Role for prostaglandins in the regulation of type 1 11β-hydroxysteroid dehydrogenase in human granulosa-lutein cells

被引:13
|
作者
Jonas, Kim C.
Chandras, Christina
Abayasekara, D. Robert E.
Michael, Anthony E.
机构
[1] Univ London Royal Vet Coll, Dept Vet Basic Sci, London NW1 0TU, England
[2] UCL, Royal Free & Univ Coll Med Sch, Dept Biochem & Mol Biol, London WC1E 6BT, England
[3] Univ London St Georges Hosp, Div Clin Dev Sci, Acad Sect Obstet & Gynaecol, Ctr Dev & Endocrine Signalling, London SW17 0RE, England
关键词
D O I
10.1210/en.2006-0723
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
11 beta-Hydroxysteroid dehydrogenase (11 beta HSD) enzymes regulate glucocorticoid availability in target tissues. 11 beta HSD1 is the predominant isoenzyme expressed and active in human granulosa-lutein (hGL) cells. This study investigated the effects of pharmacological inhibitors of prostaglandin ( PG) synthesis on 11 beta HSD1 activities and expression in hGL cells. The consequences for 11 beta HSD1 of increasing exposure of hGL cells to PGs, either by treatment with exogenous PGs or by challenging cells with IL-1 beta, were also assessed. Suppression of basal PG synthesis using four different inhibitors of PG H synthase enzymes [ indomethacin, niflumic acid, meclofenamic acid (MA) and N-(2-cyclohexyloxy-4-nitorophenyl) methane sulfonamide (NS-398)] each resulted in significant decreases in both cortisol oxidation and cortisone reduction.
引用
收藏
页码:5865 / 5872
页数:8
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