Jay D, Cuéllar A, Zamorano R, Muñoz E, Gleason R
Departamento de Bioquímica, Instituto Nacional de Cardiología, Ignacio Chávez, México City, México.
Arch Biochem Biophys. 1991 Nov 1;290(2):463-7. doi: 10.1016/0003-9861(91)90567-3.
The purpose of this study was to use a direct method, that of electron spin resonance spectroscopy, to evaluate the ability of captopril, an angiotensin-converting enzyme inhibitor, to prevent the superoxide-mediated formation of phenyl radicals. Results indicate that, under certain conditions, captopril is a potent inhibitor of the generation of phenyl radicals, produced by the autoxidation of phenylhydrazine. The inhibitory effect of captopril, however, was better understood as a direct interaction of the drug with the metals that catalyze the autoxidation process rather than as a reaction of captopril with the free radicals generated. This last conclusion was supported by the finding that captopril was not able to inhibit the superoxide anion-mediated reduction of nitroblue tetrazolium.