Dehydroepiandrosterone sulphate in rat brain: incorporation from blood and metabolism in vivo.

Abstract

AbstractThe incorporation of [7‐3H]dehydroepiandrosterone[35S]sulphate into brain tissue elements from the circulatory system and its metabolic fate in the brain were studied in developing rats. Approximately 0.037 % of [3H] and 0.023% of [35S] were incorporated into the brain within 15 min after the intracardiac injection of the labelled steroid. More than one‐half of the incorporated [3H] was recovered as free steroid, whereas the rest was recovered as sulphate. The 3H/35S ratio in the sulphate fraction suggested that the sulphate entered the brain with the sulphate linkage intact. Upon intracerebral injection of the double‐labelled steroid, approximately 6 per cent of the radioactivity was recovered in the brain at 30 min after the injection and 1 per cent was recovered at 1 h after the injection. Of the remaining radioactivity recovered from the brain, 5 per cent was found in the free steroid fraction, probably formed by hydrolysis of the sulphate; 90 per cent was in the sulphate ester fraction; and the rest was in the fraction of more polar compounds. To identify the metabolites, [4‐14C]dehydroepiandrosterone sulphate was injected into the rat brain. Significant amounts of radioactivity were found in androstenediol sulphate, which was isolated from the brain. This compound was apparently derived from dehydroepiandrosterone sulphate by reduction of the 17‐keto group to a 17β‐hydroxyl group without prior hydrolysis. There was suggestive evidence that free androstenediol was also formed in the brain in this experiment.