Program in Neuroscience (D.M.C., J.A.M.) and Department of Pharmacology (D.M.C., M.M.H., J.A.M.), University of Maryland School of Medicine, Baltimore, Maryland 21201; and Department of Psychology (M.M.H.), University of Nicosia, 1700 Nicosia, Cyprus.
Endocrinology. 2014 Jan;155(1):204-14. doi: 10.1210/en.2013-1624. Epub 2013 Dec 20.
The paucity of clinical and preclinical studies investigating sex differences in sleep has resulted in mixed findings as to the exact nature of these differences. Although gonadal steroids are known to modulate sleep in females, less is known about males. Moreover, little evidence exists concerning the origin of these sex differences in sleep behavior. Thus, the goal of this study was to directly compare the sensitivity of sleep behavior in male and female Sprague Dawley rats to changes in the gonadal steroid milieu and to test whether the sex differences in sleep are the result of brain sexual differentiation or differences in circulating gonadal steroids. Here we report the magnitude of change in sleep behavior induced by either estradiol (E2) or testosterone (T) was greater in females compared with males, suggesting that sleep behavior in females is more sensitive to the suppressive effects of gonadal steroids. Furthermore, we demonstrated that the organizational effects of early gonadal steroid exposure result in male-like responsivity to gonadal steroids and directly alter the activity of the ventrolateral preoptic area (VLPO), an established sleep-promoting nucleus, in adult masculinized females. Moreover, the nonaromatizable androgen dihydrotestosterone did not suppress sleep in either males or females, suggesting that the T-mediated effect in females was due to the aromatization of T into E2. Together our data suggest that, like sex behavior, sex differences in sleep follow the classical organizational/activational effects of gonadal steroids.
关于睡眠中性别差异的临床和临床前研究很少,因此对于这些差异的确切性质存在混合的结果。尽管已知性腺类固醇会调节女性的睡眠,但对男性的了解较少。此外,关于这些睡眠行为性别差异的起源几乎没有证据。因此,本研究的目的是直接比较雄性和雌性 Sprague Dawley 大鼠的睡眠行为对性腺类固醇环境变化的敏感性,并测试睡眠中的性别差异是否是大脑性分化或循环性腺类固醇差异的结果。在这里,我们报告了雌激素(E2)或睾酮(T)引起的睡眠行为变化的幅度在雌性中比雄性更大,这表明雌性的睡眠行为对性腺类固醇的抑制作用更为敏感。此外,我们证明了早期性腺类固醇暴露的组织效应导致雄性对性腺类固醇的反应类似于雄性,并直接改变了成年雄性化雌性中已建立的促进睡眠的腹外侧视前区(VLPO)的活性。此外,非芳香化雄激素二氢睾酮在雄性或雌性中均不能抑制睡眠,这表明 T 在雌性中的介导作用是由于 T 转化为 E2。我们的数据表明,与性行为一样,睡眠中的性别差异遵循性腺类固醇的经典组织/激活作用。