Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery
Main Author: | |
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Publication Date: | 2021 |
Other Authors: | , , , , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.3389/fendo.2021.701994 http://hdl.handle.net/11449/231512 |
Summary: | Obesity and insulin resistance (IR) are well-studied risk factors for systemic cardiovascular disease, but their impact on pulmonary hypertension (PH) is not well clarified. This study aims to investigate if diet-induced obesity induces PH and if peroxisome-proliferator-activated receptor (PPAR-γ) and/or endoplasmic reticulum (ER) stress are involved in this process. Mice were maintained on a high-fat diet (HFD) for 4 months, and IR and PH were confirmed. In a separate group, after 4 months of HFD, mice were treated with pioglitazone (PIO) or 4-phenylbutyric acid for the last month. The results demonstrated that HFD for at least 4 months is able to increase pulmonary artery pressure, which is maintained, and this animal model can be used to investigate the link between IR and PH, without changes in ER stress in the pulmonary artery. There was also a reduction in circulating adiponectin and in perivascular adiponectin expression in the pulmonary artery, associated with a reduction in PPAR-γ expression. Treatment with PIO improved IR and PH and reversed the lower expression of adiponectin and PPAR-γ in the pulmonary artery, highlighting this drug as potential benefit for this poorly recognized complication of obesity. |
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Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Arteryhigh-fat (HF) dietinsulin resistanceobesitypioglitazonePPAR-γObesity and insulin resistance (IR) are well-studied risk factors for systemic cardiovascular disease, but their impact on pulmonary hypertension (PH) is not well clarified. This study aims to investigate if diet-induced obesity induces PH and if peroxisome-proliferator-activated receptor (PPAR-γ) and/or endoplasmic reticulum (ER) stress are involved in this process. Mice were maintained on a high-fat diet (HFD) for 4 months, and IR and PH were confirmed. In a separate group, after 4 months of HFD, mice were treated with pioglitazone (PIO) or 4-phenylbutyric acid for the last month. The results demonstrated that HFD for at least 4 months is able to increase pulmonary artery pressure, which is maintained, and this animal model can be used to investigate the link between IR and PH, without changes in ER stress in the pulmonary artery. There was also a reduction in circulating adiponectin and in perivascular adiponectin expression in the pulmonary artery, associated with a reduction in PPAR-γ expression. Treatment with PIO improved IR and PH and reversed the lower expression of adiponectin and PPAR-γ in the pulmonary artery, highlighting this drug as potential benefit for this poorly recognized complication of obesity.Department of Internal Medicine Faculty of Medicine State University of CampinasDepartment of Physical Education São Paulo State University (UNESP)Heart Institute (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São PauloDepartment of Physical Education São Paulo State University (UNESP)Universidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Gonçalves, Any Elisa de Souza SchmidtRocha, Guilherme ZweigMarin, RodrigoCamargo, Rafael LudemannSantos, Andrey dosCarmo, Helison doGuadagnini, DiozePetrucci, OrlandoMoysés, Zenaide ProvidelloSalemi, Vera Maria CuryOliveira, Alexandre Gabarra [UNESP]Saad, Mario José Abdalla2022-04-29T08:45:55Z2022-04-29T08:45:55Z2021-09-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3389/fendo.2021.701994Frontiers in Endocrinology, v. 12.1664-2392http://hdl.handle.net/11449/23151210.3389/fendo.2021.7019942-s2.0-85115231329Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFrontiers in Endocrinologyinfo:eu-repo/semantics/openAccess2024-09-30T17:35:42Zoai:repositorio.unesp.br:11449/231512Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-30T17:35:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
title |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
spellingShingle |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery Gonçalves, Any Elisa de Souza Schmidt high-fat (HF) diet insulin resistance obesity pioglitazone PPAR-γ |
title_short |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
title_full |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
title_fullStr |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
title_full_unstemmed |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
title_sort |
Pulmonary Hypertension in Obese Mice Is Accompanied by a Reduction in PPAR-γ Expression in Pulmonary Artery |
author |
Gonçalves, Any Elisa de Souza Schmidt |
author_facet |
Gonçalves, Any Elisa de Souza Schmidt Rocha, Guilherme Zweig Marin, Rodrigo Camargo, Rafael Ludemann Santos, Andrey dos Carmo, Helison do Guadagnini, Dioze Petrucci, Orlando Moysés, Zenaide Providello Salemi, Vera Maria Cury Oliveira, Alexandre Gabarra [UNESP] Saad, Mario José Abdalla |
author_role |
author |
author2 |
Rocha, Guilherme Zweig Marin, Rodrigo Camargo, Rafael Ludemann Santos, Andrey dos Carmo, Helison do Guadagnini, Dioze Petrucci, Orlando Moysés, Zenaide Providello Salemi, Vera Maria Cury Oliveira, Alexandre Gabarra [UNESP] Saad, Mario José Abdalla |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Campinas (UNICAMP) Universidade Estadual Paulista (UNESP) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Gonçalves, Any Elisa de Souza Schmidt Rocha, Guilherme Zweig Marin, Rodrigo Camargo, Rafael Ludemann Santos, Andrey dos Carmo, Helison do Guadagnini, Dioze Petrucci, Orlando Moysés, Zenaide Providello Salemi, Vera Maria Cury Oliveira, Alexandre Gabarra [UNESP] Saad, Mario José Abdalla |
dc.subject.por.fl_str_mv |
high-fat (HF) diet insulin resistance obesity pioglitazone PPAR-γ |
topic |
high-fat (HF) diet insulin resistance obesity pioglitazone PPAR-γ |
description |
Obesity and insulin resistance (IR) are well-studied risk factors for systemic cardiovascular disease, but their impact on pulmonary hypertension (PH) is not well clarified. This study aims to investigate if diet-induced obesity induces PH and if peroxisome-proliferator-activated receptor (PPAR-γ) and/or endoplasmic reticulum (ER) stress are involved in this process. Mice were maintained on a high-fat diet (HFD) for 4 months, and IR and PH were confirmed. In a separate group, after 4 months of HFD, mice were treated with pioglitazone (PIO) or 4-phenylbutyric acid for the last month. The results demonstrated that HFD for at least 4 months is able to increase pulmonary artery pressure, which is maintained, and this animal model can be used to investigate the link between IR and PH, without changes in ER stress in the pulmonary artery. There was also a reduction in circulating adiponectin and in perivascular adiponectin expression in the pulmonary artery, associated with a reduction in PPAR-γ expression. Treatment with PIO improved IR and PH and reversed the lower expression of adiponectin and PPAR-γ in the pulmonary artery, highlighting this drug as potential benefit for this poorly recognized complication of obesity. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-09-06 2022-04-29T08:45:55Z 2022-04-29T08:45:55Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3389/fendo.2021.701994 Frontiers in Endocrinology, v. 12. 1664-2392 http://hdl.handle.net/11449/231512 10.3389/fendo.2021.701994 2-s2.0-85115231329 |
url |
http://dx.doi.org/10.3389/fendo.2021.701994 http://hdl.handle.net/11449/231512 |
identifier_str_mv |
Frontiers in Endocrinology, v. 12. 1664-2392 10.3389/fendo.2021.701994 2-s2.0-85115231329 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Frontiers in Endocrinology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1834483835566292992 |