Alcohol Exposure May Increase Prenatal Choline Needs Through Redirection of Choline into Lipid Synthesis Rather than Methyl Donation.

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Metabolites Pub Date : 2025-04-24 DOI:10.3390/metabo15050289
Hannah G Petry, Nipun Saini, Susan M Smith, Sandra M Mooney
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引用次数: 0

Abstract

Background: Prenatal alcohol exposure (PAE) can reduce fetal growth and cause neurodevelopmental disability. Prenatal choline supplements attenuate PAE-induced behavioral and growth deficits; however, the underlying mechanisms are unknown. Alcohol alters nutrient metabolism and potentially increases nutrient needs. Here, we investigate how alcohol affects choline metabolism in the maternal-fetal dyad and the role of supplemental choline. Methods: Pregnant C57BL/6J mice were assigned to one of four groups: alcohol-exposed (3 g/kg alcohol/day) or control +/- 100 mg/kg choline daily from embryonic day (E)8.5-17.5. We performed an exploratory hypothesis-generating analysis of targeted metabolomics on choline-related metabolites in the maternal liver, plasma, placenta, and fetal brain at E17.5 and Spearman correlation analyses to determine their association with gestational and fetal growth outcomes. Results: Although choline levels were largely unaffected by alcohol or choline, alcohol increased many lipid products in the CDP-choline pathway; this was not normalized by choline. Alcohol increased placental CDP-ethanolamine and reduced the maternal hepatic SAM/SAH ratio as well as dimethylglycine and the serine/glycine ratio across the dyad, suggesting a functional insufficiency in methyl donor pools. These outcomes were rescued by supplemental choline. Correlation analyses among choline metabolites and fetal growth outcomes suggest that maternal plasma methionine, serine, and the serine/glycine ratio may be predictive of maternal-fetal choline status. Conclusions: The increased hepatic lipid synthesis that characterizes chronic alcohol exposure may draw choline into phospholipid biosynthesis at the expense of its use as a methyl donor. We propose that PAE increases choline needs, and that its supplementation is necessary to fulfill these competing demands for lipid and methyl use.

酒精暴露可能通过将胆碱重定向到脂质合成而不是甲基捐献而增加产前胆碱需求。
背景:产前酒精暴露(PAE)可降低胎儿生长并引起神经发育障碍。产前补充胆碱可减轻pae引起的行为和生长缺陷;然而,其潜在机制尚不清楚。酒精会改变营养代谢,并可能增加营养需求。在这里,我们研究了酒精如何影响母胎双体的胆碱代谢以及补充胆碱的作用。方法:将妊娠C57BL/6J小鼠分为四组:酒精暴露组(3 g/kg酒精/d)或对照组(+/- 100 mg/kg胆碱/d),从胚胎日(E)8.5-17.5开始。我们在妊娠17.5岁时对母体肝脏、血浆、胎盘和胎儿大脑中的胆碱相关代谢物进行了探索性假设生成分析,并进行了Spearman相关分析,以确定它们与妊娠和胎儿生长结局的关系。结果:尽管胆碱水平在很大程度上不受酒精或胆碱的影响,但酒精增加了cdp -胆碱途径中的许多脂质产物;胆碱不能使其正常化。酒精增加了胎盘cdp -乙醇胺,降低了母体肝脏SAM/SAH比率以及二甲基甘氨酸和二甲基甘氨酸/甘氨酸比率,表明甲基供体池功能不足。这些结果可以通过补充胆碱来挽救。胆碱代谢物与胎儿生长结局的相关性分析表明,母体血浆蛋氨酸、丝氨酸和丝氨酸/甘氨酸比值可预测母体-胎儿胆碱状态。结论:慢性酒精暴露的特点是肝脏脂质合成增加,可能以牺牲胆碱作为甲基供体的作用为代价,将胆碱引入磷脂生物合成。我们认为PAE增加了胆碱的需求,并且它的补充是必要的,以满足脂质和甲基使用的竞争需求。
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
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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