http://www.cnr.it/ontology/cnr/individuo/prodotto/ID37799
New therapies for the treatment of Parkinson's disease: adenosine A2A receptor antagonists (Articolo in rivista)
- Type
- Label
- New therapies for the treatment of Parkinson's disease: adenosine A2A receptor antagonists (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.lfs.2005.04.029 (literal)
- Alternative label
Pinna A., Wardas J., Simola N., Morelli M (2005)
New therapies for the treatment of Parkinson's disease: adenosine A2A receptor antagonists
in Life sciences (1973)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Pinna A., Wardas J., Simola N., Morelli M (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- CNR Institute of Neuroscience-Cagliari section, Italy
Department of Toxicology, University of Cagliari, Palazzo delle Scienze, via Ospedale 72, 09124 Cagliari, Italy
Department of Neuropsychopharmacology, Institute of Pharmacology, Polish Academy of Sciences, 12 Smetna St., 31-343 Krakow, PolandCNR (literal)
- Titolo
- New therapies for the treatment of Parkinson's disease: adenosine A2A receptor antagonists (literal)
- Abstract
- The development of non-dopaminergic therapies for the treatment of Parkinson's disease (PD) has attracted much interest in recent years. Among new different classes of drugs, adenosine A(2A) receptor antagonists have emerged as best candidates. The present review will provide an updated summary of the results reported in literature concerning the effects of adenosine A(2A) antagonists in rodent and primate models of PD. These results show that A(2A) receptor antagonists improve motor deficits without inducing dyskinesia and counteract parkinsonian tremor. In progress clinical trials have shown that a low dose of L-DOPA plus KW-6002 produced symptomatic relief no different from that produced by an optimal dose of L-DOPA alone, whereas dyskinesias were reduced rendering this class of compounds particularly attractive. (c) 2005 Elsevier Inc. All rights reserved. (literal)
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