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性别特异性行为和分子反应对母体脂多糖诱导免疫激活的在一个小鼠模型中的影响:对神经发育障碍的影响。

Sex-Specific Behavioral and Molecular Responses to Maternal Lipopolysaccharide-Induced Immune Activation in a Murine Model: Implications for Neurodevelopmental Disorders.

机构信息

The Key Laboratory of Molecular Epigenetics of Ministry of Education, Institute of Genetics and Cytology, School of Life Science, Northeast Normal University, Changchun 130024, China.

Jilin Provincial Key Laboratory of Cognitive Neuroscience and Brain Development, School of Psychology, Northeast Normal University, Changchun 130024, China.

出版信息

Int J Mol Sci. 2024 Sep 13;25(18):9885. doi: 10.3390/ijms25189885.

Abstract

Maternal immune activation (MIA) during pregnancy has been increasingly recognized as a critical factor in the development of neurodevelopmental disorders, with potential sex-specific impacts that are not yet fully understood. In this study, we utilized a murine model to explore the behavioral and molecular consequences of MIA induced by lipopolysaccharide (LPS) administration on embryonic day 12.5. Our findings indicate that male offspring exposed to LPS exhibited significant increases in anxiety-like and depression-like behaviors, while female offspring did not show comparable changes. Molecular analyses revealed alterations in pro-inflammatory cytokine levels and synaptic gene expression in male offspring, suggesting that these molecular disruptions may underlie the observed behavioral differences. These results emphasize the importance of considering sex as a biological variable in studies of neurodevelopmental disorders and highlight the need for further molecular investigations to understand the mechanisms driving these sex-specific outcomes. Our study contributes to the growing evidence that prenatal immune challenges play a pivotal role in the etiology of neurodevelopmental disorders and underscores the potential for sex-specific preventative approaches of MIA.

摘要

母体免疫激活(MIA)在怀孕期间被越来越多地认为是神经发育障碍发展的关键因素,其潜在的性别特异性影响尚不完全清楚。在这项研究中,我们使用了一种鼠类模型来探讨在胚胎第 12.5 天用脂多糖(LPS)处理诱导的 MIA 对后代的行为和分子后果。我们的研究结果表明,雄性后代暴露于 LPS 后表现出明显的焦虑样和抑郁样行为增加,而雌性后代则没有表现出类似的变化。分子分析显示雄性后代中促炎细胞因子水平和突触基因表达的改变,表明这些分子紊乱可能是观察到的行为差异的基础。这些结果强调了在神经发育障碍研究中考虑性别作为生物学变量的重要性,并突出了进一步进行分子研究以了解驱动这些性别特异性结果的机制的必要性。我们的研究为越来越多的证据表明,产前免疫挑战在神经发育障碍的发病机制中起着关键作用,并强调了针对 MIA 的性别特异性预防方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0557/11432365/93110538cb9c/ijms-25-09885-g001.jpg

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