FEBS Letters · 1995 · 92 citations · 24 references
Life SciencesPharmacologyBiochemical PharmacologyEnzymologyRedox BiochemistryAntioxidant DefenseGlutathione MetabolismReactive Oxygen SpeciesAntioxidant MetabolismAntioxidant PropertiesCaptopril TherapyGlutathione Peroxidase ActivityGlutathione S-transferase ActivityGlutathione SystemManganese Superoxide DismutaseOxidative Stress In Liver Injury
We have characterized the effect of angiotensin converting enzyme (ACE) inhibitors on the activity of CuZn-superoxide dismutase (CuZn-SOD), Mn-superoxide dismutase (Mn-SOD), catalase, and selenium-dependent glutathione peroxidase (Se-GPx). CF1 mice (4-month-old females) were administered water containing enalapril (20 mg/l) or captopril (50 mg/l), during 4 to 11 weeks. After 11 weeks, enalapril treatment caused an increase in the activity of CuZn-SOD, Mn-SOD and Se-GPx, from 19 +/- 4 to 46 +/- 7, 2.1 +/- 0.2 to 3.8 +/- 0.2 units/mg protein and 27 +/- 3 to 54 +/- 3 milliunits/mg protein, respectively. After 11 weeks, captopril treatment increased the activities (P < 0.05) of CuZn-SOD, MnSOD and Se-GPx to 35 +/- 4, 2.9 +/- 0.2 units/mg protein, and 38 +/- 2 milliunits/mg protein, respectively. Catalase activity was not affected by the treatments. These results suggest that ACE inhibitors may protect cell components from oxidative damage by increasing the enzymatic antioxidant defenses.
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Hydroperoxide metabolism in mammalian organs.
B Chance, Helmut Sies, A Boveris · Physiological Reviews · 1979 · 5.8K citations