Document Detail


Early exposure to ethanol but not red wine at the same alcohol concentration induces behavioral and brain neurotrophin alterations in young and adult mice.
MedLine Citation:
PMID:  19100286     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Ethanol exposure during pregnancy is one of the major causes of mental retardation in western countries by inducing fetal-alcohol-like-syndromes. Red wine is known to contain ethanol but also compounds with putative antioxidant properties. It has also been shown that nerve growth factor (NGF) and brain derived neurotrophic factor (BDNF) are severely affected by ethanol during prenatal and postnatal life. The aim of the current study was to investigate in male CD1 mice brain alterations in NGF and BDNF due to chronic early exposure to ethanol solution (11 vol%) or to red wine at the same alcohol concentration starting from 60 days before pregnancy up to pups weaning. Data revealed no differences between groups of dams in pregnancy duration, neither in pups delivery, pups mortality and sex ratio. Data also showed that adult animals exposed to only ethanol had disrupted levels of both NGF and BDNF in the hippocampus and other brain areas. This profile was associated with impaired ChAT immunopositivity in the septum and Nuclei Basalis and with altered cognition and emotional behavior. Quite interestingly mice exposed to red wine had no change in the behavior or in ChAT immunopositivity but a decrease in hippocampal BDNF and a mild NGF decrease in the cortex. Also NGF-induced neuritic outgrowth in PC-12 cells was still present when exposed to red wine but not when exposed to ethanol solution only. Data suggest differences in ethanol-induced neurotoxicity between red wine and ethanol solution only.
Authors:
Marco Fiore; Giovanni Laviola; Luigi Aloe; Veronica di Fausto; Rosanna Mancinelli; Mauro Ceccanti
Related Documents :
1680076 - Peripartum cocaine use: estimating risk of adverse pregnancy outcome.
19541806 - Maternal occupational exposure to solvents and congenital malformations: a prospective ...
18498046 - Alcohol use, injuries, and prenatal visits during three successive pregnancies among am...
17439336 - Limits of usual biochemical alcohol markers in cord blood at term: a fetal/maternal pop...
2130676 - Ultrasound diagnosis and screening of fetal cystic fibrosis.
15280906 - Pulque intake during pregnancy and lactation in rural mexico: alcohol and child growth ...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-11-28
Journal Detail:
Title:  Neurotoxicology     Volume:  30     ISSN:  0161-813X     ISO Abbreviation:  Neurotoxicology     Publication Date:  2009 Jan 
Date Detail:
Created Date:  2009-01-26     Completed Date:  2009-04-13     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7905589     Medline TA:  Neurotoxicology     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  59-71     Citation Subset:  IM    
Affiliation:
Istituto di Neurobiologia e Medicina Molecolare, Via del Fosso di Fiorano 64, 00143 Roma, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Behavior, Animal / drug effects
Body Weight / drug effects*
Brain / anatomy & histology,  drug effects*,  metabolism*,  physiology
Brain-Derived Neurotrophic Factor / metabolism*
Choline O-Acetyltransferase / analysis
Cognition / drug effects
Emotions / drug effects
Ethanol / administration & dosage,  blood,  toxicity*
Female
Male
Maternal-Fetal Exchange*
Mice
Nerve Growth Factor / metabolism*
Pregnancy
Wine / adverse effects
Chemical
Reg. No./Substance:
0/Brain-Derived Neurotrophic Factor; 64-17-5/Ethanol; 9061-61-4/Nerve Growth Factor; EC 2.3.1.6/Choline O-Acetyltransferase

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


Previous Document:  The RepA_N replicons of Gram-positive bacteria: a family of broadly distributed but narrow host rang...
Next Document:  Long-term cognitive deficits accompanied by reduced neurogenesis after soman poisoning.