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早期生活中的铁缺乏会持续破坏小鼠的情感行为。

Early-life iron deficiency persistently disrupts affective behaviour in mice.

机构信息

Department of Neurophysiology and Neuropharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.

出版信息

Ann Med. 2023 Dec;55(1):1265-1277. doi: 10.1080/07853890.2023.2191003.

Abstract

BACKGROUND/OBJECTIVE: Iron deficiency (ID) is the most common nutrient deficiency, affecting two billion people worldwide, including about 30% of pregnant women. During gestation, the brain is particularly vulnerable to environmental insults, which can irrevocably impair critical developmental processes. Consequently, detrimental consequences of early-life ID for offspring brain structure and function have been described. Although early life ID has been associated with an increased long-term risk for several neuropsychiatric disorders, the effect on depressive disorders has remained unresolved.

MATERIALS AND METHODS

A mouse model of moderate foetal and neonatal ID was established by keeping pregnant dams on an iron-deficient diet throughout gestation until postnatal day 10. The ensuing significant decrease of iron content in the offspring brain, as well as the impact on maternal behaviour and offspring vocalization was determined in the first postnatal week. The consequences of early-life ID for depression- and anxiety-like behaviour in adulthood were revealed employing dedicated behavioural assays. miRNA sequencing of hippocampal tissue of offspring revealed specific miRNAs signatures accompanying the behavioural deficits of foetal and neonatal ID in the adult brain.

RESULTS

Mothers receiving iron-deficient food during pregnancy and lactation exhibited significantly less licking and grooming behaviour, while active pup retrieval and pup ultrasonic vocalizations were unaltered. Adult offspring with a history of foetal and neonatal ID showed an increase in depression- and anxiety-like behaviour, paralleled by a deranged miRNA expression profile in the hippocampus, specifically levels of miR200a and miR200b.

CONCLUSION

ID during the foetal and neonatal periods has life-long consequences for affective behaviour in mice and leaves a specific and persistent mark on the expression of miRNAs in the brain. Foetal and neonatal ID needs to be further considered as risk factor for the development of depression and anxiety disorders later in life.Key MessagesMarginal reduction of gestational alimentary iron intake decreases brain iron content of the juvenile offspring.Early-life ID is associated with increased depression- and anxiety-like behaviour in adulthood.Reduction of maternal alimentary iron intake during pregnancy is reflected in an alteration of miRNA signatures in the adult offspring brain.

摘要

背景/目的:铁缺乏(ID)是最常见的营养缺乏症,影响着全球 20 亿人,其中包括约 30%的孕妇。在妊娠期间,大脑特别容易受到环境损伤的影响,这可能会不可逆转地损害关键的发育过程。因此,已经描述了生命早期 ID 对后代大脑结构和功能的不利后果。尽管生命早期 ID 与几种神经精神疾病的长期风险增加有关,但对抑郁症的影响仍未得到解决。

材料和方法

通过让怀孕的母鼠在整个妊娠期和产后第 10 天一直食用缺铁饮食,建立了一种中度胎儿和新生儿 ID 的小鼠模型。在出生后的第一周,确定了后代大脑中铁含量的显著下降,以及对母体行为和后代发声的影响。采用专门的行为测定法揭示了生命早期 ID 对成年期抑郁和焦虑样行为的影响。对后代海马组织的 miRNA 测序揭示了伴随着胎儿和新生儿 ID 在成年大脑中出现行为缺陷的特定 miRNA 特征。

结果

怀孕期间和哺乳期接受缺铁饮食的母亲表现出明显较少的舔舐和梳理行为,而主动取幼仔和幼仔超声波发声则没有改变。有胎儿和新生儿 ID 病史的成年后代表现出抑郁和焦虑样行为增加,同时海马中 miRNA 表达谱失调,特别是 miR200a 和 miR200b 的水平。

结论

胎儿和新生儿期的 ID 对小鼠的情感行为有终身影响,并在大脑中 miRNA 的表达上留下特定且持久的印记。胎儿和新生儿 ID 需要进一步被视为日后发展为抑郁症和焦虑症的风险因素。

关键信息

妊娠期饮食铁摄入量的轻微减少会降低幼年后代的大脑铁含量。生命早期 ID 与成年后抑郁和焦虑样行为增加有关。怀孕期间饮食铁摄入量的减少反映在成年后代大脑中 miRNA 特征的改变。

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