DEFIBROTIDE, A SINGLE-STRANDED POLYDEOXYRIBONUCLEOTIDE ACTING AS AN ADENOSINE RECEPTOR AGONIST

The binding of single-stranded polydeoxyribonucleotides to adenosine Al and A2 receptors was investigated. Defibrotide, a natural substance with established anti-thrombotic and anti-ischaemic effects, displaced [H-3]CHA (N6-cyclohexyl-adenosine) and [H-3]NECA (5'-N-ethylcarboxamido-adenosine) concentration dependently, completely and competitively. K(i) values of 371 +/- 68 and 688 +/- 115 mug/ml (mean +/- S.E.M. of 4-5 replications) were computed for adenosine A1 and A2 sites, respectively. Higher and lower molecular weight polydeoxyribonucleotides displayed comparable affinity, whereas a double-stranded polydeoxyribonucleotide and a polyanion with a negative charge comparable to that of defibrotide were inactive. Defibrotide did not affect the total number of binding sites in radioligand saturation experiments. Defibrotide relaxed the K+-contracted guinea-pig trachealis muscle (IC50 = 4001 mug/ml) about one-third as potently as the CHA-contracted preparation and as potently as the resting preparation. NECA, a mixed adenosine A1/A2 receptor agonist, behaved similarly. The effects were abolished by the adenosine A1/A2 receptor blocker 8-phenyltheophylline, but not by the selective A1 blocker, 1,3-dipropyl-8-(2-amino-4-chlorophenyl)-xanthine. These results demonstrate that defibrotide binds to adenosine receptors and triggers pharmacological responses comparable to those of a known agonist.