Mitigating the detrimental developmental impact of early fetal alcohol exposure using a maternal methyl donor‐enriched diet

Author:

Breton‐Larrivée Mélanie12,Elder Elizabeth12,Legault Lisa‐Marie12,Langford‐Avelar Alexandra12,MacFarlane Amanda J.34,McGraw Serge125ORCID

Affiliation:

1. Centre Hospitalier Universitaire Sainte‐Justine Research Center Montreal Canada

2. Department of Biochemistry and Molecular Medicine Université de Montréal Montreal Canada

3. Agriculture, Food, and Nutrition Evidence Center Texas A&M University Texas Fort Worth USA

4. Department of Nutrition Texas A&M University College Station Texas USA

5. Department of Obstetrics and Gynecology Université de Montréal Montreal Canada

Abstract

AbstractFetal alcohol exposure at any stage of pregnancy can lead to fetal alcohol spectrum disorder (FASD), a group of life‐long conditions characterized by congenital malformations, as well as cognitive, behavioral, and emotional impairments. The teratogenic effects of alcohol have long been publicized; yet fetal alcohol exposure is one of the most common preventable causes of birth defects. Currently, alcohol abstinence during pregnancy is the best and only way to prevent FASD. However, alcohol consumption remains astoundingly prevalent among pregnant women; therefore, additional measures need to be made available to help protect the developing embryo before irreparable damage is done. Maternal nutritional interventions using methyl donors have been investigated as potential preventative measures to mitigate the adverse effects of fetal alcohol exposure. Here, we show that a single acute preimplantation (E2.5; 8‐cell stage) fetal alcohol exposure (2 × 2.5 g/kg ethanol with a 2h interval) in mice leads to long‐term FASD‐like morphological phenotypes (e.g. growth restriction, brain malformations, skeletal delays) in late‐gestation embryos (E18.5) and demonstrate that supplementing the maternal diet with a combination of four methyl donor nutrients, folic acid, choline, betaine, and vitamin B12, prior to conception and throughout gestation effectively reduces the incidence and severity of alcohol‐induced morphological defects without altering DNA methylation status of imprinting control regions and regulation of associated imprinted genes. This study clearly supports that preimplantation embryos are vulnerable to the teratogenic effects of alcohol, emphasizes the dangers of maternal alcohol consumption during early gestation, and provides a potential proactive maternal nutritional intervention to minimize FASD progression, reinforcing the importance of adequate preconception and prenatal nutrition.

Funder

Sick Kids Foundation

Universidad de Medellín

Canadian Institutes of Health Research

Fonds de Recherche du Québec - Santé

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

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