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Vol. 285, Issue 2, 561-567, May 1998
Department of Pharmacology and Therapeutics, University of Manitoba
Faculty of Medicine, Winnipeg, Manitoba, R3E 0T6, Canada
Glutamate release after ischemia, hypoxia and seizure activity plays an
important role in stimulating adenosine production and release. We
characterized the ionotropic glutamate receptor subtype that regulates
adenosine levels in vivo and investigated the role of
nitric oxide and free radicals in mediating
N-methyl-D-aspartate (NMDA)-induced increases in adenosine
levels. Rats received unilateral intrastriatal injections and were
sacrificed 15 min postinjection by high-energy focused microwave
irradiation (10 kW, 1.25 s). Adenosine levels were measured by
high-performance liquid chromatography in ipsilateral and contralateral
striata. NMDA and kainic acid dose-dependently increased levels of
adenosine whereas (±)-
-amino-3-hydroxy-5-methyl-4-isoxazol proprionic acid had no effect. The NMDA- and kainic acid-induced increases were blocked by dizocilpine, and the kainic acid response was
decreased by 6-cyano-7-nitroquinoxaline-2,3-dione. The effects of NMDA
and kainic acid on levels of adenosine were not additive. Intrastriatal
L-arginine decreased, and the nitric oxide synthase inhibitor, NG-nitro-L-arginine methyl ester,
increased basal adenosine levels. Coadministration of NMDA with
L-arginine or NG-nitro-L-arginine
methyl ester did not significantly affect NMDA-induced increases in
levels of adenosine. N-Tert-butyl-phenylnitrone, a free
radical scavenger, reversed L-arginine-induced decreases and NMDA-induced increases in levels of adenosine. Together, these results indicate that NMDA-type ionotropic receptors play an important role in regulating in vivo levels of adenosine in rat
striatum and that free radicals, but not nitric oxide, apparently are
involved in NMDA-induced increases in levels of adenosine. Conversely, nitric oxide, but not free radicals, apparently exert tonic control over basal levels of endogenous adenosine.
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