Quiñones-Labernik Pravda, Blocklinger Kelsey L, Bruce Matthew R, Hagan Emily, Preuschl Danielle, Tesar Charlotte, Ferri Sarah L
Department of Neuroscience and Pharmacology, University of Iowa, Iowa City, Iowa 52242.
Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242.
eNeuro. 2025 Aug 1;12(8). doi: 10.1523/ENEURO.0020-25.2025. Print 2025 Aug.
Neurodevelopmental disorders disproportionately affect males compared with females. The biological mechanisms of this male susceptibility or female protection have not been identified. There is evidence that fetal/neonatal gonadal hormones, which play a pivotal role in many aspects of development, may contribute. Here, we investigate the effects of excess testosterone (T) during a critical period of sex-specific brain organization on social approach and fear learning behaviors in C57BL/6J wild-type mice. Male, but not female, mice treated with T on the day of birth (Postnatal Day 0; PN0) exhibited decreased social approach as juveniles and decreased contextual fear memory as adults, compared with vehicle (veh)-treated controls. These deficits were not driven by anxiety-like behavior or changes in locomotion or body weight. Mice treated with the same dose of T on PN18, which is outside of the critical period of brain masculinization, did not demonstrate impairments compared with the veh group. These findings indicate that excess T during a critical period of early development, but not shortly after, induces long-term deficits relevant to the male sex bias in neurodevelopmental disorders.
与女性相比,神经发育障碍对男性的影响更为严重。这种男性易感性或女性保护性的生物学机制尚未明确。有证据表明,在发育的许多方面起关键作用的胎儿/新生儿性腺激素可能与此有关。在此,我们研究了在性别特异性脑组织结构的关键时期过量睾酮(T)对C57BL/6J野生型小鼠社交趋近和恐惧学习行为的影响。与接受载体(veh)处理的对照组相比,出生当天(出生后第0天;PN0)接受T处理的雄性小鼠在幼年时社交趋近减少,成年时情境恐惧记忆减少,而雌性小鼠则没有。这些缺陷并非由焦虑样行为或运动或体重变化所驱动。在出生后第18天(PN18)接受相同剂量T处理的小鼠,此时已超出脑男性化的关键时期,与veh组相比未表现出损伤。这些发现表明,在早期发育的关键时期而非之后不久过量的T会导致与神经发育障碍中男性性别偏见相关的长期缺陷。