Lardy H, Partridge B, Kneer N, Wei Y
Institute for Enzyme Research, University of Wisconsin, Madison 53705, USA.
Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6617-9. doi: 10.1073/pnas.92.14.6617.
Dehydroepiandrosterone (DHEA), an intermediate in the biosynthesis of testosterone and estrogens, exerts several physiological effects not involving the sex hormones. When fed to rats it induces the thermogenic enzymes mitochondrial sn-glycerol-3-phosphate dehydrogenase and cytosolic malic enzyme in their livers. Animals and humans, and their excised tissues, are known to hydroxylate DHEA at several positions and to interconvert 7 alpha-hydroxy-DHEA, 7 beta-hydroxy-DHEA, 7-oxo-DHEA, and the corresponding derivatives of androst-5-enediol. We report here that these 7-oxygenated derivatives are active inducers of these thermogenic enzymes in rats and that the 7-oxo derivatives are more active than the parent steroids. We postulate that the 7 alpha-hydroxy and 7-oxo derivatives are on a metabolic pathway from DHEA to more active steroid hormones. These 7-oxo steroids have potential as therapeutic agents because of their increased activity and because they are not convertible to either testosterone or estrogens.
脱氢表雄酮(DHEA)是睾酮和雌激素生物合成过程中的一种中间体,具有多种不涉及性激素的生理作用。给大鼠喂食时,它会诱导其肝脏中的产热酶——线粒体甘油-3-磷酸脱氢酶和胞质苹果酸酶。已知动物、人类及其切除的组织会在多个位置使DHEA羟化,并使7α-羟基-DHEA、7β-羟基-DHEA、7-氧代-DHEA以及雄甾-5-烯二醇的相应衍生物相互转化。我们在此报告,这些7-氧化衍生物是大鼠中这些产热酶的活性诱导剂,且7-氧代衍生物比母体类固醇更具活性。我们推测7α-羟基和7-氧代衍生物处于从DHEA到活性更高的类固醇激素的代谢途径上。这些7-氧代类固醇因其活性增加且不能转化为睾酮或雌激素而具有作为治疗剂的潜力。