Effects of SCA40 on bovine trachealis muscle and on cyclic nucleotide phosphodiesterases

Abstract

While UK-93,928 (1-[[3-(6,9-dihydro-6-oxo-9-propyl-1H-purin-2-yl)-4-ethoxyphenyl] sulfonyl]-4-methylpiperazine; 5 nM-5 μM) was devoid of relaxant activity, benzafentrine, isoprenaline, levcromakalim and SCA40 (6-bromo-8-methylaminoimidazo [1,2-a]pyrazine-2-carbonitrile) each relaxed histamine (460 μM)-precontracted bovine isolated trachealis. Each of these relaxants was antagonised by a K +-rich (80 mM) medium. Except in the case of levcromakalim, nifedipine (1 μM) offset this antagonism. Charybdotoxin (100 nM) antagonised isoprenaline in a nifedipine-sensitive manner but did not antagonise SCA40 or benzafentrine. Iberiotoxin (100 nM) did not antagonise SCA40. Acting on tissue precontracted with carbachol, SCA40 potentiated isoprenaline but did not potentiate sodium nitroprusside. While levcromakalim (1 and 10 μM) induced hyperpolarisation, SCA40 (1 and 10 μM) induced little change in the membrane potential of bovine trachealis. In trachealis preloaded with 86Rb +, levcromakalim (1 and 10 μM) promoted efflux of the radiotracer while SCA40 (1 and 10 μM) had no effect. Tested as an inhibitor of isoenzymes of cyclic nucleotide phosphodiesterase, SCA40 was most potent against the type III, less potent against the type IV and least potent against the type I isoenzyme. It is concluded that neither inhibition of phosphodiesterase type V nor the promotion of BK(Ca) channel opening explains the tracheal smooth muscle relaxant activity of SCA40. This compound relaxes bovine tracheal smooth muscle mainly by inhibiting phosphodiesterase isoenzyme types III and IV.