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新生儿期睾酮过量会导致野生型小鼠出现雄性特异性社交和恐惧记忆缺陷。

Excess Neonatal Testosterone Causes Male-Specific Social and Fear Memory Deficits in Wild-Type Mice.

作者信息

Quiñones-Labernik Pravda, Blocklinger Kelsey L, Bruce Matthew R, Hagan Emily, Preuschl Danielle, Tesar Charlotte, Ferri Sarah L

机构信息

Department of Neuroscience and Pharmacology, University of Iowa, Iowa City, Iowa 52242.

Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242.

出版信息

eNeuro. 2025 Aug 1;12(8). doi: 10.1523/ENEURO.0020-25.2025. Print 2025 Aug.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af0/12320760/051e48940371/eneuro-12-ENEURO.0020-25.2025-g001.jpg

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