Document Detail


Genesis of alcohol-induced craniofacial dysmorphism.
MedLine Citation:
PMID:  15956766     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The initial diagnosis of fetal alcohol syndrome (FAS) in the United States was made because of the facial features common to the first cohort of patients. This article reviews the development of an FAS mouse model whose craniofacial features are remarkably similar to those of affected humans. The model is based on short-term maternal treatment with a high dosage of ethanol at stages of pregnancy that are equivalent to Weeks 3 and 4 of human gestation. At these early stages of development, alcohol's insult to the developing face is concurrent with that to the brain, eyes, and inner ear. That facial and central nervous system defects consistent with FAS can be induced by more "realistic" alcohol dosages as illustrated with data from an oral alcohol intake mouse model in which maternal blood alcohol levels do not exceed 200 mg/dl. The ethanol-induced pathogenesis involves apoptosis that occurs within 12 hrs of alcohol exposure in selected cell populations of Day 7, 8, and 9 mouse embryos. Experimental evidence from other species also shows that apoptosis underlies ethanol-induced malformations. With knowledge of sensitive and resistant cell populations at specific developmental stages, studies designed to identify the basis for these differing cellular responses and, therefore, to determine the primary mechanisms of ethanol's teratogenesis are possible. For example, microarray comparisons of sensitive and resistant embryonic cell populations have been made, as have in situ studies of gene expression patterns in the populations of interest. Studies that illustrate agents that are effective in diminishing or exacerbating ethanol's teratogenesis have also been helpful in determining mechanisms. Among these agents are antioxidants, sonic hedgehog protein, retinoids, and the peptides SAL and NAP.
Authors:
Kathleen K Sulik
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Experimental biology and medicine (Maywood, N.J.)     Volume:  230     ISSN:  1535-3702     ISO Abbreviation:  Exp. Biol. Med. (Maywood)     Publication Date:  2005 Jun 
Date Detail:
Created Date:  2005-06-15     Completed Date:  2005-07-18     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  100973463     Medline TA:  Exp Biol Med (Maywood)     Country:  United States    
Other Details:
Languages:  eng     Pagination:  366-75     Citation Subset:  IM    
Affiliation:
Department of Cell and Developmental Biology and Bowles Center for Alcohol Studies, The University of North Carolina, CB 7090, Chapel Hill, North Carolina 27599, USA. mouse@camed.unc.edu
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MeSH Terms
Descriptor/Qualifier:
Alcohol Drinking / adverse effects*
Animals
Brain / abnormalities,  drug effects,  ultrastructure
Craniofacial Abnormalities / embryology,  etiology*,  pathology
Disease Models, Animal
Embryo, Mammalian / ultrastructure
Eye Abnormalities / embryology,  etiology
Female
Fetal Alcohol Syndrome / embryology,  etiology*,  pathology
Gestational Age
Humans
Maxillofacial Development / drug effects
Mice
Pregnancy

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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