Cortisol metabolism and its inhibition by glycyrrhetinic acid in the isolated perfused human placental lobule

被引:19
作者
Dodds, HM
Taylor, PJ
Johnson, LP
Mortimer, RH
Pond, SM
Cannell, GR
机构
[1] PRINCESS ALEXANDRA HOSP, DEPT CLIN PHARMACOL, BRISBANE, QLD 4102, AUSTRALIA
[2] ROYAL BRISBANE HOSP, DEPT PATHOL, BRISBANE, QLD 4029, AUSTRALIA
[3] ROYAL BRISBANE HOSP, CONJOINT ENDOCRINE LAB, BRISBANE, QLD 4029, AUSTRALIA
[4] UNIV QUEENSLAND, ROYAL BRISBANE HOSP, DEPT OBSTET & GYNAECOL, BRISBANE, QLD, AUSTRALIA
关键词
D O I
10.1016/S0960-0760(97)00039-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously reported the placental metabolism of prednisolone to prednisone, 20 alpha- and beta-dihydroprednisone and 20 beta-dihydroprednisolone. In this study, the disposition of cortisol was investigated in vitro in the dual perfused, isolated human placental lobule after the addition of cortisol (1.2 mu mol, n = 3 and 12 mu mol, n = 4) to the maternal compartment. Analysis of 5 h maternal and fetal perfusate samples by high performance liquid chromatography-electrospray-tandem mass spectrometry (HPLC-ESI-MS/MS) revealed that cortisol was mainly metabolized to cortisone, but a significant production of 20 alpha-dihydrocortisone, 20 beta-dihydrocortisone, 20 alpha-dihydrocortisol and 20 beta-dihydrocortisol was also detected. Saturability of metabolism but not transfer was demonstrated. Metabolism was eliminated by co-perfusion with the potent 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD) enzyme inhibitor 18 beta-glycyrrhetinic acid (GA). The disposition of GA was analysed using HPLC-atmospheric pressure chemical ionisation-MS/MS (HPLC-APCI-MS/MS). GA was found to transfer from the maternal to the fetal circulations without detectable metabolism during 6 h of perfusion. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:337 / 343
页数:7
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