THE INHIBITION OF THE CONSTITUTIVE BOVINE ENDOTHELIAL NITRIC-OXIDE SYNTHASE BY IMIDAZOLE AND INDAZOLE AGENTS

Citrulline formation by the Ca2+ CaM-dependent nitric oxide synthase o f bovine endothelium is inhibited reversibly by 7-nitroindazole, 1-phe nylimidazole, and imidazole. As measured at 0.67 mu M (6R)-5,6,7,8-tet rahydrobiopterin (BH4), IC50 values of 0.8, 200, and 50 mu M were dete rmined for 7-nitroindazole, 1-phenylimidazole, and imidazole, respecti vely. increasing concentrations of added BH, cofactor increased the IC 50 values for 7-nitroindazole and 1-phenylimidazole but did not alter the IC50 value for imidazole. 7-nitroindazole inhibited citrulline for mation by the endothelial cNOS noncompetitively versus arginine substr ate but competitively versus BH4 with a K-i value of 0.8 mu M. 1-pheny limidazole inhibited citrulline formation by the endothelial cNOS comp etitively versus both arginine substrate and BH4 with a K-i value of 5 0 mu M. Imidazole inhibited citrulline formation competitively versus arginine substrate but noncompetitively versus BH4 with a K-i value of 50 mu M. Neither 7-nitroindazole, 1-phenylimidazole, nor imidazole in hibited the cytochrome c reductase activity of endothelial cNOS at con centrations up to 5000-fold higher than their K-i values for inhibitio n of citrulline formation. By comparison with the previously determine d kinetic properties of the other nitric oxide synthase isoforms, thes e observations establish that 1-phenylimidazole displays marked specif icity for inhibiting the inducible nitric oxide synthase isoform and, since 7-nitroindazole has been reported not to elevate blood pressure (McCall ct al., 1991, Br. J. Pharmacol. 102, 234-238), fails to confir m the expected insensitivity of the constitutive endothelial nitric ox ide synthase to inhibition by 7-nitroindazole. (C) 1994 Academic Press , Inc.