Department of Psychiatry and Behavioral Neurobiology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA; Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
Neurobiol Aging. 2023 Oct;130:141-153. doi: 10.1016/j.neurobiolaging.2023.05.015. Epub 2023 Jun 26.
Socioemotional health is positively correlated with improved cognitive and physical aging. Despite known sex differences in socioemotional behaviors and the trajectory of aging, the interactive effects between sex and aging on socioemotional outcomes are poorly understood. We performed the most comprehensive assessment of sex differences in socioemotional behaviors in C57Bl/6J mice across aging to date. Compared to males, females exhibited decreased anxiety-like behavior and social preference but increased social recognition. With age, anxiety-like behavior, cued threat memory generalization, and social preference increased in both sexes. To investigate potential neural mechanisms underlying these behavioral changes, we analyzed transcriptional neuropathology markers in the ventral hippocampus and found age-related changes in genes related to activated microglia, angiogenesis, and cytokines. Sex differences emerged in the timing, direction, and magnitude of these changes, independent of reproductive senescence in aged females. Interestingly, female-specific upregulation of autophagy-related genes correlated with age-related behavioral changes selectively in females. These novel findings reveal critical sex differences in trajectories of ventral hippocampal aging that may contribute to sex- and age-related differences in socioemotional outcomes.
社会情感健康与认知和身体衰老的改善呈正相关。尽管社会情感行为和衰老轨迹存在已知的性别差异,但性别和衰老对社会情感结果的相互作用仍知之甚少。我们对 C57Bl/6J 小鼠的社会情感行为进行了迄今为止最全面的性别差异评估。与雄性相比,雌性表现出较低的焦虑样行为和社交偏好,但表现出较高的社交识别能力。随着年龄的增长,两性的焦虑样行为、线索威胁记忆泛化和社交偏好都增加了。为了探究这些行为变化的潜在神经机制,我们分析了腹侧海马体中的转录神经病理学标志物,发现与激活小胶质细胞、血管生成和细胞因子相关的基因随年龄变化。这些变化在时间、方向和幅度上存在性别差异,与老年雌性的生殖衰老无关。有趣的是,自噬相关基因的雌性特异性上调与雌性特有的年龄相关行为变化相关。这些新发现揭示了腹侧海马体衰老轨迹中的关键性别差异,这些差异可能导致社会情感结果的性别和年龄差异。