side effect likely reflects aberrant compensatory responses for a combination of dopaminergic neuron denervation and repeated L-DOPA administration. Abnormal endogenous opioid signal transduction pathways in basal ganglia have been well documented in LID. Opioid receptors have been targeted to alleviate the dyskinesia. However, the exact role of this altered opioid activity is remains under active investigation. In the present review, we discuss the current understanding of opioid signal transduction in the basal ganglia and how the malfunction of opioid signaling contributes to the pathophysiology of LID. Further study of the opioid system in LID may lead to new therapeutic targets and improved treatment of PD patients.
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spelling pubmed-52403072017-01-19 Opioid system in L-DOPA-induced dyskinesia Pan, Jing Cai, Huaibin Transl Neurodegener Review L-3, 4-Dihydroxyphenylalanine (L-DOPA)-induced dyskinesia (LID) is a major clinical complication in the treatment of Parkinson’s disease (PD). This debilitating side effect likely reflects aberrant compensatory responses for a combination of dopaminergic neuron denervation and repeated L-DOPA administration. Abnormal endogenous opioid signal transduction pathways in basal ganglia have been well documented in LID. Opioid receptors have been targeted to alleviate the dyskinesia. However, the exact role of this altered opioid activity is remains under active investigation. In the present review, we discuss the current understanding of opioid signal transduction in the basal ganglia and how the malfunction of opioid signaling contributes to the pathophysiology of LID. Further study of the opioid system in LID may lead to new therapeutic targets and improved treatment of PD patients. BioMed Central 2017-01-17 /pmc/articles/PMC5240307/ /pubmed/28105331 http://dx.doi.org/10.1186/s40035-017-0071-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Pan, Jing
Cai, Huaibin
Opioid system in L-DOPA-induced dyskinesia
title Opioid system in L-DOPA-induced dyskinesia
title_full Opioid system in L-DOPA-induced dyskinesia
title_fullStr Opioid system in L-DOPA-induced dyskinesia
title_full_unstemmed Opioid system in L-DOPA-induced dyskinesia
title_short Opioid system in L-DOPA-induced dyskinesia
title_sort opioid system in l-dopa-induced dyskinesia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240307/
https://www.ncbi.nlm.nih.gov/pubmed/28105331
http://dx.doi.org/10.1186/s40035-017-0071-y
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