Inhibition of lipid synthesis and glucose-6-phosphate dehydrogenase in rat skin by dehydroepiandrosterone

Journal of Lipid Research

Vincent A. Ziboh¹  S.L. Hsia¹  M.A. Dreize¹ 

[1] Departments of Dermatology and Biochemistry, University of Miami School of Medicine, Miami, Florida, 33136;

关键词: 6-phospho-d-gluconate dehydrogenase;    malic enzyme;    polar lipids;    neutral lipids;    lipogenesis;   

DOI  :  

来源: DOAJ

【 摘 要 】

Lipid synthesis from acetate-1-14C by rat skin was inhibited 44-56% by 2.5 × 10-4m dehydroepiandrosterone (DHA) in vitro with or without addition of glucose in the incubation medium. This inhibition affected all the lipid fractions examined (hydrocarbons, sterols, sterol esters, tri-, di- and monoglycerides, fatty acids, and polar lipids) and could be reversed by NADPH. DHA also inhibited lipid synthesis from glucose-U-14C and the formation of 14CO2 from glucose-1-14C, indicating interference with pentose cycle activity. Experiments with the 105,000 g supernatant fluid of rat skin homogenates demonstrated considerable activities of malic enzyme (ME) (12.6 nmoles of NADPH generated per min per mg of protein), of glucose-6-phosphate dehydrogenase (G6PD), and of 6-phosphogluconate dehydrogenase (6PGD) (17.5 nmoles of NADPH generated per min per mg of protein). G6PD was inhibited 98% by 2.5 × 10-4m dehydroepiandrosterone, while 6PGD and ME were not affected. It can be estimated from these data that the pentose cycle may contribute 41-57% of the NADPH needed for lipid synthesis in rat skin; the remainder of the necessary NADPH is presumably supplied by malic enzyme.

【 授权许可】

Unknown