Caputo C B, Meadows D, Raisz L G
Endocrinology. 1976 Apr;98(4):1065-8. doi: 10.1210/endo-98-4-1065.
The effects of estrogens, androgens, and glucocorticoids on bone resorption were compared in organ culture. At a concentration of 10(-5) M, corticosterone, testosterone, dihydrotestosterone, dehydroepiandosterone, estradiol, ethinyl estradiol and estrone did not inhibit the release of 45Ca from 19-day fetal rat long bone shafts in control or para-thyroid hormone (PTH)-treated cultures after 2 or 5 days. Cortisol inhibited both control and PTH-stimulated resorption at 10(-5) M and 10(-6) M. 17beta-Estradiol was inhibitory at 3 X 10(4) M. However, it was less effective than the estrogenically inactive epimer 17alpha-estradiol, in 8 day control cultures or in cultures containing low concentrations of PTH. At 10(-5) m, neither 17beta-estradiol nor 17alpha-estradiol inhibited resorption stimulated by prostaglandin E2 or by osteoclast activating factor.
在器官培养中比较了雌激素、雄激素和糖皮质激素对骨吸收的影响。在浓度为10⁻⁵M时,皮质酮、睾酮、二氢睾酮、脱氢表雄酮、雌二醇、炔雌醇和雌酮在2天或5天后,对对照或甲状旁腺激素(PTH)处理的培养物中19天胎鼠长骨干中⁴⁵Ca的释放没有抑制作用。皮质醇在10⁻⁵M和10⁻⁶M时抑制对照和PTH刺激的骨吸收。17β-雌二醇在3×10⁻⁴M时具有抑制作用。然而,在8天的对照培养物或含有低浓度PTH的培养物中,它的效果不如雌激素无活性的差向异构体17α-雌二醇。在10⁻⁵M时,17β-雌二醇和17α-雌二醇均不抑制前列腺素E2或破骨细胞激活因子刺激的骨吸收。