Schlechte J A, Sherman B M
J Clin Endocrinol Metab. 1982 Jan;54(1):145-9. doi: 10.1210/jcem-54-1-145.
To examine the effect of glucocorticoid deficiency on the glucocorticoid receptor, we examine the binding of [3H] dexamethasone to lymphocytes in normal subjects and patients with adrenal insufficiency before and after glucocorticoid replacement therapy. Using a whole cell competitive binding assay, normal human lymphocytes had 5977 +/- 1487 (mean +/- SD) binding sites/cell and a dissociation constant of 10 +/- 2 nM. Lymphocytes from patients with untreated adrenal insufficiency had fewer binding sites (3364 +/-322) and a 2-fold increase in binding affinity (5.4 +/- 0.9 mM). The administration of conventional replacement doses of cortisone acetate for 6 months caused no change in receptor number, but was associated with a decrease in binding affinity toward normal. After long term glucocorticoid replacement therapy, binding parameters were similar to those in patients before treatment. The physiological implications of the decreased receptor number and increased binding affinity in adrenal insufficiency remain to be elucidated.
为研究糖皮质激素缺乏对糖皮质激素受体的影响,我们检测了正常受试者以及肾上腺功能不全患者在糖皮质激素替代治疗前后淋巴细胞对[3H]地塞米松的结合情况。采用全细胞竞争性结合试验,正常人类淋巴细胞每细胞有5977±1487(均值±标准差)个结合位点,解离常数为10±2 nM。未经治疗的肾上腺功能不全患者的淋巴细胞结合位点较少(3364±322),结合亲和力增加了2倍(5.4±0.9 mM)。给予常规替代剂量的醋酸可的松6个月,受体数量未发生变化,但与结合亲和力降至正常水平有关。长期糖皮质激素替代治疗后,结合参数与治疗前患者的参数相似。肾上腺功能不全时受体数量减少和结合亲和力增加的生理意义仍有待阐明。