Roselli C E, Stormshak F
Department of Physiology and Pharmacology, Oregon Health and Sciences University, Portland, OR 97201-3098, USA.
J Neuroendocrinol. 2009 Mar;21(4):359-64. doi: 10.1111/j.1365-2826.2009.01828.x.
In our laboratory, the domestic ram is used as an experimental model to study the early programming of neural mechanisms underlying same-sex partner preference. This interest developed from the observation that approximately 8% of domestic rams are sexually attracted to other rams (male-oriented) in contrast to the majority of rams that are attracted to oestrous ewes (female-oriented). One prominent feature of sexual differentiation in many species is the presence of a sexually dimorphic nucleus (SDN) in the preoptic/anterior hypothalamus that is larger in males than in females. Lesion studies in rats and ferrets implicate the SDN in the expression of sexual preferences. We discovered an ovine SDN (oSDN) in the preoptic/anterior hypothalamus that is smaller in male- than in female-oriented rams and similar in size to the oSDN of ewes. Neurones of the oSDN show abundant aromatase expression that is also reduced in male-oriented compared to female-oriented rams. This observation suggests that sexual partner preferences are neurologically hard-wired and could be influenced by hormones. Aromatase-containing neurones constitute a nascent oSDN as early as day 60 of gestation, which becomes sexually dimorphic by day 135 of gestation when it is two-fold larger in males than in females. Exposure of fetal female lambs to exogenous testosterone from days 30-90 of gestation resulted in a masculinised oSDN. These data demonstrate that the oSDN develops prenatally and may influence adult sexual preferences. Surprisingly, inhibition of aromatase activity in the brain of ram foetuses during the critical period did not interfere with defeminisation of adult sexual partner preference or oSDN volume. These results fail to support an essential role for neural aromatase in the sexual differentiation of sheep brain and behaviour. Thus, we propose that oSDN morphology and male-typical partner preferences may instead be programmed through an androgen receptor mechanism not involving aromatisation.
在我们实验室中,家公羊被用作实验模型,以研究同性伴侣偏好背后神经机制的早期编程。这种兴趣源于这样的观察:大约8%的家公羊会被其他公羊(雄性导向)性吸引,而大多数公羊则被发情母羊(雌性导向)吸引。许多物种性分化的一个显著特征是视前区/下丘脑前部存在性二态核(SDN),雄性的该核比雌性的大。对大鼠和雪貂的损伤研究表明SDN与性偏好的表达有关。我们在视前区/下丘脑前部发现了一个绵羊性二态核(oSDN),雄性导向的公羊中的oSDN比雌性导向的公羊中的小,且大小与母羊的oSDN相似。oSDN的神经元显示出丰富的芳香化酶表达,与雌性导向的公羊相比,雄性导向的公羊中该酶表达也减少。这一观察结果表明,性伴侣偏好是由神经硬连接的,并且可能受激素影响。含芳香化酶的神经元早在妊娠60天时就构成了一个新生的oSDN,到妊娠135天时它变得具有性二态性,此时雄性的oSDN比雌性的大两倍。在妊娠30 - 90天期间,将雌性胎羊暴露于外源性睾酮会导致oSDN雄性化。这些数据表明oSDN在产前发育,并且可能影响成年后的性偏好。令人惊讶的是,在关键时期抑制公羊胎儿大脑中的芳香化酶活性,并不干扰成年性伴侣偏好的去雌性化或oSDN体积。这些结果不支持神经芳香化酶在绵羊大脑和行为的性分化中起关键作用。因此,我们提出oSDN的形态和雄性典型的伴侣偏好可能是通过一种不涉及芳香化的雄激素受体机制进行编程的。