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Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model

Overconsumption of fructose leads to metabolic syndrome as a result of hypertension, insulin resistance, and hyperlipidemia. In this study, the renal function of animals submitted to high fructose intake was analyzed from weaning to adulthood using in vivo and ex vivo methods, being compared with a...

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Autores principales: Yokota, Rodrigo, Ronchi, Fernanda Aparecida, Fernandes, Fernanda Barrinha, Jara, Zaira Palomino, Rosa, Rodolfo Mattar, Leite, Ana Paula de Oliveira, Fiorino, Patricia, Farah, Vera, do Nascimento, Nilberto Robson Falcão, Fonteles, Manassés C., Casarini, Dulce Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191567/
https://www.ncbi.nlm.nih.gov/pubmed/30364140
http://dx.doi.org/10.3389/fphys.2018.01433
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author Yokota, Rodrigo
Ronchi, Fernanda Aparecida
Fernandes, Fernanda Barrinha
Jara, Zaira Palomino
Rosa, Rodolfo Mattar
Leite, Ana Paula de Oliveira
Fiorino, Patricia
Farah, Vera
do Nascimento, Nilberto Robson Falcão
Fonteles, Manassés C.
Casarini, Dulce Elena
author_facet Yokota, Rodrigo
Ronchi, Fernanda Aparecida
Fernandes, Fernanda Barrinha
Jara, Zaira Palomino
Rosa, Rodolfo Mattar
Leite, Ana Paula de Oliveira
Fiorino, Patricia
Farah, Vera
do Nascimento, Nilberto Robson Falcão
Fonteles, Manassés C.
Casarini, Dulce Elena
author_sort Yokota, Rodrigo
collection PubMed
description Overconsumption of fructose leads to metabolic syndrome as a result of hypertension, insulin resistance, and hyperlipidemia. In this study, the renal function of animals submitted to high fructose intake was analyzed from weaning to adulthood using in vivo and ex vivo methods, being compared with a normal control group. We investigated in ex vivo model of the role of the renin Angiotensin system (RAS) in the kidney. The use of perfused kidney from animals submitted to 8-week fructose treatment showed that high fructose intake caused metabolic and cardiovascular alterations that were consistent with other studies. Moreover, the isolated perfused kidneys obtained from rats under high fructose diet showed a 33% increase in renal perfusion pressure throughout the experimental period due to increased renal vascular resistance and a progressive fall in the glomerular filtration rate, which reached a maximum of 64% decrease. Analysis of RAS peptides in the high fructose group showed a threefold increase in the renal concentrations of angiotensin I (Ang I) and a twofold increase in angiotensin II (Ang II) levels, whereas no change in angiotensin 1-7 (Ang 1-7) was observed when compared with the control animals. We did not detect changes in angiotensin converting enzyme (ACE) activity in renal tissues, but there is a tendency to decrease. These observations suggest that there are alternative ways of producing Ang II in this model. Chymase the enzyme responsible for Ang II formation direct from Ang I was increased in renal tissues in the fructose group, confirming the alternative pathway for the formation of this peptide. Neprilysin (NEP) the Ang 1-7 forming showed a significant decrease in activity in the fructose vs. control group, and a tendency of reduction in ACE2 activity. Thus, these results suggest that the Ang 1-7 vasodilator peptide formation is impaired in this model contributing with the increase of blood pressure. In summary, rats fed high fructose affect renal RAS, which may contribute to several deleterious effects of fructose on the kidneys and consequently an increase in blood pressure.
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spelling pubmed-61915672018-10-24 Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model Yokota, Rodrigo Ronchi, Fernanda Aparecida Fernandes, Fernanda Barrinha Jara, Zaira Palomino Rosa, Rodolfo Mattar Leite, Ana Paula de Oliveira Fiorino, Patricia Farah, Vera do Nascimento, Nilberto Robson Falcão Fonteles, Manassés C. Casarini, Dulce Elena Front Physiol Physiology Overconsumption of fructose leads to metabolic syndrome as a result of hypertension, insulin resistance, and hyperlipidemia. In this study, the renal function of animals submitted to high fructose intake was analyzed from weaning to adulthood using in vivo and ex vivo methods, being compared with a normal control group. We investigated in ex vivo model of the role of the renin Angiotensin system (RAS) in the kidney. The use of perfused kidney from animals submitted to 8-week fructose treatment showed that high fructose intake caused metabolic and cardiovascular alterations that were consistent with other studies. Moreover, the isolated perfused kidneys obtained from rats under high fructose diet showed a 33% increase in renal perfusion pressure throughout the experimental period due to increased renal vascular resistance and a progressive fall in the glomerular filtration rate, which reached a maximum of 64% decrease. Analysis of RAS peptides in the high fructose group showed a threefold increase in the renal concentrations of angiotensin I (Ang I) and a twofold increase in angiotensin II (Ang II) levels, whereas no change in angiotensin 1-7 (Ang 1-7) was observed when compared with the control animals. We did not detect changes in angiotensin converting enzyme (ACE) activity in renal tissues, but there is a tendency to decrease. These observations suggest that there are alternative ways of producing Ang II in this model. Chymase the enzyme responsible for Ang II formation direct from Ang I was increased in renal tissues in the fructose group, confirming the alternative pathway for the formation of this peptide. Neprilysin (NEP) the Ang 1-7 forming showed a significant decrease in activity in the fructose vs. control group, and a tendency of reduction in ACE2 activity. Thus, these results suggest that the Ang 1-7 vasodilator peptide formation is impaired in this model contributing with the increase of blood pressure. In summary, rats fed high fructose affect renal RAS, which may contribute to several deleterious effects of fructose on the kidneys and consequently an increase in blood pressure. Frontiers Media S.A. 2018-10-10 /pmc/articles/PMC6191567/ /pubmed/30364140 http://dx.doi.org/10.3389/fphys.2018.01433 Text en Copyright © 2018 Yokota, Ronchi, Fernandes, Jara, Rosa, Leite, Fiorino, Farah, Nascimento, Fonteles and Casarini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Yokota, Rodrigo
Ronchi, Fernanda Aparecida
Fernandes, Fernanda Barrinha
Jara, Zaira Palomino
Rosa, Rodolfo Mattar
Leite, Ana Paula de Oliveira
Fiorino, Patricia
Farah, Vera
do Nascimento, Nilberto Robson Falcão
Fonteles, Manassés C.
Casarini, Dulce Elena
Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model
title Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model
title_full Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model
title_fullStr Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model
title_full_unstemmed Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model
title_short Intra-Renal Angiotensin Levels Are Increased in High-Fructose Fed Rats in the Extracorporeal Renal Perfusion Model
title_sort intra-renal angiotensin levels are increased in high-fructose fed rats in the extracorporeal renal perfusion model
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191567/
https://www.ncbi.nlm.nih.gov/pubmed/30364140
http://dx.doi.org/10.3389/fphys.2018.01433
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