Positron emission tomography analysis of [11C]KW-6002 binding to human and rat adenosine A2A receptors in the brain
Article first published online: 19 JUN 2008
Copyright © 2008 Wiley-Liss, Inc.
Volume 62, Issue 9, pages 671–681, September 2008
How to Cite
Brooks, D.J., Doder, M., Osman, S., Luthra, S.K., Hirani, E., Hume, S., Kase, H., Kilborn, J., Martindill, S. and Mori, A. (2008), Positron emission tomography analysis of [11C]KW-6002 binding to human and rat adenosine A2A receptors in the brain. Synapse, 62: 671–681. doi: 10.1002/syn.20539
- Issue published online: 24 JUN 2008
- Article first published online: 19 JUN 2008
- Manuscript Accepted: 26 FEB 2008
- Manuscript Revised: 9 FEB 2008
- Manuscript Received: 10 OCT 2006
- kinetic modeling;
- positron emission tomography (PET);
- receptor occupancy
Adenosine A2A receptors are found on striatal neurones projecting to the external pallidum. KW-6002 (istradefylline) is a potent and selective antagonist for the adenosine A2A receptors in the CNS and acts to inhibit the excessive activity of this pathway in the MPTP marmoset model of PD, thus relieving parkinsonism. The objectives of this study were to investigate the regional binding of the novel positron emission tomography tracer [11C]KW-6002 in the healthy human brain and the rat brain, along with receptor occupancy by cold KW-6002 at varying doses in human. The highest [11C]KW-6002 uptake in the rat brain was seen in striatum and lower levels in cortex and cerebellum. Brain [11C]KW-6002 uptake was well characterized in humans by a two-tissue compartmental model with a blood volume term, and the ED50 of cold KW-6002 was 0.5 mg in the striatum. Over 90% receptor occupancy was achieved with daily oral doses of greater than 5 mg. In humans, blockable binding was present in all gray matter structures including the cerebellum, which has not been reported to express A2A receptors. MRS 1745, an A2B receptor selective antagonist, had no effect on the cerebellar binding of [11C]KW-6002 in rats, suggesting that this blockable signal is unlikely to result from an affinity for adenosine A2B receptors. Synapse 62:671–681, 2008. © 2008 Wiley-Liss, Inc.