Why the study?
Does zofenopril improve vascular function and reduce cardiac impairment compared with non-sulphydryl-containing ACE inhibitors?
Does zofenopril improve vascular function and reduce cardiac impairment compared with non-sulphydryl-containing ACE inhibitors?
The sulphydryl ACE inhibitor zofenopril exhibits unique antioxidant and tissue-protective properties that may offer clinical advantages over non-sulphydryl ACE inhibitors in cardiovascular disease management.
Zofenopril's pleiotropic effects may inform ACE inhibitor selection; leaves open clinical superiority over non-sulfhydryl agents pending randomized data.
Zofenopril, a new potent sulphydryl angiotensin-converting enzyme (ACE) inhibitor, is characterized by high lipophilicity, selective cardiac ACE inhibition, and antioxidant and tissue protective activities. In vitro and in vivo experiments suggest that zofenopril exerts antioxidant properties at clinically achievable tissue concentrations. In endothelial cells, zofenopril enhances nitric oxide production, attenuates atherosclerotic lesion development and inhibits adhesion molecule expression by reducing reactive oxygen species. These peculiar characteristics are reflected in the drug's cardioprotective activity, which has been shown to be greater than that of non-sulphydryl ACE inhibitors. Cardiac hypertrophy was also reduced by chronic zofenopril administration, independently of its blood pressure-reducing effect. ACE inhibitors with a sulphydryl group could have an advantage in improving vascular function and reducing cardiac impairment compared with non-sulphydryl-containing ACE inhibitors. This could explain zofenopril's remarkable clinical efficacy post-infarction, and potentially beneficial use in prevention and therapy of cardiovascular diseases, such as atherosclerosis, thrombosis and heart failure.
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Evangelista et al. (2005) studied this question.
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