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Title: Protection of catechol oestrogen from oxidation during enzymic hydrolysis of biliary conjugates. Author: Maggs JL, Grabowski PS, Park BK. Journal: J Steroid Biochem; 1983 Aug; 19(2):1235-7. PubMed ID: 6310265. Abstract: 2-Hydroxyethynyloestradiol (2-OHEE2), a major biliary metabolite of 17 alpha-ethynyloestradiol in female rats, is conjugated largely with glucuronic acid. Accurate quantitation of [3H]2-OHEE2 deconjugated by enzymic hydrolysis depends upon co-incubation with ascorbate (5-10 mM). In the absence of ascorbate, the proportion of [3H]2-OHEE2 declines by 30 +/- 7% (x +/- SD, n = 4) during a 3 h incubation of bile with arylsulphohydrolase and beta-glucuronidase. Over 16 h, decomposition of the catechol leads to a decrease in ether-extractable 3H labelled components.[Abstract] [Full Text] [Related] [New Search]