Abstract
We have examined the inhibition of human hepatic microsomal androstenedione 6β-hydroxylation and both reductive and oxidative 17β-hydroxysteroid dehydrogenase (17β-HSD) activity by complex phenols found in olive oil. Structurally similar compounds were also examined for comparison. Androstenedione 6β-hydroxylase activity was inhibited by oleuropein glycoside, hydroxytyrosol and gallic acid. Oleuropein glycoside, hydroxytyrosol, gallic acid and dihydroxybenzoic acid also inhibited reductive 17β-HSD activity. Oxidative 17β-HSD activity was not inhibited by any of the compounds tested; however gallic acid stimulated activity by ~30%. Androstenedione 6β-hydroxylase activity showed atypical kinetics. For oleuropein glycoside, hydroxytyrosol and gallic acid the apparent K(i) values were determined to be 80, 77 and 70 μmol/L, respectively. Analysis of structural features of inhibitory compounds established that a 3,4-dihydroxyphenyl ethanol structure was required for inhibition of androstenedione 6β-hydroxylase for this group of compounds.
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Stupans, I., Stretch, G., & Hayball, P. (2000). Olive oil phenols inhibit human hepatic microsomal activity. Journal of Nutrition, 130(9), 2367–2370. https://doi.org/10.1093/jn/130.9.2367
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