Affiliation:
1. Bowles Center for Alcohol Studies The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA
2. Department of Neuroscience and Physiology SUNY Upstate Medical University Syracuse NY USA
3. Carolina Institute for Developmental Disabilities The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA
4. UNC Neuroscience Center University of North Carolina at Chapel Hill Chapel Hill North Carolina USA
5. Department of Genetics The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA
6. Department of Cell Biology and Physiology The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA
Abstract
AbstractBackgroundPrenatal alcohol exposure during gastrulation (embryonic day [E] 7 in mice, ~3rd week of human pregnancy) impairs eye, facial, and cortical development, recapitulating birth defects characteristic of Fetal Alcohol Syndrome (FAS). However, it is not known whether the prevalence or severity of craniofacial features associated with FAS is affected by biological sex.MethodsThe current study administered either alcohol (2.9 g/kg, two i.p. doses, 4 hr apart) or vehicle to pregnant C57BL/6J females on E7, prior to gonadal sex differentiation, and assessed fetal morphology at E17.ResultsWhereas sex did not affect fetal size in controls, alcohol‐exposed females were smaller than both control females and alcohol‐treated males. Alcohol exposure increased the incidence of eye defects to a similar degree in males and females. Together, these data suggest that females might be more sensitive to the general developmental effects of alcohol, but not effects specific to the craniofacies. Whole transcriptomic analysis of untreated E7 embryos found 214 differentially expressed genes in females vs. males, including those in pathways related to cilia and mitochondria, histone demethylase activity, and pluripotency.ConclusionGastrulation‐stage alcohol induces craniofacial malformations in male and female mouse fetuses at similar rates and severity, though growth deficits are more prevalent females. These findings support the investigation of biological sex as a contributing factor in prenatal alcohol studies.
Funder
Eunice Kennedy Shriver National Institute of Child Health and Human Development
National Institute of Neurological Disorders and Stroke
National Institute on Alcohol Abuse and Alcoholism
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献