Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis

The placenta plays a major role in embryo-fetal defects and intrauterine growth retardation after maternal alcohol consumption. Our aims were to determine the oxidative status and cellular and molecular oxidative stress effects on uterine myometrium and trophoblast-decidual tissue following perigest...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado: 2018
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008177_v440_n1-2_p89_Coll
http://hdl.handle.net/20.500.12110/paper_03008177_v440_n1-2_p89_Coll
Aporte de:
id paper:paper_03008177_v440_n1-2_p89_Coll
record_format dspace
spelling paper:paper_03008177_v440_n1-2_p89_Coll2023-06-08T15:27:28Z Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis Cellular and tissue damage Decidua Mouse organogenesis Oxidative stress Perigestational alcohol Placenta 3 nitrotyrosine alcohol catalase drinking water glutathione glutathione transferase nitrite superoxide dismutase thiobarbituric acid reactive substance adult alcohol consumption animal experiment animal model animal tissue apoptosis Article cell nucleus controlled study decidua endothelium enzyme activity female giant cell histopathology immunohistochemistry immunoreactivity macromolecule morphometry mouse myometrium nidation nonhuman organogenesis oxidative stress pregnancy trophoblast animal decidua fetal alcohol syndrome maternal exposure metabolism myometrium pathology pregnancy trophoblast Animals Decidua Female Fetal Alcohol Spectrum Disorders Maternal Exposure Mice Myometrium Organogenesis Oxidative Stress Pregnancy Trophoblasts The placenta plays a major role in embryo-fetal defects and intrauterine growth retardation after maternal alcohol consumption. Our aims were to determine the oxidative status and cellular and molecular oxidative stress effects on uterine myometrium and trophoblast-decidual tissue following perigestational alcohol intake at early organogenesis. CF-1 female mice were administered with 10% alcohol in drinking water for 17 days prior to and up to day 10 of gestation. Control females received ethanol-free water. Treated mice had smaller implantation sites compared to controls (p < 0.05), diminished maternal vascular lumen, and irregular/discontinuous endothelium of decidual vessels. The trophoblast giant cell layer was disorganized and presented increased abnormal nuclear frequency. The myometrium of treated females had reduced nitrite content, increased superoxide dismutase activity, and reduced glutathione (GSH) content (p < 0.05). However, the trophoblast-decidual tissue of treated females had increased nitrite content (p < 0.05), increased GSH level (p < 0.001), increased thiobarbituric acid-reactive substance concentration (p < 0.001), higher 3-nitrotyrosine immunoreaction, and increased apoptotic index (p < 0.05) compared to controls. In summary, perigestational alcohol ingestion at organogenesis induced oxidative stress in the myometrium and trophoblast-decidual tissue, mainly affecting cells and macromolecules of trophoblast and decidual tissues around early organogenesis, in CF-1 mouse, and suggests that oxidative-induced abnormal early placental formation probably leads to risk of prematurity and fetal growth impairment at term. © 2017, Springer Science+Business Media, LLC. 2018 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008177_v440_n1-2_p89_Coll http://hdl.handle.net/20.500.12110/paper_03008177_v440_n1-2_p89_Coll
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cellular and tissue damage
Decidua
Mouse organogenesis
Oxidative stress
Perigestational alcohol
Placenta
3 nitrotyrosine
alcohol
catalase
drinking water
glutathione
glutathione transferase
nitrite
superoxide dismutase
thiobarbituric acid reactive substance
adult
alcohol consumption
animal experiment
animal model
animal tissue
apoptosis
Article
cell nucleus
controlled study
decidua
endothelium
enzyme activity
female
giant cell
histopathology
immunohistochemistry
immunoreactivity
macromolecule
morphometry
mouse
myometrium
nidation
nonhuman
organogenesis
oxidative stress
pregnancy
trophoblast
animal
decidua
fetal alcohol syndrome
maternal exposure
metabolism
myometrium
pathology
pregnancy
trophoblast
Animals
Decidua
Female
Fetal Alcohol Spectrum Disorders
