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spelling paper:paper_07422091_v27_n4_p237_Cebral2023-06-08T15:44:42Z Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice Cebral, Elisa Abrevaya, Ximena Celeste Mudry, Marta Dolores CF-1 mice Ethanol Micronucleus Oocyte Spermatozoa alcohol adult animal alcohol blood level alcohol consumption animal cell animal experiment animal model article cell activation cell damage cell nucleus cell structure CF1 mouse conception controlled study cytotoxicity female gamete genotoxicity gestation period male micronucleus mouse mouse strain nonhuman oocyte priority journal reproductive toxicity sperm Alcohol Drinking Animals Ethanol Female Male Mice Mice, Inbred Strains Micronuclei, Chromosome-Defective Mutagenicity Tests Oocytes Pregnancy Reproduction Spermatozoa Mus 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/1,000/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, periconceptionally treated females (PTF)) or water (control group, pregnant control females (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 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. © 2011 Springer Science+Business Media B.V. Fil:Cebral, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Abrevaya, X.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Mudry, M.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07422091_v27_n4_p237_Cebral http://hdl.handle.net/20.500.12110/paper_07422091_v27_n4_p237_Cebral
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic CF-1 mice
Ethanol
Micronucleus
Oocyte
Spermatozoa
alcohol
adult animal
alcohol blood level
alcohol consumption
animal cell
animal experiment
animal model
article
cell activation
cell damage
cell nucleus
cell structure
CF1 mouse
conception
controlled study
cytotoxicity
female
gamete
genotoxicity
gestation period
male
micronucleus
mouse
mouse strain
nonhuman
oocyte
priority journal
reproductive toxicity
sperm
Alcohol Drinking
Animals
Ethanol
Female
Male
Mice
Mice, Inbred Strains
Micronuclei, Chromosome-Defective
Mutagenicity Tests
Oocytes
Pregnancy
Reproduction
Spermatozoa
Mus
spellingShingle CF-1 mice
Ethanol
Micronucleus
Oocyte
Spermatozoa
alcohol
adult animal
alcohol blood level
alcohol consumption
animal cell
animal experiment
animal model
article
cell activation
cell damage
cell nucleus
cell structure
CF1 mouse
conception
controlled study
cytotoxicity
female
gamete
genotoxicity
gestation period
male
micronucleus
mouse
mouse strain
nonhuman
oocyte
priority journal
reproductive toxicity
sperm
Alcohol Drinking
Animals
Ethanol
Female
Male
Mice
Mice, Inbred Strains
Micronuclei, Chromosome-Defective
Mutagenicity Tests
Oocytes
Pregnancy
Reproduction
Spermatozoa
Mus
Cebral, Elisa
Abrevaya, Ximena Celeste
Mudry, Marta Dolores
Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice
topic_facet CF-1 mice
Ethanol
Micronucleus
Oocyte
Spermatozoa
alcohol
adult animal
alcohol blood level
alcohol consumption
animal cell
animal experiment
animal model
article
cell activation
cell damage
cell nucleus
cell structure
CF1 mouse
conception
controlled study
cytotoxicity
female
gamete
genotoxicity
gestation period
male
micronucleus
mouse
mouse strain
nonhuman
oocyte
priority journal
reproductive toxicity
sperm
Alcohol Drinking
Animals
Ethanol
Female
Male
Mice
Mice, Inbred Strains
Micronuclei, Chromosome-Defective
Mutagenicity Tests
Oocytes
Pregnancy
Reproduction
Spermatozoa
Mus
description 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/1,000/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, periconceptionally treated females (PTF)) or water (control group, pregnant control females (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 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. © 2011 Springer Science+Business Media B.V.
author Cebral, Elisa
Abrevaya, Ximena Celeste
Mudry, Marta Dolores
author_facet Cebral, Elisa
Abrevaya, Ximena Celeste
Mudry, Marta Dolores
author_sort Cebral, Elisa
title Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice
title_short Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice
title_full Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice
title_fullStr Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice
title_full_unstemmed Male and female reproductive toxicity induced by sub-chronic ethanol exposure in CF-1 mice
title_sort male and female reproductive toxicity induced by sub-chronic ethanol exposure in cf-1 mice
publishDate 2011
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07422091_v27_n4_p237_Cebral
http://hdl.handle.net/20.500.12110/paper_07422091_v27_n4_p237_Cebral
work_keys_str_mv AT cebralelisa maleandfemalereproductivetoxicityinducedbysubchronicethanolexposureincf1mice
AT abrevayaximenaceleste maleandfemalereproductivetoxicityinducedbysubchronicethanolexposureincf1mice
AT mudrymartadolores maleandfemalereproductivetoxicityinducedbysubchronicethanolexposureincf1mice
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