Tesone M, Oliveira-Filho R M, Valle L B, Barañao J L, Foglia V G, Charreau E H
Horm Metab Res. 1982 May;14(5):237-40. doi: 10.1055/s-2007-1018981.
It is shown that the binding of the synthetic androgen [3H] methyltrienolone ([3H] R1881) to the nuclear fraction of prostates of streptozotocin-diabetic rats is 38% reduced in comparison to controls. Although the exogenous replacement therapy of diabetic animals wih insulin was capable of restoring to normality several body and tissue parameters, the androgen binding capacity of prostate nuclei is not recovered. Normal binding values were observed in diabetic animals which have been treated with exogenous testosterone. It is postulated that the decrease in the nuclear androgen receptor content in the prostatic gland of streptozotocin-diabetic rats is due to the lower circulating testosterone levels in these animals.
结果显示,与对照组相比,合成雄激素[3H]甲基三烯olone([3H]R1881)与链脲佐菌素诱导的糖尿病大鼠前列腺细胞核部分的结合减少了38%。尽管用胰岛素对糖尿病动物进行外源性替代疗法能够使多个身体和组织参数恢复正常,但前列腺细胞核的雄激素结合能力并未恢复。在用外源性睾酮治疗的糖尿病动物中观察到了正常的结合值。据推测,链脲佐菌素诱导的糖尿病大鼠前列腺中核雄激素受体含量的降低是由于这些动物循环睾酮水平较低所致。