Premium
Neuronal A 1 receptors mediate increase in extracellular kynurenic acid after local intrastriatal adenosine infusion
Author(s) -
Wu HuiQiu,
Fuxe Kjell,
Schwarcz Robert
Publication year - 2004
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2004.02531.x
Subject(s) - adenosine , kynurenic acid , adenosine a1 receptor , adenosine receptor , chemistry , cgs 21680 , adenosine receptor antagonist , pharmacology , adenosine a3 receptor , agonist , purinergic signalling , adenosine deaminase , adenosinergic , microdialysis , extracellular , medicine , receptor , endocrinology , glutamate receptor , biology , biochemistry
The naturally occurring purine nucleoside adenosine has pronounced anticonvulsant and neuroprotective properties and plays a neuromodulatory role in the CNS. Kynurenic acid (KYNA) is an astrocyte‐derived, endogenous neuroinhibitory compound, which shares several of adenosine's properties. In a first attempt to examine possible interactions between these two biologically active molecules, adenosine was focally applied into the striatum of freely moving rats by reverse microdialysis, and changes in extracellular KYNA were monitored over time. A 2‐h infusion of adenosine increased KYNA levels in a dose‐dependent manner, with 10 m m of adenosine causing a twofold elevation within 1 h. This effect was reversible and was effectively blocked by coinfusion of the specific A 1 adenosine receptor antagonist 8‐cyclopentyltheophylline (100 µ m ). In contrast, coinfusion of adenosine with MSX‐3 (100 µ m ), an A 2A receptor antagonist, did not affect the adenosine‐induced increase in KYNA levels . Local striatal perfusion with the A 1 receptor agonist N 6 ‐cyclopentyladenosine (100 µ m ) mimicked the effect of adenosine, whereas perfusion with the A 2A receptor agonist CGS‐21680 (100 µ m ) was ineffective. Finally, we tested the effect of adenosine (10 m m ) on extracellular KYNA in striata that had been injected with quinolinate (60 nmol/1 µL) 7 days earlier. In this neuron‐depleted tissue, perfusion with adenosine failed to affect extracellular KYNA levels. These data demonstrate that adenosine is capable of raising extracellular KYNA in the rat striatum by interacting with postsynaptic neuronal A 1 receptors. This mechanism may result in a synergism between the neurobiological effects of adenosine and KYNA.