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母体缺铁和产前免疫激活对大鼠后代成年行为的叠加效应。

Additive effects of maternal iron deficiency and prenatal immune activation on adult behaviors in rat offspring.

机构信息

Department of Psychiatry, McGill University, Douglas Mental Health University Institute, 6875 La Salle Blvd, Verdun H4H 1R3, Quebec, Canada.

Department of Psychiatry, McGill University, Douglas Mental Health University Institute, 6875 La Salle Blvd, Verdun H4H 1R3, Quebec, Canada.

出版信息

Brain Behav Immun. 2014 Aug;40:27-37. doi: 10.1016/j.bbi.2014.06.005. Epub 2014 Jun 12.

Abstract

Both iron deficiency (ID) and infection are common during pregnancy and studies have described altered brain development in offspring as a result of these individual maternal exposures. Given their high global incidence, these two insults may occur simultaneously during pregnancy. We recently described a rat model which pairs dietary ID during pregnancy and prenatal immune activation. Pregnant rats were placed on iron sufficient (IS) or ID diets from embryonic day 2 (E2) until postnatal day 7, and administered the bacterial endotoxin, lipopolysaccharide (LPS) or saline on E15/16. In this model, LPS administration on E15 caused greater induction of the pro-inflammatory cytokines, interleukin-6 and tumor necrosis factor-α, in ID dams compared to IS dams. This suggested that the combination of prenatal immune activation on a background of maternal ID might have more adverse neurodevelopmental consequences for the offspring than exposure to either insult alone. In this study we used this model to determine whether combined exposure to maternal ID and prenatal immune activation interact to affect juvenile and adult behaviors in the offspring. We assessed behaviors relevant to deficits in humans or animals that have been associated with exposure to either maternal ID or prenatal immune activation alone. Adult offspring from ID dams displayed significant deficits in pre-pulse inhibition of acoustic startle and in passive avoidance learning, together with increases in cytochrome oxidase immunohistochemistry, a marker of metabolic activity, in the ventral hippocampus immediately after passive avoidance testing. Offspring from LPS treated dams showed a significant increase in social behavior with unfamiliar rats, and subtle locomotor changes during exploration in an open field and in response to amphetamine. Surprisingly, there was no interaction between effects of the two insults on the behaviors assessed, and few observed alterations in juvenile behavior. Our findings show that long-term effects of maternal ID and prenatal LPS were additive, such that offspring exposed to both insults displayed more adult behavioral abnormalities than offspring exposed to one alone.

摘要

缺铁(ID)和感染在怀孕期间都很常见,研究表明,由于这些母体暴露,后代的大脑发育会发生改变。鉴于它们在全球的高发病率,这两种损伤在怀孕期间可能同时发生。我们最近描述了一种在怀孕期间将饮食性缺铁和产前免疫激活相结合的大鼠模型。从胚胎第 2 天(E2)到产后第 7 天,怀孕的大鼠被置于铁充足(IS)或缺铁(ID)饮食中,并在 E15/16 给予细菌内毒素脂多糖(LPS)或生理盐水。在该模型中,与 IS 母体相比,LPS 处理在 E15 时导致 ID 母体中促炎细胞因子白细胞介素-6 和肿瘤坏死因子-α的诱导更高。这表明,在母体缺铁的背景下,产前免疫激活的组合可能对后代的神经发育后果比单独暴露于任何一种损伤更不利。在这项研究中,我们使用该模型来确定母体缺铁和产前免疫激活的联合暴露是否会相互作用,从而影响后代的青少年和成年行为。我们评估了与人类或单独暴露于母体缺铁或产前免疫激活相关的行为缺陷相关的行为。来自 ID 母体的成年后代在听觉起始惊吓的前脉冲抑制和被动回避学习中表现出明显的缺陷,并且在被动回避测试后立即在腹侧海马体中增加了细胞色素氧化酶免疫组织化学,这是代谢活性的标志物。来自 LPS 处理的母体的后代在与陌生大鼠的社交行为中表现出显著增加,并且在开放场中探索时以及对安非他命的反应中表现出微妙的运动变化。令人惊讶的是,两种损伤的影响之间没有相互作用,并且在青少年行为中观察到的变化很少。我们的研究结果表明,母体缺铁和产前 LPS 的长期影响是相加的,因此暴露于两种损伤的后代比单独暴露于一种损伤的后代表现出更多的成年行为异常。

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