Unraveling the Molecular Mechanisms of the Neurodevelopmental Consequences of Fetal Protein Deficiency: Insights From Rodent Models and Public Health Implications

IF 4 Q2 NEUROSCIENCES
Pieter Vancamp , Morgane Frapin , Patricia Parnet , Valérie Amarger
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Abstract

Fetal brain development requires increased maternal protein intake to ensure that offspring reach their optimal cognitive potential in infancy and adulthood. While protein deficiency remains a prevalent issue in developing countries, it is also reemerging in Western societies due to the growing adoption of plant-based diets, some of which are monotonous and may fail to provide sufficient amino acids crucial for the brain’s critical developmental phase. Confounding variables in human nutritional research have impeded our understanding of the precise impact of protein deficiency on fetal neurodevelopment, as well as its implications for childhood neurocognitive performance. Moreover, it remains unclear whether such deficiency could predispose to mental health problems in adulthood, mirroring observations in individuals exposed to prenatal famine. In this review, we sought to evaluate mechanistic data derived from rodent models, placing special emphasis on the involvement of neuroendocrine axes, the influence of sex and timing, epigenetic modifications, and cellular metabolism. Despite notable progress, critical knowledge gaps remain, including understanding the long-term reversibility of effects due to fetal protein restriction and the interplay between genetic predisposition and environmental factors. Enhancing our understanding of the precise mechanisms that connect prenatal nutrition to brain development in future research endeavors can be significantly advanced by integrating multiomics approaches and utilizing additional alternative models such as nonhuman primates. Furthermore, it is crucial to investigate potential interventions aimed at alleviating adverse outcomes. Ultimately, this research has profound implications for guiding public health strategies aimed at raising awareness about the crucial role of optimal maternal nutrition in supporting fetal neurodevelopment.

揭示胎儿蛋白质缺乏症对神经发育影响的分子机制:啮齿动物模型的启示和对公共卫生的影响。
胎儿的大脑发育需要母体摄入更多的蛋白质,以确保后代在婴儿期和成年期达到最佳认知潜能。虽然蛋白质缺乏症在发展中国家仍是一个普遍问题,但由于西方社会越来越多地采用植物性饮食,蛋白质缺乏症在西方社会也再次出现,因为有些植物性饮食比较单调,可能无法提供足够的对大脑关键发育阶段至关重要的氨基酸。人类营养研究中的干扰变量阻碍了我们了解蛋白质缺乏对胎儿神经发育的确切影响及其对儿童神经认知表现的影响。此外,这种蛋白质缺乏是否会导致成年后出现心理健康问题,这与在产前遭受饥荒的个体身上观察到的情况如出一辙,目前仍不清楚。在这篇综述中,我们试图评估从啮齿动物模型中获得的机理数据,特别强调神经内分泌轴的参与、性别和时间的影响、表观遗传修饰和细胞代谢。尽管取得了显著进展,但仍存在关键的知识差距,包括了解胎儿蛋白质限制所造成影响的长期可逆性,以及遗传易感性和环境因素之间的相互作用。在未来的研究工作中,通过整合多组学方法和利用更多的替代模型(如非人灵长类动物),可以极大地促进我们对产前营养与大脑发育之间确切联系机制的理解。此外,研究旨在减轻不良后果的潜在干预措施也至关重要。最终,这项研究对指导公共卫生策略具有深远的意义,旨在提高人们对最佳母体营养在支持胎儿神经发育中的关键作用的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
CiteScore
4.00
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91 days
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