Turner R T, Wakley G K, Hannon K S
Department of Orthopedics, Mayo Clinic, Rochester, Minnesota 55902.
J Orthop Res. 1990 Jul;8(4):612-7. doi: 10.1002/jor.1100080418.
The physiological role of gonadal androgens in regulating bone metabolism is not established. To determine if androgens antagonize the changes in cortical bone after gonadectomy, we treated orchiectomized (ORX) rats with testosterone (T) and 5 alpha-dihydrotestosterone (DHT), and ovariectomized (OVX) rats with the afore-mentioned androgens, as well as the synthetic androgen fluoxymesterone (Fl) and the nonsteroidal estrogen diethylstilbestrol (DES). OVX resulted in a rapid, sustained increase in periosteal bone formation at the tibial diaphysis, whereas ORX resulted in decreased bone formation. Androgen treatment stimulated bone formation in ORX rats and suppressed bone formation in OVX rats. A large dose of DES suppressed bone formation in OVX rats to values below the intact controls. The results of these studies demonstrate that androgens counteract the changes in cortical bone formation after gonadectomy in females as well as males, and thereby reestablish the sex difference observed in intact rats.
性腺雄激素在调节骨代谢中的生理作用尚未明确。为了确定雄激素是否能拮抗去势后皮质骨的变化,我们用睾酮(T)和5α-双氢睾酮(DHT)处理去势雄鼠(ORX),用上述雄激素以及合成雄激素氟甲睾酮(Fl)和非甾体雌激素己烯雌酚(DES)处理去势雌鼠(OVX)。OVX导致胫骨骨干骨膜骨形成迅速、持续增加,而ORX导致骨形成减少。雄激素治疗刺激ORX大鼠的骨形成并抑制OVX大鼠的骨形成。大剂量DES将OVX大鼠的骨形成抑制到低于完整对照的值。这些研究结果表明,雄激素可抵消雌性和雄性去势后皮质骨形成的变化,从而重新建立在完整大鼠中观察到的性别差异。