The P2Y1 receptor closes the N‐type Ca2+ channel in neurones, with both adenosine triphosphates and diphosphates as potent agonists

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Abstract
The rat P2Y1 nucleotide receptor, the P2Y subtype abundant in the brain, was heterologously expressed in rat superior cervical ganglion neurones by micro‐injection of the receptor cRNA or cDNA. ADP inhibited the N‐type Ca2+ current by 64%, with EC50 8.2 nM, an action blocked competitively by the P2Y1 receptor antagonist adenosine 3′, 5′‐bis‐phosphate (Ki 0.7 μM). 2‐Methylthio‐ADP inhibited the Ca2+ current likewise, but with EC50 0.57 nM, giving the highest potency reported therewith for P2Y1. Significantly, ATP and 2‐methylthio‐ATP were also agonists, the latter again at a very high potency (EC50 2.5 nM). We propose that this neuronal receptor, when present in brain at a high density as at synapses, can respond to very low concentrations of ATP and ADP as agonists, and that this would result in inhibition of N‐type Ca2+ currents and hence can reduce transmitter release or increase neuronal excitability.British Journal of Pharmacology (2000) 129, 1063–1066; doi:10.1038/sj.bjp.0703185