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Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?

The adenosine A(2A) receptor is a major target of caffeine, the most widely used psychoactive substance worldwide. Large epidemiological studies have long shown caffeine consumption is a strong inverse predictor of Parkinson’s disease (PD). In this review, we first examine the epidemiology of caffei...

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Detalles Bibliográficos
Autores principales: Chen, Jiang-Fan, Schwarzschild, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102090/
https://www.ncbi.nlm.nih.gov/pubmed/33349580
http://dx.doi.org/10.1016/j.parkreldis.2020.10.024
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author Chen, Jiang-Fan
Schwarzschild, Michael A.
author_facet Chen, Jiang-Fan
Schwarzschild, Michael A.
author_sort Chen, Jiang-Fan
collection PubMed
description The adenosine A(2A) receptor is a major target of caffeine, the most widely used psychoactive substance worldwide. Large epidemiological studies have long shown caffeine consumption is a strong inverse predictor of Parkinson’s disease (PD). In this review, we first examine the epidemiology of caffeine use vis-à-vis PD and follow this by looking at the evidence for adenosine A(2A) receptor antagonists as potential neuroprotective agents. There is a wealth of accumulating biological, epidemiological and clinical evidence to support the further investigation of selective adenosine A(2A) antagonists, as well as caffeine, as promising candidate therapeutics to fill the unmet need for disease modification of PD.
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spelling pubmed-81020902021-12-19 Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease? Chen, Jiang-Fan Schwarzschild, Michael A. Parkinsonism Relat Disord Article The adenosine A(2A) receptor is a major target of caffeine, the most widely used psychoactive substance worldwide. Large epidemiological studies have long shown caffeine consumption is a strong inverse predictor of Parkinson’s disease (PD). In this review, we first examine the epidemiology of caffeine use vis-à-vis PD and follow this by looking at the evidence for adenosine A(2A) receptor antagonists as potential neuroprotective agents. There is a wealth of accumulating biological, epidemiological and clinical evidence to support the further investigation of selective adenosine A(2A) antagonists, as well as caffeine, as promising candidate therapeutics to fill the unmet need for disease modification of PD. 2020-12-19 2020-11 /pmc/articles/PMC8102090/ /pubmed/33349580 http://dx.doi.org/10.1016/j.parkreldis.2020.10.024 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Chen, Jiang-Fan
Schwarzschild, Michael A.
Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?
title Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?
title_full Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?
title_fullStr Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?
title_full_unstemmed Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?
title_short Do caffeine and more selective adenosine A(2A) receptor antagonists protect against dopaminergic neurodegeneration in Parkinson’s disease?
title_sort do caffeine and more selective adenosine a(2a) receptor antagonists protect against dopaminergic neurodegeneration in parkinson’s disease?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102090/
https://www.ncbi.nlm.nih.gov/pubmed/33349580
http://dx.doi.org/10.1016/j.parkreldis.2020.10.024
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