PT - JOURNAL ARTICLE AU - Luiz Belardinelli AU - John C. Shryock AU - Stephen Snowdy AU - Yi Zhang AU - Angela Monopoli AU - Gianluca Lozza AU - Ennio Ongini AU - Ray A. Olsson AU - Donn M. Dennis TI - The A<sub>2A</sub> Adenosine Receptor Mediates Coronary Vasodilation DP - 1998 Mar 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 1066--1073 VI - 284 IP - 3 4099 - http://jpet.aspetjournals.org/content/284/3/1066.short 4100 - http://jpet.aspetjournals.org/content/284/3/1066.full SO - J Pharmacol Exp Ther1998 Mar 01; 284 AB - The coronary vasodilation caused by adenosine is due to activation of A2 adenosine receptors (A2AdoRs), but the subtype or subtypes of A2AdoR (A2A and/or A2B) that mediate this action are uncertain. The purpose of this study was to test the hypothesis that A2AAdoRs mediate coronary vasodilation caused by exogenous or endogenous adenosine in the guinea pig isolated perfused heart. The newly described A2AAdoR antagonist SCH58261 was used to selectively block A2AAdoRs. Attenuations by SCH58261 of increases in coronary conductance (A2 response) and of atrioventricular nodal conduction time (A1 response) caused by exogenous and endogenous adenosine and by agonists with relative selectivity for A2A and A1AdoRs were measured. The CGS21680-induced increase of coronary conductance was antagonized by SCH58261 in a concentration-dependent and competitive manner with aKB value of 5.01 nm. Also reversed by SCH58261 (60 nmol/L) were the increases in coronary conductance caused by the relatively selective A1AdoR agonists CCPA (70 nM), and (R)-(−)Nb-(2-phenyl-isopropyl)adenosine (60 nM) but not those caused by sodium nitroprusside (1.2 μM) and diltiazem (0.4 μM). SCH58261 (≤100 nM) did not attenuate the A1AdoR-mediated prolongations of S-H interval caused by either adenosine or CCPA. SCH58261 attenuated the coronary vasodilation caused by 50 nM adenosine with an IC50 value of 6.8 ± 0.6 nM. The coronary vasodilations caused by the nucleoside uptake inhibitor draflazine and the adenosine kinase inhibitor iodotubercidin were completely reversed by 60 nM SCH58261 or adenosine deaminase (7 U/ml). Thus, the A2AAdoR plays a major role as mediator of coronary vasodilation caused by exogenous and endogenous adenosine and by AdoR agonists. The American Society for Pharmacology and Experimental Therapeutics