Neuroscience and Behavior Program, Department of Psychology and Center for Neuroendocrine Studies, University of Massachusetts, Amherst, MA 01003, USA.
J Neuroendocrinol. 2011 Oct;23(10):906-14. doi: 10.1111/j.1365-2826.2011.02196.x.
Recent findings demonstrate that epigenetic modifications are required for the sexual differentiation of the brain. For example, neonatal administration of the histone deacetylase inhibitor, valproic acid, blocks masculinisation of cell number in the principal nucleus of the bed nucleus of the stria terminalis (BNST). In the present study, we examined the effects of valproic acid on neurochemistry and behaviour, focusing on traits that are sexually dimorphic and linked to the BNST. Newborn mice were treated with saline or valproic acid and the effect on vasopressin immunoreactivity and olfactory preference behaviour was examined in adulthood. As expected, males had more vasopressin immunoreactive fibres than females in the lateral septum and medial dorsal thalamus, which are two projection sites of BNST vasopressin neurones. Neonatal valproic acid increased vasopressin fibre density specifically in females in the lateral septum, thereby reducing the sex difference, and increased vasopressin fibres in both sexes in the medial dorsal thalamus. The effects were not specific to BNST vasopressin projections, however, because valproic acid also significantly increased vasopressin immunoreactivity in the anterior hypothalamic area in both sexes. Subtle sex-specific effects of neonatal valproic acid treatment were observed on olfactory behaviour. As predicted, males showed a preference for investigating female-soiled bedding, whereas females showed a preference for male-soiled bedding. Valproic acid did not significantly alter olfactory preference, per se, although it increased the number of visits females made to female-soiled bedding and the overall time females spent investigating soiled versus clean bedding. Taken together, these results suggest that a transient disruption of histone deacetylation at birth does not have generalised effects on sexual differentiation, although it does produce lasting effects on brain neurochemistry and behaviour.
最近的研究结果表明,表观遗传修饰对于大脑的性别分化是必需的。例如,新生期给予组蛋白去乙酰化酶抑制剂丙戊酸,可阻断终纹床核主核(BNST)细胞数量的雄性化。在本研究中,我们研究了丙戊酸对神经化学和行为的影响,重点关注与 BNST 相关的具有性别二态性的特征。新生小鼠用生理盐水或丙戊酸处理,成年后检查其对血管加压素免疫反应和嗅觉偏好行为的影响。正如预期的那样,雄性在外侧隔核和内侧背丘脑中的血管加压素免疫反应纤维比雌性多,外侧隔核和内侧背丘脑是 BNST 血管加压素神经元的两个投射部位。新生丙戊酸特异性增加雌性外侧隔核中的血管加压素纤维密度,从而减少性别差异,并增加两性内侧背丘脑中的血管加压素纤维。然而,这些影响并非 BNST 血管加压素投射所特有,因为丙戊酸也显著增加了两性的下丘脑前区中的血管加压素免疫反应。在嗅觉行为方面观察到新生丙戊酸处理的微妙的性别特异性影响。正如预测的那样,雄性表现出对雌性污染垫料的偏好,而雌性表现出对雄性污染垫料的偏好。丙戊酸本身并没有显著改变嗅觉偏好,尽管它增加了雌性对雌性污染垫料的访问次数,并增加了雌性对污染垫料与干净垫料的总体时间。综上所述,这些结果表明,出生时短暂的组蛋白去乙酰化作用中断不会对性别分化产生普遍影响,尽管它确实对大脑神经化学和行为产生持久影响。