Activation of particulate guanylyl cyclase by endothelins in cultured SV-40 transformed cat iris sphincter smooth muscle cells

We investigated the effects of endothelins (ETs) on cGMP production in cult ured SV-40 transformed cat iris sphincter smooth muscle (SV-CISM-2) cells. ET-3 increased cGMP formation in a concentration-dependent manner (EC50 = 9 8nM), which was 2.5 times higher than that of ET-1. The ETB receptor agonis ts sarafotoxin-S6c and IRL 1620 also increased cGMP production, mimicking t he effects of the ETs. The ETB receptor antagonist BQ 788, but not the ETA receptor antagonist BQ610, dose-dependently blocked ET3-stimulated cGMP for mation (IC50=10nM). The phorbol ester, Phorbol 12, 13 - dibutyrate (PDBu), which inhibits particulate guanylyl cyclase in smooth muscle, dose-dependen tly inhibited ET-3-stimulated cGMP accumulation (IC50-66nM). LY83583 and OD Q, inhibitors of soluble guanylyl cyclases, as well as inhibitors of the ni tric oxide cascade and of intracellular Ca2+ elevation had no appreciable e ffect on ET-3-induced cGMP production. ET-3 markedly inhibited carbachol-in duced intracellular Ca2+ mobilization. We conclude that ET-3 increases intr acellular cGMP levels in SV-CISM-2 cells through activation of the ETB rece ptor subtype and subsequent stimulation of the membrane-bound guanylyl cycl ase. Elevation of cGMP by ET and the subsequent inhibition of muscarinic st imulation of intracellular Ca2+ mobilization by the cyclic nucleotide could serve to modulate the contractile effects of Ca2+-mobilizing agonists in t he iris sphincter smooth muscle.