Document Detail

Prenatal ethanol exposure has differential effects on fetal growth and skeletal ossification.
MedLine Citation:
PMID:  15777686     Owner:  NLM     Status:  MEDLINE    
There is increasing evidence suggesting that the intrauterine environment may influence long-term bone health and the risk of developing osteoporosis in later life. Alcohol (ethanol) is one factor whose presence in the prenatal environment has long-term consequences for the offspring, including permanent growth retardation. Moreover, prenatal ethanol exposure retards both fetal and postnatal bone development. It is unknown if ethanol's effects on skeletal development result from generalized growth retardation or effects specific to skeletal development. Furthermore, the level of ethanol exposure required to produce skeletal effects is unknown. The objectives of this study were to determine (1) if ethanol exerts specific effects on fetal skeletal development that are independent from its effects on general growth, and (2) the level of prenatal ethanol exposure required to affect fetal growth and skeletal ossification. Rats were fed isocaloric diets with ethanol (15%, 25%, or 36% ethanol-derived calories (EDC), approximating low, moderate, and high exposure levels), or without ethanol (pair-fed, PF, or control, C groups), prior to and throughout 21 days of gestation. The degree of E-induced delay in development was determined by comparison of E fetuses on d21 gestation to C fetuses on d17-d21 gestation. Prenatal ethanol exposure at 36% EDC decreased fetal body weight, length, and skeletal ossification compared with PF and C fetuses on d21 gestation. Importantly, effects on ossification, but not body weight or length, were also seen at the more moderate dose of 25% EDC, and the number of bones affected and the severity of effects on ossification tended to increase with dose of ethanol. Comparison of E fetuses on d21 gestation with C fetuses from d17 to 21 gestation indicated that the ethanol-induced delay in development differed for weight and skeletal ossification, and was not uniform among skeletal sites. Taken together, these data suggest that prenatal ethanol exposure has effects on fetal skeletal development that are independent of those on overall fetal growth, and that these effects occur even at moderate levels of maternal drinking. Effects of prenatal ethanol exposure on fetal skeletal development could potentially increase the offspring's risk of osteoporosis later in life.
M E Simpson; S Duggal; K Keiver
Related Documents :
14584516 - Method for quantitatively assessing physical risk factors during variable noncyclic work.
9407596 - Birth weight and congenital anomalies following poisonous mushroom intoxication during ...
16801726 - Fetal alcohol syndrome disorders: experience on the field. the lazio study preliminary ...
8520956 - Maternal pesticide exposure and pregnancy outcome.
16235296 - Cleavage stage versus blastocyst stage embryo transfer in assisted conception.
25233926 - Z-score reference ranges for normal fetal heart sizes throughout pregnancy derived from...
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Bone     Volume:  36     ISSN:  8756-3282     ISO Abbreviation:  Bone     Publication Date:  2005 Mar 
Date Detail:
Created Date:  2005-04-12     Completed Date:  2005-07-08     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8504048     Medline TA:  Bone     Country:  United States    
Other Details:
Languages:  eng     Pagination:  521-32     Citation Subset:  IM    
Food, Nutrition and Health, Faculty of Agricultural Sciences, The University of British Columbia, 2205 East Mall, Vancouver, BC, Canada.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Animals, Newborn
Bone Development / drug effects*,  physiology
Ethanol / pharmacology*
Fetal Development / drug effects*,  physiology
Osteogenesis / drug effects*,  physiology
Prenatal Exposure Delayed Effects*
Rats, Sprague-Dawley
Grant Support
Reg. No./Substance:

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

Previous Document:  Bisphosphonate (YM529) delays the repair of cortical bone defect after drill-hole injury by reducing...
Next Document:  Seroprevalence of Toxoplasma gondii in farm-reared ostriches and wild game species from Zimbabwe.