Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice.

CEBRAL E; ABREVAYA X; MUDRY MD

CELL BIOLOGY AND TOXICOLOGY

SPRINGER

Año: 2011 vol. 27 p. 1 - 12

0742-2091

Since genetic damage induced by ethanol exposure is controversial and incomplete and because germ and somatic cells constitute bioindicators for monitoring reproductive toxicity and genotoxic actions of ethanol consumption, the purpose of the present investigation was to evaluate morphological sperm, oocyte alterations and parental genotoxic effects after sub-chronic ethanol intake in the CF-1 outbred mouse strain. Ethanol 10% was administered to CF-1 adult male (treated males, TM) and female (treated females, TF) mice for 27 days, whereas water was given to controls from both sexes too (CM and CF). Post-treatment micronucleus frequency (MN-PCE/1000/mouse) and gamete morphology were evaluated. To test whether change of female reproductive status results in maternal genotoxicity, CF-1 females received ethanol 10% (exposed group, PTF) or water (control group, PCF) in drinking water for 17 days previous and up to 10 days of gestation. TM had a high percentage of abnormal spermatozoa vs CM (p<0.001) and elevated parthenogenetic activated oocyte frequency appeared in TF vs CF (p<0.001). Sub-chronic ethanol ingestion induced increased MN frequency in TM and TF (p<0.01). In periconceptionally treated females (PTF), where blood alcohol concentrations were between 19-28 mg/dl, very significantly increased MN frequency was found vs PCF (p<0.01), whereas MN values were similar to TF. These results show that sub-chronic alcohol ingestion in CF-1 mice produces sperm head dysmorphogenesis and oocyte nuclear anomalies, suggesting that morphological abnormalities in germ cells are probably related to parental genotoxicity after ethanol consumption.