Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes

Maternal diabetes programs cardiovascular alterations in the adult offspring but the mechanisms involved remain unclarified. Here, we addresed whether maternal diabetes programs cardiac alterations related to extracellular matrix remodeling in the adult offspring, as well as the role of forkhead box...

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Publicado: 2019
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rat
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03037207_v479_n_p78_Musikant
http://hdl.handle.net/20.500.12110/paper_03037207_v479_n_p78_Musikant
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spelling paper:paper_03037207_v479_n_p78_Musikant2023-06-08T15:29:13Z Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes Connexin43 Diabetes FOXO1 Heart Intrauterine programming Matrix metalloproteinases collagen connexin 43 messenger RNA streptozocin transcription factor FKHR adult animal experiment animal model animal tissue Article cardiomyopathy cardiovascular parameters controlled study Ctgf gene enzyme activation extracellular matrix female gene gene targeting heart hyperglycemia hypertriglyceridemia insulinemia male maternal diabetes mellitus Mmp 2 gene nonhuman pathogenesis priority journal progeny protein function rat Maternal diabetes programs cardiovascular alterations in the adult offspring but the mechanisms involved remain unclarified. Here, we addresed whether maternal diabetes programs cardiac alterations related to extracellular matrix remodeling in the adult offspring, as well as the role of forkhead box transcription factor 1 (FOXO1) in the induction of these alterations. The heart from adult offspring from control and streptozotocin-induced diabetic rats was evaluated. Increased glycemia, triglyceridemia and insulinemia and markers of cardiomyopathy were found in the offspring from diabetic rats. In the heart, an increase in active FOXO1 and mRNA levels of its target genes, Mmp-2 and Ctgf, genes related to an altered extracellular matrix remodeling, together with an increase in collagen deposition and a decrease in the connexin43 levels, were found in the offspring from diabetic rats. Altogether, these results suggest an important role of FOXO1 activation in the cardiac alterations induced by intrauterine programming in maternal diabetes. © 2018 2019 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03037207_v479_n_p78_Musikant http://hdl.handle.net/20.500.12110/paper_03037207_v479_n_p78_Musikant
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Connexin43
Diabetes
FOXO1
Heart
Intrauterine programming
Matrix metalloproteinases
collagen
connexin 43
messenger RNA
streptozocin
transcription factor FKHR
adult
animal experiment
animal model
animal tissue
Article
cardiomyopathy
cardiovascular parameters
controlled study
Ctgf gene
enzyme activation
extracellular matrix
female
gene
gene targeting
heart
hyperglycemia
hypertriglyceridemia
insulinemia
male
maternal diabetes mellitus
Mmp 2 gene
nonhuman
pathogenesis
priority journal
progeny
protein function
rat
spellingShingle Connexin43
Diabetes
FOXO1
Heart
Intrauterine programming
Matrix metalloproteinases
collagen
connexin 43
messenger RNA
streptozocin
transcription factor FKHR
adult
animal experiment
animal model
animal tissue
Article
cardiomyopathy
cardiovascular parameters
controlled study
Ctgf gene
enzyme activation
extracellular matrix
female
gene
gene targeting
heart
hyperglycemia
hypertriglyceridemia
insulinemia
male
maternal diabetes mellitus
Mmp 2 gene
nonhuman
pathogenesis
priority journal
progeny
protein function
rat
Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes
topic_facet Connexin43
Diabetes
FOXO1
Heart
Intrauterine programming
Matrix metalloproteinases
collagen
connexin 43
messenger RNA
streptozocin
transcription factor FKHR
adult
animal experiment
animal model
animal tissue
Article
cardiomyopathy
cardiovascular parameters
controlled study
Ctgf gene
enzyme activation
extracellular matrix
female
gene
gene targeting
heart
hyperglycemia
hypertriglyceridemia
insulinemia
male
maternal diabetes mellitus
Mmp 2 gene
nonhuman
pathogenesis
priority journal
progeny
protein function
rat
description Maternal diabetes programs cardiovascular alterations in the adult offspring but the mechanisms involved remain unclarified. Here, we addresed whether maternal diabetes programs cardiac alterations related to extracellular matrix remodeling in the adult offspring, as well as the role of forkhead box transcription factor 1 (FOXO1) in the induction of these alterations. The heart from adult offspring from control and streptozotocin-induced diabetic rats was evaluated. Increased glycemia, triglyceridemia and insulinemia and markers of cardiomyopathy were found in the offspring from diabetic rats. In the heart, an increase in active FOXO1 and mRNA levels of its target genes, Mmp-2 and Ctgf, genes related to an altered extracellular matrix remodeling, together with an increase in collagen deposition and a decrease in the connexin43 levels, were found in the offspring from diabetic rats. Altogether, these results suggest an important role of FOXO1 activation in the cardiac alterations induced by intrauterine programming in maternal diabetes. © 2018
title Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes
title_short Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes
title_full Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes
title_fullStr Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes
title_full_unstemmed Altered FOXO1 activation in the programming of cardiovascular alterations by maternal diabetes
title_sort altered foxo1 activation in the programming of cardiovascular alterations by maternal diabetes
publishDate 2019
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03037207_v479_n_p78_Musikant
http://hdl.handle.net/20.500.12110/paper_03037207_v479_n_p78_Musikant
_version_ 1768545599991316480