Bakker Julie, Baum Michael J
Center for Cellular & Molecular Neurobiology, University of Liège, Belgium.
Front Neuroendocrinol. 2008 Jan;29(1):1-16. doi: 10.1016/j.yfrne.2007.06.001. Epub 2007 Jul 26.
The importance of estrogens in controlling brain and behavioral sexual differentiation in female rodents is an unresolved issue in the field of behavioral neuroendocrinology. Whereas, the current dogma states that the female brain develops independently of estradiol, many studies have hinted at possible roles of estrogen in female sexual differentiation. Accordingly, it has been proposed that alpha-fetoprotein, a fetal plasma protein that binds estrogens with high affinity, has more than a neuroprotective role and specifically delivers estrogens to target brain cells to ensure female differentiation. Here, we review new results obtained in aromatase and alpha-fetoprotein knockout mice showing that estrogens can have both feminizing and defeminizing effects on the developing neural mechanisms that control sexual behavior. We propose that the defeminizing action of estradiol normally occurs prenatally in males and is avoided in fetal females because of the protective actions of alpha-fetoprotein, whereas the feminizing action of estradiol normally occurs postnatally in genetic females.
雌激素在控制雌性啮齿动物大脑和行为性分化方面的重要性,是行为神经内分泌学领域一个尚未解决的问题。尽管目前的教条认为雌性大脑的发育独立于雌二醇,但许多研究已经暗示了雌激素在雌性性分化中可能发挥的作用。因此,有人提出,甲胎蛋白这种能与雌激素高亲和力结合的胎儿血浆蛋白,其作用不止是神经保护,还能特异性地将雌激素输送到目标脑细胞以确保雌性分化。在此,我们回顾了在芳香化酶和甲胎蛋白基因敲除小鼠中获得的新结果,这些结果表明雌激素对控制性行为的发育中的神经机制既能产生雌性化作用,也能产生去雌性化作用。我们提出,雌二醇的去雌性化作用通常在雄性胎儿期发生,而由于甲胎蛋白的保护作用,在雌性胎儿中得以避免,而雌二醇的雌性化作用通常在出生后发生在基因雌性个体中。