Lax E R, Peetz A, Schriefers H
Horm Metab Res. 1986 Dec;18(12):814-7. doi: 10.1055/s-2007-1012446.
The concentrations of hepatic oestrogen receptors and atypical sex hormone-binding protein are regulated by sex hormones in different manners. Ovariectomy of female rats leads to a significant increase in the concentration of hepatic oestrogen receptors, which can be reversed following administration of either androgens or oestrogens. No differences are observed between total binding site and unoccupied receptor concentrations. Intact male rats contain significantly lower total binding site concentrations and these are not affected by either testectomy or subsequent androgen administration. However, treatment of male castrates with oestradiol leads to the induction of typical female levels. It is not possible to determine the concentrations of unoccupied receptors in intact or gonadectomized males, or rats of either sex treated with androgens, due to masking by the moderate affinity, high capacity oestradiol binder (hepatic atypical sex hormone-binding protein, HASP). Oestradiol binding to this protein is not affected by testectomy nor subsequent androgen administration, but is reduced pressed following treatment with oestradiol. It is also induced in ovariectomized rats by androgens. Oestradiol binding to this protein can be prevented by inclusion of sodium thiocyanate in the assay buffer, thereby permitting unhindered measurement of the oestrogen receptor concentrations.
肝脏雌激素受体和非典型性激素结合蛋白的浓度受性激素的调控方式不同。雌性大鼠卵巢切除会导致肝脏雌激素受体浓度显著增加,给予雄激素或雌激素后可使其逆转。总结合位点浓度与未占据受体浓度之间未观察到差异。完整雄性大鼠的总结合位点浓度显著较低,睾丸切除或随后给予雄激素均不影响这些浓度。然而,用雌二醇治疗去势雄性大鼠会导致诱导出典型的雌性水平。由于中等亲和力、高容量的雌二醇结合剂(肝脏非典型性激素结合蛋白,HASP)的掩盖作用,无法确定完整或去势雄性大鼠、或用雄激素处理的任何性别的大鼠中未占据受体的浓度。雌二醇与该蛋白的结合不受睾丸切除或随后给予雄激素的影响,但在用雌二醇处理后会减少。雄激素也可在卵巢切除的大鼠中诱导其产生。在测定缓冲液中加入硫氰酸钠可阻止雌二醇与该蛋白的结合,从而能够不受阻碍地测量雌激素受体浓度。