Postnatal growth restriction and gene expression changes in a mouse model of fetal alcohol syndrome

✍ Scribed by Nina Kaminen-Ahola; Arttu Ahola; Traute Flatscher-Bader; Sarah J. Wilkins; Greg J. Anderson; Emma Whitelaw; Suyinn Chong

• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 311 KB
• Volume: 88
• Category: Article
• ISSN: 1542-0752
• DOI: 10.1002/bdra.20729

✦ Synopsis

Abstract

Growth restriction, craniofacial dysmorphology, and central nervous system defects are the main diagnostic features of fetal alcohol syndrome. Studies in humans and mice have reported that the growth restriction can be prenatal or postnatal, but the underlying mechanisms remain unknown.

We recently described a mouse model of moderate gestational ethanol exposure that produces measurable phenotypes in line with fetal alcohol syndrome (e.g., craniofacial changes and growth restriction in adolescent mice). In this study, we characterize in detail the growth restriction phenotype by measuring body weight at gestational day 16.5, cross‐fostering from birth to weaning, and by extending our observations into adulthood. Furthermore, in an attempt to unravel the molecular events contributing to the growth phenotype, we have compared gene expression patterns in the liver and kidney of nonfostered, ethanol‐exposed and control mice at postnatal day 28.

We find that the ethanol‐induced growth phenotype is not detectable prior to birth, but is present at weaning, even in mice that have been cross‐fostered to unexposed dams. This finding suggests a postnatal growth restriction phenotype that is not due to deficient postpartum care by dams that drank ethanol, but rather a physiologic result of ethanol exposure in utero. We also find that, despite some catch‐up growth after 5 weeks of age, the effect extends into adulthood, which is consistent with longitudinal studies in humans.

Genome‐wide gene expression analysis revealed interesting ethanol‐induced changes in the liver, including genes involved in the metabolism of exogenous and endogenous compounds, iron homeostasis, and lipid metabolism. Birth Defects Research (Part A), 2010. © 2010 Wiley‐Liss, Inc.