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Role of adenosine A(2A) receptors in motor control: relevance to Parkinson's disease and dyskinesia

Articolo
Data di Pubblicazione:
2018
Abstract:
Adenosine is an endogenous purine nucleoside that regulates several physiological functions, at the central and peripheral levels. Besides, adenosine has emerged as a major player in the regulation of motor behavior. In fact, adenosine receptors of the A(2A) subtype are highly enriched in the caudate-putamen, which is richly innervated by dopamine. Moreover, several studies in experimental animals have consistently demonstrated that the pharmacological antagonism of A(2A) receptors has a facilitatory influence on motor behavior. Taken together, these findings have envisaged A(2A) receptors as a promising target for symptomatic therapies aimed at ameliorating motor deficits. Accordingly, A(2A) receptor antagonists have been extensively studied as new agents for the treatment of Parkinson's disease (PD), the epitome of motor disorders. In this review, we provide an overview of the effects that adenosine A(2A) receptor antagonists elicit in rodent and primate experimental models of PD, with regard to the counteraction of motor deficits as well as to manifestation of dyskinesia and motor fluctuations. Moreover, we briefly present the results of clinical trials of A(2A) receptor antagonists in PD patients experiencing motor fluctuations, with particular regard to dyskinesia. Finally, we discuss the interaction between A(2A) receptor antagonists and serotonin receptor agonists, since combined administration of these drugs has recently emerged as a new potential therapeutic strategy in the treatment of dyskinesia.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Basal ganglia; Caudate-putamen; Clinical trial; Primate; Rodent; Serotonin
Elenco autori:
Morelli, Micaela; Pinna, Annalisa
Autori di Ateneo:
PINNA ANNALISA
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/351221
Pubblicato in:
JOURNAL OF NEURAL TRANSMISSION
Journal
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URL

https://www.ncbi.nlm.nih.gov/pubmed/29396609
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