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母代高脂肪饮食和早期生活应激对幼年和成年大鼠内侧前额叶皮质的棘密度和树突形态有差异调节作用。

Maternal high-fat diet and early life stress differentially modulate spine density and dendritic morphology in the medial prefrontal cortex of juvenile and adult rats.

机构信息

UMR1286, INRA, Nutrition and Integrative Neurobiology (NutriNeuro), Bordeaux, France.

UMR1286, Univ. Bordeaux, Nutrition et Neurobiologie Intégrée, Bordeaux, France.

出版信息

Brain Struct Funct. 2018 Mar;223(2):883-895. doi: 10.1007/s00429-017-1526-8. Epub 2017 Oct 11.

DOI:10.1007/s00429-017-1526-8
PMID:29022091
Abstract

The medial prefrontal cortex (mPFC) is a key area for the regulation of numerous brain functions including stress response and cognitive processes. This brain area is also particularly affected by adversity during early life. Using an animal model in rats, we recently demonstrated that maternal exposure to a high-fat diet (HFD) prevents maternal separation (MS)-induced gene expression alterations in the developing PFC and attenuates several long-term deleterious behavioral effects of MS. In the present study, we ask whether maternal HFD could protect mPFC neurons of pups exposed to early life stress by examining dendritic morphology and spine density in juvenile [postnatal day (PND) 21] and adult rats submitted to MS. Dams were fed either a control or an HFD throughout gestation and lactation, and pups were submitted to MS from PND2 to PND14. We report that maternal HFD prevents MS-induced spine loss at PND21 and dendritic atrophy at adulthood. Furthermore, we show in adult MS rats that PFC-dependent memory extinction deficits are prevented by maternal HFD. Finally, perinatal HFD exposure reverses gut leakiness following stress in pups and seems to exert an anti-stress effect in dams. Overall, our work demonstrates that maternal HFD affects the developing brain and suggests that nutrition, possibly through gut-brain interactions, could modulate mPFC sensitivity to early stress.

摘要

内侧前额叶皮层(mPFC)是调节多种大脑功能的关键区域,包括应激反应和认知过程。这个大脑区域也特别容易受到早期生活逆境的影响。我们最近使用大鼠动物模型证明,母体暴露于高脂肪饮食(HFD)可防止母体分离(MS)引起的发育中的 PFC 基因表达改变,并减轻 MS 的几种长期有害的行为影响。在本研究中,我们通过检查幼年[产后第 21 天(PND21)和成年大鼠]和幼鼠暴露于早期生活应激后 MS 中小鼠 mPFC 神经元的树突形态和棘密度,来探讨母体 HFD 是否可以保护 mPFC 神经元。在整个妊娠和哺乳期,母鼠均喂食对照或 HFD,从 PND2 到 PND14 对幼仔进行 MS。我们报告称,母体 HFD 可防止 MS 引起的 PND21 时的棘突丢失和成年时的树突萎缩。此外,我们在成年 MS 大鼠中表明,母体 HFD 可防止 PFC 依赖性记忆消除缺陷。最后,围产期 HFD 暴露可减轻应激后幼仔的肠道渗漏,并似乎对母体产生抗应激作用。总体而言,我们的工作表明母体 HFD 会影响发育中的大脑,并表明营养可能通过肠道-大脑相互作用来调节 mPFC 对早期应激的敏感性。

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