Oxidation of 3‐oxygenated Δ⁴‐ and Δ⁵‐C₂₇ steroids by soybean lipoxygenase and rat liver microsomessteroids by soybean lipoxygenase and rat liver microsomes

Abstract

The formation of dioxygenated metabolites of cholesterol, epicholesterol (5-cholesten-3 alpha-ol) 4-cholesten-3 beta-ol, 4-cholesten-3 alpha-one and 4-stigmasten-3-one was studied after incubations with soybean lipoxygenase and linoleic acid. From cholesterol and epicholesterol were formed the 7 alpha-hydroxy, 7 beta-hydroxy-, 7 beta-hydroperoxy-, 7-oxo and 5,6-epoxy-derivatives as well as 6 beta-hydroxy-4-cholesten-3-one. All delta 4-steroids were hydroxylated in the 6 alpha- and 6 beta-positions. The ratios between the yields of 6 beta- and 6 alpha-hydroxylated metabolites varied between 3:1 and 2:1. Incubations with 4-cholesten-3 alpha-ol and 4-cholesten-3 beta-ol also afforded the 4,5-epoxides of these steroids. The ratios between the yields of the 4 beta, 5 beta- and 4 alpha, 5 alpha-epoxides were ca. 4:1 for 4-cholesten 3 beta-ol and ca. 3:2 for 4-cholesten-3 alpha-ol. With iron-supplemented microsomes from rat liver, the compounds formed were qualitatively and quantitatively the same as with soybean lipoxygenase, whereas with 18,000 X g rat liver supernatant fractions the yields of all products formed--except 7 alpha-hydroxycholesterol and 6 beta-hydroxy-4-cholesten-3-one--were markedly decreased. The results indicate the presence of a rat liver microsomal 6 beta-hydroxylase which can use 4-cholesten-3-one as a substrate and extend previous findings of similarities between soybean lipoxygenase and a nonspecific lipoxygenase in rat liver microsomes.