CAFFEINE ALTERS GLUTAMATE-ASPARTATE TRANSPORTER FUNCTION AND EXPRESSION IN RAT RETINA

L-Glutamate and L-aspartate are the main excitatory amino acids (EAAs) in the Central Nervous System (CNS) and their uptake regulation is critical for the maintenance of the excitatory balance. Excitatory amino acid transporters (EAATs) are widely distributed among central neurons and glial cells. GLAST and GLT1 are expressed in glial cells, whereas excitatory amino acid transporter 3/excitatory amino acid carrier 1 (EAAT3/EAAC1) is neuronal. Different signaling pathways regulate glutamate uptake by modifying the activity and expression of EAATs. In the present work we show that immature postnatal day 3 (PN3) rat retinas challenged by L-glutamate release [H-3]-D-Aspartate linked to the reverse transport, with participation of NMDA, but not of non-NMDA receptors. The amount of [H-3]-D-Aspartate released by L-glutamate is reduced during retinal development. Moreover, immature retinae at PN3 and PN7, but not PN14, exposed to a single dose of 200 or 500 mu M caffeine or the selective A2A receptor (A2AR) antagonist 100 nM ZM241385 decreased [H-3]-D-Aspartate uptake. Caffeine also selectively increased total expression of EAAT3 at PN7 and its expression in membrane fractions. However, both EAAT1 and EAAT2 were reduced after caffeine treatment in P2 fraction. Addition of 100 nM DPCPX, an A1 receptor (A1R) antagonist, had no effect on the [H-3]-D-Aspartate uptake. [H-3]-D-Aspartate release was dependent on both extracellular sodium and DL-TBOA, but not calcium, implying a transporter-mediated mechanism. Our results suggest that in the developing rat retina caffeine modulates [H-3]-D-Aspartate uptake by blocking adenosine A2AR. (C) 2016 IBRO. Published by Elsevier Ltd. All rights reserved.