Pagé N, Warriar N, Govindan M V
Medical Research Council Group in Molecular Endocrinology, Laval University Medical Center, Quebec, Canada.
Am J Physiol. 1994 Oct;267(4 Pt 1):L464-74. doi: 10.1152/ajplung.1994.267.4.L464.
Selectivity to aldosterone (Aldo) in mineralocorticoid target tissues has been suggested to be due to the activity of 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD). This enzyme inactivates the endogenous glucocorticoid cortisol, thus permitting the unhindered access of Aldo to the mineralocorticoid receptor. The 11 beta-HSD activity was measured by the conversion of cortisol to cortisone and vice versa. Concomitant treatment of the cells with either cortisone or cortisol in the presence of the glycyrrhetinic acid derivative carbenoxolone (CBX) blocked both activities of 11 beta-HSD. Dexamethasone and Aldo activated the transcription of transiently transfected mouse mammary tumor virus-bacterial chloramphenicol acetyltransferase chimeric gene in LU-19 cells. The transcription activation by cortisol was synergized by concomitant treatment of the transfectants with CBX. Transactivation with Aldo was inhibited by spironolactone. The enzyme 11 beta-HSD in LU-19 cells is similar to the cloned liver isoform and catalyzes both reduction and dehydrogenation.
有人提出,盐皮质激素靶组织对醛固酮(Aldo)的选择性是由于11β-羟基类固醇脱氢酶(11β-HSD)的活性所致。该酶可使内源性糖皮质激素皮质醇失活,从而使醛固酮能够不受阻碍地作用于盐皮质激素受体。11β-HSD的活性通过皮质醇向可的松的转化以及反之亦然来测定。在甘草次酸衍生物甘珀酸(CBX)存在的情况下,用可的松或皮质醇同时处理细胞会阻断11β-HSD的两种活性。地塞米松和醛固酮可激活LU-19细胞中瞬时转染的小鼠乳腺肿瘤病毒-细菌氯霉素乙酰转移酶嵌合基因的转录。用CBX同时处理转染细胞可增强皮质醇的转录激活作用。醛固酮的反式激活作用被螺内酯抑制。LU-19细胞中的11β-HSD酶与克隆的肝脏同工型相似,可催化还原和脱氢反应。