Maternal Exposure
Mice
Myometrium
Organogenesis
Oxidative Stress
Pregnancy
Trophoblasts
spellingShingle Cellular and tissue damage
Decidua
Mouse organogenesis
Oxidative stress
Perigestational alcohol
Placenta
3 nitrotyrosine
alcohol
catalase
drinking water
glutathione
glutathione transferase
nitrite
superoxide dismutase
thiobarbituric acid reactive substance
adult
alcohol consumption
animal experiment
animal model
animal tissue
apoptosis
Article
cell nucleus
controlled study
decidua
endothelium
enzyme activity
female
giant cell
histopathology
immunohistochemistry
immunoreactivity
macromolecule
morphometry
mouse
myometrium
nidation
nonhuman
organogenesis
oxidative stress
pregnancy
trophoblast
animal
decidua
fetal alcohol syndrome
maternal exposure
metabolism
myometrium
pathology
pregnancy
trophoblast
Animals
Decidua
Female
Fetal Alcohol Spectrum Disorders
Maternal Exposure
Mice
Myometrium
Organogenesis
Oxidative Stress
Pregnancy
Trophoblasts
Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
topic_facet Cellular and tissue damage
Decidua
Mouse organogenesis
Oxidative stress
Perigestational alcohol
Placenta
3 nitrotyrosine
alcohol
catalase
drinking water
glutathione
glutathione transferase
nitrite
superoxide dismutase
thiobarbituric acid reactive substance
adult
alcohol consumption
animal experiment
animal model
animal tissue
apoptosis
Article
cell nucleus
controlled study
decidua
endothelium
enzyme activity
female
giant cell
histopathology
immunohistochemistry
immunoreactivity
macromolecule
morphometry
mouse
myometrium
nidation
nonhuman
organogenesis
oxidative stress
pregnancy
trophoblast
animal
decidua
fetal alcohol syndrome
maternal exposure
metabolism
myometrium
pathology
pregnancy
trophoblast
Animals
Decidua
Female
Fetal Alcohol Spectrum Disorders
Maternal Exposure
Mice
Myometrium
Organogenesis
Oxidative Stress
Pregnancy
Trophoblasts
description The placenta plays a major role in embryo-fetal defects and intrauterine growth retardation after maternal alcohol consumption. Our aims were to determine the oxidative status and cellular and molecular oxidative stress effects on uterine myometrium and trophoblast-decidual tissue following perigestational alcohol intake at early organogenesis. CF-1 female mice were administered with 10% alcohol in drinking water for 17 days prior to and up to day 10 of gestation. Control females received ethanol-free water. Treated mice had smaller implantation sites compared to controls (p < 0.05), diminished maternal vascular lumen, and irregular/discontinuous endothelium of decidual vessels. The trophoblast giant cell layer was disorganized and presented increased abnormal nuclear frequency. The myometrium of treated females had reduced nitrite content, increased superoxide dismutase activity, and reduced glutathione (GSH) content (p < 0.05). However, the trophoblast-decidual tissue of treated females had increased nitrite content (p < 0.05), increased GSH level (p < 0.001), increased thiobarbituric acid-reactive substance concentration (p < 0.001), higher 3-nitrotyrosine immunoreaction, and increased apoptotic index (p < 0.05) compared to controls. In summary, perigestational alcohol ingestion at organogenesis induced oxidative stress in the myometrium and trophoblast-decidual tissue, mainly affecting cells and macromolecules of trophoblast and decidual tissues around early organogenesis, in CF-1 mouse, and suggests that oxidative-induced abnormal early placental formation probably leads to risk of prematurity and fetal growth impairment at term. © 2017, Springer Science+Business Media, LLC.
title Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
title_short Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
title_full Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
title_fullStr Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
title_full_unstemmed Cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
title_sort cellular and molecular oxidative stress-related effects in uterine myometrial and trophoblast-decidual tissues after perigestational alcohol intake up to early mouse organogenesis
publishDate 2018
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008177_v440_n1-2_p89_Coll
http://hdl.handle.net/20.500.12110/paper_03008177_v440_n1-2_p89_Coll
_version_ 1768544911585443840