Feedback facilitation by adenosine A2A receptors of ATP release from mouse hippocampal nerve terminals.

Abstract

The adenosine modulation system is mostly composed by inhibitory A₁ receptors (A₁R) and the less abundant facilitatory A_2A receptors (A_2AR), the latter selectively engaged at high frequency stimulation associated with synaptic plasticity processes in the hippocampus. A_2AR are activated by adenosine originated from extracellular ATP through ecto-5'-nucleotidase or CD73-mediated catabolism. Using hippocampal synaptosomes, we now investigated how adenosine receptors modulate the synaptic release of ATP. The A_2AR agonist CGS21680 (10-100 nM) enhanced the K⁺-evoked release of ATP, whereas both SCH58261 and the CD73 inhibitor α,β-methylene ADP (100 μM) decreased ATP release; all these effects were abolished in forebrain A_2AR knockout mice. The A₁R agonist CPA (10-100 nM) inhibited ATP release, whereas the A₁R antagonist DPCPX (100 nM) was devoid of effects. The presence of SCH58261 potentiated CPA-mediated ATP release and uncovered a facilitatory effect of DPCPX. Overall, these findings indicate that ATP release is predominantly controlled by A_2AR, which are involved in an apparent feedback loop of A_2AR-mediated increased ATP release together with dampening of A₁R-mediated inhibition. This study is a tribute to María Teresa Miras-Portugal.