Transformation in vitro of [4-14-C]-dehydroepiandrosterone into 7-oxygenated derivatives by normal human male and female skin tissue.
Transformation in vitro of [4-14-C]-dehydroepiandrosterone into 7-oxygenated derivatives by normal human male and female skin tissue.
复制标题
正常人类男性和女性皮肤组织将[4-14-C]-脱氢表雄酮体外转化为7-氧化衍生物。
DOI:
10.1038/jid.1969.61
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发表时间:
1969
期刊:
影响因子:
--
通讯作者:
M. Julesz
中科院分区:
文献类型:
--
作者:
I. Faredin;A. Fazekas;I. Toth;K. Kókai;M. Julesz
It was previously shown that human skin slices intensively metabolized [4-14C]-dehydroepiandrosterone ([4-'°C]-DHA) in vitro (1—3). From the numerous metabolites androst-4-ene3, 17-dione, androsterone and testosterone were isolated and identified. It was suggested that one of the main pathways of DHA metabolism proceeded towards androsterone and testosterone via androst-4-erie-3,17-dione (3, 4). This metabolic pathway was confirmed by incubations with [4-°°C]-androst-4-ene-3, 17-dione (5). By iricubations of [4-°C]-DHA with skin slices strongly polar metabolites i.e. 7-keto-dehydroepiandrosterone (7-keto-DHA) and 7ahydroxy-dehydroepiandrosterone (7a-OH-DHA) were also formed in considerable yields (2, 3). Since the formation of 7-oxygenated derivatives appears to be another metabolic pathway of DHA in the human skin we studied the synthesis of these steroids by incubating [4..'4C]-DHA with abdominal skin samples taken from normal male and female patients in order to obtain merely qualitative data concerning the significance of this second metabolic