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早期前额叶皮层抑制和早期生活应激会导致持久的行为、转录和生理损伤。

Early-life prefrontal cortex inhibition and early-life stress lead to long-lasting behavioral, transcriptional, and physiological impairments.

机构信息

Emotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, 10962, USA.

Department of Child and Adolescent Psychiatry, New York University Grossman School of Medicine, New York, NY, 10016, USA.

出版信息

Mol Psychiatry. 2024 Aug;29(8):2359-2371. doi: 10.1038/s41380-024-02499-4. Epub 2024 Mar 14.

Abstract

Early-life stress has been linked to multiple neurodevelopmental and neuropsychiatric deficits. Our previous studies have linked maternal presence/absence from the nest in developing rat pups to changes in prefrontal cortex (PFC) activity. Furthermore, we have shown that these changes are modulated by serotonergic signaling. Here we test whether changes in PFC activity during early life affect the developing cortex leading to behavioral alterations in the adult. We show that inhibiting the PFC of mouse pups leads to cognitive deficits in the adult comparable to those seen following maternal separation. Moreover, we show that activating the PFC during maternal separation can prevent these behavioral deficits. To test how maternal separation affects the transcriptional profile of the PFC we performed single-nucleus RNA-sequencing. Maternal separation led to differential gene expression almost exclusively in inhibitory neurons. Among others, we found changes in GABAergic and serotonergic pathways in these interneurons. Interestingly, both maternal separation and early-life PFC inhibition led to changes in physiological responses in prefrontal activity to GABAergic and serotonergic antagonists that were similar to the responses of more immature brains. Prefrontal activation during maternal separation prevented these changes. These data point to a crucial role of PFC activity during early life in behavioral expression in adulthood.

摘要

早期生活压力与多种神经发育和神经精神缺陷有关。我们之前的研究将发育中的幼鼠巢内是否存在母体与前额叶皮层(PFC)活动的变化联系起来。此外,我们还表明,这些变化受 5-羟色胺能信号的调节。在这里,我们测试了生命早期 PFC 活动的变化是否会影响发育中的皮层,从而导致成年后的行为改变。我们发现,抑制幼鼠的 PFC 会导致成年后的认知缺陷,类似于母体分离后观察到的情况。此外,我们还发现,在母体分离期间激活 PFC 可以预防这些行为缺陷。为了测试母体分离如何影响 PFC 的转录谱,我们进行了单细胞 RNA-seq 分析。母体分离导致 PFC 中几乎仅抑制性神经元的基因表达存在差异。其中,我们发现这些中间神经元中的 GABA 能和 5-羟色胺能途径发生了变化。有趣的是,母体分离和生命早期 PFC 抑制都导致了前额叶对 GABA 能和 5-羟色胺能拮抗剂的生理反应发生变化,这些变化与更不成熟的大脑的反应相似。母体分离期间的 PFC 激活可防止这些变化。这些数据表明,生命早期 PFC 活动在成年期的行为表达中起着至关重要的作用。

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