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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International Scientific Literature, Inc.
2012
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560700/ |
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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/ |
_version_ |
1611951524821336064 |