Lindzey J, Crews D
Department of Zoology, University of Texas, Austin 78712.
J Endocrinol. 1988 Nov;119(2):265-73. doi: 10.1677/joe.0.1190265.
In many male vertebrates, androgens stimulate, while progesterone inhibits, sexual behaviour. Testicular androgens also control sexual behaviour in males of the lizard Cnemidophorus inornatus. However, administration of progesterone will reinstate sexual behaviour in castrated animals. Increased doses of progesterone did not result in increased numbers of responders; at all doses tested approximately 36% (n = 45) of animals treated with progesterone responded as reliable courters. A high percentage (60-68%) of progesterone-sensitive individuals maintained their sensitivity over a period of months. A synthetic progestin 17,21-dimethyl-19-nor-4,9-pregnadiene-3,20-dione with low rates of metabolism and conversion, also stimulated sexual behaviour in castrated C. inornatus. Finally, the synthetic antiprogestin 11 beta-4-dimethylaminophenyl-17 beta-hydroxy-17 alpha-1-propinyl- 4,9-oestradiene-3-one inhibited the stimulatory effects of progesterone on sexual behaviour but failed to inhibit the stimulatory effects of androgens. These findings indicate an unusual departure from the characteristic pattern of steroid sensitivities of neural centres controlling sexual behaviour.
在许多雄性脊椎动物中,雄激素刺激性行为,而孕酮抑制性行为。睾丸雄激素也控制无饰角蜥雄性的性行为。然而,给去势动物注射孕酮会恢复其性行为。增加孕酮剂量并不会导致有反应的动物数量增加;在所有测试剂量下,用孕酮处理的动物中约36%(n = 45)表现为可靠的求偶者。高比例(60 - 68%)的对孕酮敏感的个体在数月内保持其敏感性。一种代谢和转化率低的合成孕激素17,21 - 二甲基 - 19 - 去甲 - 4,9 - 孕二烯 - 3,20 - 二酮也刺激去势的无饰角蜥的性行为。最后,合成抗孕激素11β - 4 - 二甲基氨基苯基 - 17β - 羟基 - 17α - 1 - 丙炔基 - 4,9 - 雌二烯 - 3 - 酮抑制了孕酮对性行为的刺激作用,但未能抑制雄激素的刺激作用。这些发现表明,在控制性行为的神经中枢的类固醇敏感性特征模式方面存在不寻常的差异。