Seckl J R, Chapman K E
Molecular Endocrinology Unit, Molecular Medicine Centre, University of Edinburgh, Western General Hospital, UK.
Eur J Biochem. 1997 Oct 15;249(2):361-4. doi: 10.1111/j.1432-1033.1997.t01-1-00361.x.
11Beta-hydroxysteroid dehydrogenases (11beta-HSD) catalyse the interconversion of active glucocorticoids (cortisol, corticosterone) and their inert 11-keto derivatives (cortisone, 11-dehydrocorticosterone). The type-2 isozyme (11beta-HSD-2) is a high-affinity dehydrogenase that catalyses the rapid inactivation of glucocorticoids, thus ensuring selective access of aldosterone to otherwise non-selective mineralocorticoid receptors in the distal nephron. Mutations of the gene encoding 11beta-HSD-2 are responsible for the syndrome of apparent mineralocorticoid excess, in which cortisol illicitly occupies mineralocorticoid receptors, causing hypertension and hypokalaemia. 11Beta-HSD-2 is also highly expressed in the placenta and mid-gestation fetus, where it may protect developing tissues from the often deleterious actions of glucocorticoids upon fetal growth and organ maturation. 11Beta-HSD-1 is probably an 11beta-reductase in vivo. Its function is obscure, but may amplify glucocorticoid action during the diurnal nadir, drawing upon the substantial circulating levels of 11-keto steroids. Both isozymes are regulated during ontogeny and by a series of hormonal and other factors. 11Beta-HSD provide an important control of glucocorticoid action at a cellular level, and may represent new targets for therapeutic intervention.
11β-羟类固醇脱氢酶(11β-HSD)催化活性糖皮质激素(皮质醇、皮质酮)与其无活性的11-酮衍生物(可的松、11-脱氢皮质酮)之间的相互转化。2型同工酶(11β-HSD-2)是一种高亲和力脱氢酶,可催化糖皮质激素的快速失活,从而确保醛固酮选择性地作用于远曲小管中原本无选择性的盐皮质激素受体。编码11β-HSD-2的基因突变是导致表观盐皮质激素增多综合征的原因,在该综合征中,皮质醇非法占据盐皮质激素受体,导致高血压和低钾血症。11β-HSD-2在胎盘和妊娠中期胎儿中也高度表达,在那里它可能保护发育中的组织免受糖皮质激素对胎儿生长和器官成熟的常见有害作用。11β-HSD-1在体内可能是一种11β-还原酶。其功能尚不清楚,但可能在昼夜最低点时放大糖皮质激素的作用,利用循环中大量的11-酮类固醇。两种同工酶在个体发育过程中以及受一系列激素和其他因素的调节。11β-HSD在细胞水平上对糖皮质激素作用提供重要控制,可能代表治疗干预的新靶点。