Crews D, Godwin J, Hartman V, Grammer M, Prediger E A, Sheppherd R
Department of Zoology, University of Texas, Austin 78712, USA.
J Neurosci. 1996 Nov 15;16(22):7347-52. doi: 10.1523/JNEUROSCI.16-22-07347.1996.
A primary tenet of behavioral neuroendocrinology is that gonadal steroid hormones act on limbic nuclei to activate mating behavior in vertebrates. Traditionally, research has focused on the regulation of male-typical sexual behavior by testicular androgens and female-typical sexual behavior by ovarian estrogen and progesterone. Indeed, progesterone generally is regarded as an antiandrogen, acting centrally to inhibit sexual behavior in males. However, experiments with lizards, and more recently with rats, have challenged this paradigm. For example, exogenous progesterone induces mating behavior in some, but not all, castrated male whiptail lizards. The present study determined that implantation of progesterone into the anterior hypothalamus preoptic area of castrated, progesterone-sensitive males completely restored sexual behavior but failed to elicit sexual activity in castrated, progesterone-insensitive males. Further, androgen receptor -and progesterone receptor-mRNA expression in specific brain regions was significantly different in progesterone-sensitive versus progesterone-insensitive animals. Progesterone-sensitive males showed significantly higher relative abundance of androgen receptor-mRNA in the preoptic area, amygdala, and lateral septum, as compared with progesterone-insensitive animals receiving the same treatment. In contrast, progesterone receptor-mRNA abundance was lower in preoptic area of progesterone-sensitive males than in progesterone-insensitive males. No differences were found in the baseline abundance of androgen receptor-or progesterone receptor-mRNA in these nuclei between control groups of progesterone-sensitive and progesterone-insensitive males who were castrated but not implanted. This suggests that progesterone differentially regulates its own receptor as well as androgen receptor in areas of the brain involved in the control of sexual behavior of males and that the nature of this regulation shows individual variability.
行为神经内分泌学的一个主要原则是,性腺类固醇激素作用于边缘核,以激活脊椎动物的交配行为。传统上,研究主要集中在睾丸雄激素对雄性典型性行为的调节以及卵巢雌激素和孕酮对雌性典型性行为的调节。事实上,孕酮通常被视为一种抗雄激素,在中枢发挥作用以抑制雄性的性行为。然而,对蜥蜴以及最近对大鼠的实验对这一范式提出了挑战。例如,外源性孕酮能诱导一些(但不是所有)去势雄性鞭尾蜥的交配行为。本研究确定,将孕酮植入去势的、对孕酮敏感的雄性动物的下丘脑视前区前部可完全恢复性行为,但对去势的、对孕酮不敏感的雄性动物却未能引发性活动。此外,在对孕酮敏感和不敏感的动物中,特定脑区的雄激素受体和孕酮受体mRNA表达存在显著差异。与接受相同处理的对孕酮不敏感的动物相比,对孕酮敏感的雄性动物在视前区、杏仁核和外侧隔中雄激素受体mRNA的相对丰度显著更高。相反,对孕酮敏感的雄性动物视前区的孕酮受体mRNA丰度低于对孕酮不敏感的雄性动物。在未植入孕酮的去势的对孕酮敏感和不敏感的雄性动物对照组中,这些核团中雄激素受体或孕酮受体mRNA的基线丰度没有差异。这表明孕酮在参与控制雄性性行为的脑区中对其自身受体以及雄激素受体有不同的调节作用,并且这种调节的性质存在个体差异。