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Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation

Prenatal alcohol exposure (PAE) impairs fetal development. Alcohol consumption was shown to modulate the renin–angiotensin system (RAS). This study aimed to analyze the effects of PAE on the expression of the renin–angiotensin system (RAS) and kallikrein–kinin system (KKS) peptide systems in the hip...

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Autores principales: da Silva, Gabriel Almeida, Atum, Allan Luís Barboza, de Matos, Leonardo Paroche, Nasuk, Guilherme Rabelo, de Jesus, Bruna Calixto, Gouveia, Telma Luciana Furtado, Baltatu, Ovidiu Constantin, Zamuner, Stella Regina, Silva Júnior, José Antônio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045732/
https://www.ncbi.nlm.nih.gov/pubmed/36978790
http://dx.doi.org/10.3390/antiox12030541
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author da Silva, Gabriel Almeida
Atum, Allan Luís Barboza
de Matos, Leonardo Paroche
Nasuk, Guilherme Rabelo
de Jesus, Bruna Calixto
Gouveia, Telma Luciana Furtado
Baltatu, Ovidiu Constantin
Zamuner, Stella Regina
Silva Júnior, José Antônio
author_facet da Silva, Gabriel Almeida
Atum, Allan Luís Barboza
de Matos, Leonardo Paroche
Nasuk, Guilherme Rabelo
de Jesus, Bruna Calixto
Gouveia, Telma Luciana Furtado
Baltatu, Ovidiu Constantin
Zamuner, Stella Regina
Silva Júnior, José Antônio
author_sort da Silva, Gabriel Almeida
collection PubMed
description Prenatal alcohol exposure (PAE) impairs fetal development. Alcohol consumption was shown to modulate the renin–angiotensin system (RAS). This study aimed to analyze the effects of PAE on the expression of the renin–angiotensin system (RAS) and kallikrein–kinin system (KKS) peptide systems in the hippocampus and heart of mice of both sexes. C57Bl/6 mice were exposed to alcohol during pregnancy at a concentration of 10% (v/v). On postnatal day 45 (PN45), mouse hippocampi and left ventricles (LV) were collected and processed for messenger RNA (mRNA) expression of components of the RAS and KKS. In PAE animals, more pronounced expression of AT1 and ACE mRNAs in males and a restored AT2 mRNA expression in females were observed in both tissues. In LV, increased AT2, ACE2, and B2 mRNA expressions were also observed in PAE females. Furthermore, high levels of H(2)O(2) were observed in males from the PAE group in both tissues. Taken together, our results suggest that modulation of the expression of these peptidergic systems in PAE females may make them less susceptible to the effects of alcohol.
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spelling pubmed-100457322023-03-29 Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation da Silva, Gabriel Almeida Atum, Allan Luís Barboza de Matos, Leonardo Paroche Nasuk, Guilherme Rabelo de Jesus, Bruna Calixto Gouveia, Telma Luciana Furtado Baltatu, Ovidiu Constantin Zamuner, Stella Regina Silva Júnior, José Antônio Antioxidants (Basel) Article Prenatal alcohol exposure (PAE) impairs fetal development. Alcohol consumption was shown to modulate the renin–angiotensin system (RAS). This study aimed to analyze the effects of PAE on the expression of the renin–angiotensin system (RAS) and kallikrein–kinin system (KKS) peptide systems in the hippocampus and heart of mice of both sexes. C57Bl/6 mice were exposed to alcohol during pregnancy at a concentration of 10% (v/v). On postnatal day 45 (PN45), mouse hippocampi and left ventricles (LV) were collected and processed for messenger RNA (mRNA) expression of components of the RAS and KKS. In PAE animals, more pronounced expression of AT1 and ACE mRNAs in males and a restored AT2 mRNA expression in females were observed in both tissues. In LV, increased AT2, ACE2, and B2 mRNA expressions were also observed in PAE females. Furthermore, high levels of H(2)O(2) were observed in males from the PAE group in both tissues. Taken together, our results suggest that modulation of the expression of these peptidergic systems in PAE females may make them less susceptible to the effects of alcohol. MDPI 2023-02-21 /pmc/articles/PMC10045732/ /pubmed/36978790 http://dx.doi.org/10.3390/antiox12030541 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
da Silva, Gabriel Almeida
Atum, Allan Luís Barboza
de Matos, Leonardo Paroche
Nasuk, Guilherme Rabelo
de Jesus, Bruna Calixto
Gouveia, Telma Luciana Furtado
Baltatu, Ovidiu Constantin
Zamuner, Stella Regina
Silva Júnior, José Antônio
Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation
title Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation
title_full Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation
title_fullStr Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation
title_full_unstemmed Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation
title_short Sexual Dimorphism in the Expression of Cardiac and Hippocampal Renin-Angiotensin and Kallikrein–Kinin Systems in Offspring from Mice Exposed to Alcohol during Gestation
title_sort sexual dimorphism in the expression of cardiac and hippocampal renin-angiotensin and kallikrein–kinin systems in offspring from mice exposed to alcohol during gestation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045732/
https://www.ncbi.nlm.nih.gov/pubmed/36978790
http://dx.doi.org/10.3390/antiox12030541
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