Different roles of adenosine A 1, A 2A and A 3 receptors in controlling kainate-induced toxicity in cortical cultured neurons

Abstract

Adenosine is a neuromodulator that can control brain damage through activation of A 1, A 2A and A 3 receptors, which are located in both neurons and other brain cells. We took advantage of cultured neurons to investigate the role of neuronal adenosine receptors in the control of neurotoxicity caused by kainate and cyclothiazide. Both A 1, A 2A and A 3 receptors were immunocytochemically identified in cortical neurons. Activation of A 1 receptors with 100 nM CPA did not modify the extent of neuronal death whereas the A 1 receptor antagonist, DPCPX (50 nM), attenuated neurotoxicity by 28 ± 5%, and effect similar to that resulting from the removal of endogenous adenosine with 2 U/ml of adenosine deaminase (27 ± 3% attenuation of neurotoxicity). In the presence of adenosine deaminase, DPCPX had no further effect and CPA now exacerbated neurotoxicity by 42 ± 4%. Activation of A 2A receptor with 30 nM CGS21680 attenuated neurotoxicity by 40 ± 8%, an effect prevented by the A 2A receptor antagonists, SCH58261 (50 nM) or ZM241385 (50 nM), which by themselves were devoid of effect. Finally, neither A 3 receptor activation with Cl-IB-MECA (100–500 nM) nor blockade with MRS1191 (5 μM) modified neurotoxicity. These results show that A 1 receptor activation enhances and A 2A receptor activation attenuates neurotoxicity in cultured cortical neurons, indicating that these two neuronal adenosine receptors directly control neurodegeneration. Interestingly, the control by adenosine of neurotoxicity in cultured neurons is similar to that observed in vivo in newborn animals and is the opposite of what is observed in adult brain preparations where A 1 receptor activation and A 2A receptor blockade are neuroprotective.