Brain Advance Access published online on March 19, 2004
Brain, doi:10.1093/brain/awh128
© 2004 by Guarantors of Brain
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Article
1 Molecular Endocrinology and Oncology Research Center, Laval University Medical Center (CHUL) and Faculty of Pharmacy, Laval University, Québec, Canada
* Corresponding author. E-mail: therese.dipaolo{at}crchul.ulaval.ca.
Received 8 August 2003
; revised 19 December 2003
; accepted 22 December 2003
Brain adenosine A2A receptors have recently attracted considerable attention because of their interaction with the dopaminergic system and as potential targets for Parkinsons disease pharmacotherapy. Post mortem adenosine A2A receptor mRNA and [3H]SCH 58261- specific binding to adenosine A2A receptor were studied in the brain of Parkinsons disease patients using in situ hybridization and receptor binding autoradiography, respectively. Fourteen levodopa-treated Parkinsons disease patients, of which seven developed dyskinesias and seven did not, were compared with nine controls. Nigrostriatal denervation was similar between dyskinetic and non-dyskinetic Parkinsons disease patients, as assessed with catecholamine concentrations and [125I]RTI-121-specific binding to dopamine transporters. A2A receptor mRNA levels (+129%; P < 0.01) and [3H]SCH 58261-specific binding (+32%, P < 0.01) were increased in the putamen (lateral and medial) of dyskinetic patients compared with controls. The increase of adenosine A2A receptor mRNA in dyskinetic Parkinsons disease patients was also significant compared with non-dyskinetic Parkinsons disease patients (+60%; P < 0.05) in the lateral putamen. Moreover, [3H]SCH 58261-specific binding to adenosine A2A receptors was increased in the external globus pallidus (+24%; P < 0.001) of Parkinsons disease patients compared with controls, regardless of the dyskinesigenic response to levodopa. No change of adenosine A2A receptors was observed in the caudate nucleus, whereas adenosine A2A receptor protein and mRNA levels in the internal globus pallidus were not different from background. These findings suggest that increased synthesis of adenosine A2A receptors in striatopallidal pathway neurons is associated with the development of dyskinesias following long-term levodopa therapy in Parkinsons disease.
Keywords: adenosine A2A receptors; motor complications; Parkinson’s disease; putamen; SCH 58261
Increased adenosine A2A receptors in the brain of Parkinsons disease patients with dyskinesias
2 Division of Neurology, University of Saskatchewan, Royal University Hospital, Saskatoon, Canada; Institute for Brain Research, Faculty of Medicine, University of Vienna, Vienna, Austria
3 Neuroscience Research Unit, Laval University Medical Center (CHUL) and Department of Medicine, Laval University, Québec, Canada
4 Division of Neurology, University of Saskatchewan, Royal University Hospital, Saskatoon, Canada
5 Molecular Endocrinology and Oncology Research Center, Laval University Medical Center (CHUL), 2705 Boul Laurier, Ste-Foy, Québec, Canada G1V 4G2
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
R. A. Hodgson, R. Bertorelli, G. B. Varty, J. E. Lachowicz, A. Forlani, S. Fredduzzi, M. E. Cohen-Williams, G. A. Higgins, F. Impagnatiello, E. Nicolussi, et al. Characterization of the Potent and Highly Selective A2A Receptor Antagonists Preladenant and SCH 412348 [7-[2-[4-2,4-Difluorophenyl]-1-piperazinyl]ethyl]-2-(2-furanyl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine] in Rodent Models of Movement Disorders and Depression J. Pharmacol. Exp. Ther., July 1, 2009; 330(1): 294 - 303. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Stacy, D. Silver, T. Mendis, J. Sutton, A. Mori, P. Chaikin, and N. M. Sussman A 12-week, placebo-controlled study (6002-US-006) of istradefylline in Parkinson disease Neurology, June 3, 2008; 70(23): 2233 - 2240. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. E. Benarroch Adenosine and its receptors: Multiple modulatory functions and potential therapeutic targets for neurologic disease Neurology, January 15, 2008; 70(3): 231 - 236. [Full Text] [PDF] |
||||
![]() |
G. Burnstock Physiology and Pathophysiology of Purinergic Neurotransmission Physiol Rev, April 1, 2007; 87(2): 659 - 797. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Linazasoro Pathophysiology of Motor Complications in Parkinson Disease: Postsynaptic Mechanisms Are Crucial Arch Neurol, January 1, 2007; 64(1): 137 - 140. [Full Text] [PDF] |
||||
![]() |
D. Xiao, E. Bastia, Y.-H. Xu, C. L. Benn, J.-H. J. Cha, T. S. Peterson, J.-F. Chen, and M. A. Schwarzschild Forebrain Adenosine A2A Receptors Contribute to L-3,4-Dihydroxyphenylalanine-Induced Dyskinesia in Hemiparkinsonian Mice J. Neurosci., December 27, 2006; 26(52): 13548 - 13555. [Abstract] [Full Text] [PDF] |
||||




