Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit

Clinical observations stemming from widespread employment of restorative L-3,4-dihydroxyphenylalanine (L-DOPA) therapy for management of dyskinesia in Parkinson’s Disease (PD) patients implicate a regulatory role for endogenous morphine in central nervous system dopamine neurotransmission. Reciproca...

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Main Authors: Stefano, George B., Mantione, Kirk J., Králíčková, Milena, Ptacek, Radek, Kuzelova, Hana, Esch, Tobias, Kream, Richard M.
Format: Online
Language:English
Published: International Scientific Literature, Inc. 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560700/
id pubmed-3560700
recordtype oai_dc
spelling pubmed-35607002013-04-24 Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit Stefano, George B. Mantione, Kirk J. Králíčková, Milena Ptacek, Radek Kuzelova, Hana Esch, Tobias Kream, Richard M. Review Article Clinical observations stemming from widespread employment of restorative L-3,4-dihydroxyphenylalanine (L-DOPA) therapy for management of dyskinesia in Parkinson’s Disease (PD) patients implicate a regulatory role for endogenous morphine in central nervous system dopamine neurotransmission. Reciprocally, it appears that restorative L-DOPA administration has provided us with a compelling in vivo pharmacological model for targeting peripheral sites involved in endogenous morphine expression in human subjects. The biological activities underlying endogenous morphine expression and its interaction with its major precursor dopamine strongly suggest that endogenous morphine systems are reciprocally dysregulated in PD. These critical issues are examined from historical and current perspectives within our short review. International Scientific Literature, Inc. 2012-08-01 /pmc/articles/PMC3560700/ /pubmed/22847214 http://dx.doi.org/10.12659/MSM.883259 Text en © Med Sci Monit, 2012 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Stefano, George B.
Mantione, Kirk J.
Králíčková, Milena
Ptacek, Radek
Kuzelova, Hana
Esch, Tobias
Kream, Richard M.
spellingShingle Stefano, George B.
Mantione, Kirk J.
Králíčková, Milena
Ptacek, Radek
Kuzelova, Hana
Esch, Tobias
Kream, Richard M.
Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit
author_facet Stefano, George B.
Mantione, Kirk J.
Králíčková, Milena
Ptacek, Radek
Kuzelova, Hana
Esch, Tobias
Kream, Richard M.
author_sort Stefano, George B.
title Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit
title_short Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit
title_full Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit
title_fullStr Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit
title_full_unstemmed Parkinson’s disease, L-DOPA, and endogenous morphine: A revisit
title_sort parkinson’s disease, l-dopa, and endogenous morphine: a revisit
description Clinical observations stemming from widespread employment of restorative L-3,4-dihydroxyphenylalanine (L-DOPA) therapy for management of dyskinesia in Parkinson’s Disease (PD) patients implicate a regulatory role for endogenous morphine in central nervous system dopamine neurotransmission. Reciprocally, it appears that restorative L-DOPA administration has provided us with a compelling in vivo pharmacological model for targeting peripheral sites involved in endogenous morphine expression in human subjects. The biological activities underlying endogenous morphine expression and its interaction with its major precursor dopamine strongly suggest that endogenous morphine systems are reciprocally dysregulated in PD. These critical issues are examined from historical and current perspectives within our short review.
publisher International Scientific Literature, Inc.
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560700/
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