Brönnegård M, Werner S, Gustafsson J A
J Clin Invest. 1986 Nov;78(5):1270-8. doi: 10.1172/JCI112711.
We have studied a woman with an apparent receptor-mediated resistance to cortisol on the basis of elevated 24-h mean plasma cortisol levels and increased urinary free cortisol. Plasma ACTH concentrations were normal but she was resistant to adrenal suppression by dexamethasone. No stigmata of Cushing's syndrome were seen. To study the proposed end-organ resistance to cortisol, we examined the glucocorticoid receptor (GR) in lymphocytes and in fibroblasts from this patient and from her son. Several molecular properties of the GR of lymphocytes from the patient were indistinguishable from that of normal control subjects. In thermolability assays, however, the patient's GR as well as her son's GR showed a striking heat sensitivity at 40 degrees and 45 degrees C when compared with GR from normal persons. In addition, data from the thermolability assays correlated well with the lack at 45 degrees C of dexamethasone-induced decrease in in vitro [3H]thymidine incorporation into lymphocytes derived from both patients.
我们研究了一名女性,基于24小时平均血浆皮质醇水平升高和尿游离皮质醇增加,她表现出明显的受体介导的皮质醇抵抗。血浆促肾上腺皮质激素(ACTH)浓度正常,但她对地塞米松的肾上腺抑制有抵抗。未发现库欣综合征的体征。为了研究提出的对皮质醇的终末器官抵抗,我们检测了该患者及其儿子淋巴细胞和成纤维细胞中的糖皮质激素受体(GR)。患者淋巴细胞GR的几个分子特性与正常对照受试者的无法区分。然而,在热稳定性测定中,与正常人的GR相比,患者及其儿子的GR在40℃和45℃时表现出显著的热敏感性。此外,热稳定性测定的数据与45℃时地塞米松诱导的来自两名患者的淋巴细胞体外[3H]胸苷掺入减少的缺乏密切相关。