Cargando…

SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness

Excessive epithelial sodium channel activation in endothelium (EnNaC) increase oxidative stress and inflammation with associated cardiovascular abnormalities. Our recent data has shown that activation of EnNaC mediates aortic endoplasmic reticulum stress, redox oxidative stress, expression of pro-in...

Descripción completa

Detalles Bibliográficos
Autores principales: Jia, Guanghong, Habibi, Javad, Aroor, Annayya, Yang, Yan, Lastra, Guido, Hill, Michael, Whaley-Connell, Adam, Jaisser, Frederic, Sowers, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552327/
http://dx.doi.org/10.1210/js.2019-SAT-LB011
_version_ 1783424577609662464
author Jia, Guanghong
Habibi, Javad
Aroor, Annayya
Yang, Yan
Lastra, Guido
Hill, Michael
Whaley-Connell, Adam
Jaisser, Frederic
Sowers, James
author_facet Jia, Guanghong
Habibi, Javad
Aroor, Annayya
Yang, Yan
Lastra, Guido
Hill, Michael
Whaley-Connell, Adam
Jaisser, Frederic
Sowers, James
author_sort Jia, Guanghong
collection PubMed
description Excessive epithelial sodium channel activation in endothelium (EnNaC) increase oxidative stress and inflammation with associated cardiovascular abnormalities. Our recent data has shown that activation of EnNaC mediates aortic endoplasmic reticulum stress, redox oxidative stress, expression of pro-inflammatory cytokines, and aortic remodeling. These abnormalities are potentially related to abnormal expression and activation of sirtuin 1 (Sirt1) and AMP-activated protein kinase (AMPK) in metabolic disorders such as obesity. We hypothesized that EnNaC mediates Western diet (WD)-induced endothelium and aortic stiffness by increasing aortic oxidative stress and associated oxidative stress related inhibition of Sirt1 and AMPK expression and activation. Accordingly, sixteen to twenty week-old EnNaC(-/-) and wild type littermate female mice were fed a mouse chow or an obesogenic WD containing excess fat (46%) and fructose (17.5%) for 16 weeks. EnNaC activation mediated WD-induced increase of Na(+) currents in isolated lung endothelial cells, reduction of phosphorylation of endothelial nitric oxide synthase (eNOS), as well as impairment of aortic endothelium-dependent relaxation to acetylcholine (10(-9)-10(-4) mol/L) in a wire myograph. The expression and activation of Sirt1 and AMPK were inhibited in WD EnNaC(+/+) mice and these abnormalities were prevented in EnNaC(-/-) mice. Importantly, EnNaC specific KO prevented WD induced aortic oxidative stress and related endothelium stiffness and impairment of endothelium (NO)-dependent relaxation. These data suggest that endothelial specific EnNaC activation mediates WD-induced aortic oxidative stress, decreased expression and activation of Sirt1, AMPK, eNOS, as well as endothelial and aortic vessel stiffness. Unless otherwise noted, all abstracts presented at ENDO are embargoed until the date and time of presentation. For oral presentations, the abstracts are embargoed until the session begins. Abstracts presented at a news conference are embargoed until the date and time of the news conference. The Endocrine Society reserves the right to lift the embargo on specific abstracts that are selected for promotion prior to or during ENDO.
format Online
Article
Text
id pubmed-6552327
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Endocrine Society
record_format MEDLINE/PubMed
spelling pubmed-65523272019-06-13 SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness Jia, Guanghong Habibi, Javad Aroor, Annayya Yang, Yan Lastra, Guido Hill, Michael Whaley-Connell, Adam Jaisser, Frederic Sowers, James J Endocr Soc Cardiovascular Endocrinology Excessive epithelial sodium channel activation in endothelium (EnNaC) increase oxidative stress and inflammation with associated cardiovascular abnormalities. Our recent data has shown that activation of EnNaC mediates aortic endoplasmic reticulum stress, redox oxidative stress, expression of pro-inflammatory cytokines, and aortic remodeling. These abnormalities are potentially related to abnormal expression and activation of sirtuin 1 (Sirt1) and AMP-activated protein kinase (AMPK) in metabolic disorders such as obesity. We hypothesized that EnNaC mediates Western diet (WD)-induced endothelium and aortic stiffness by increasing aortic oxidative stress and associated oxidative stress related inhibition of Sirt1 and AMPK expression and activation. Accordingly, sixteen to twenty week-old EnNaC(-/-) and wild type littermate female mice were fed a mouse chow or an obesogenic WD containing excess fat (46%) and fructose (17.5%) for 16 weeks. EnNaC activation mediated WD-induced increase of Na(+) currents in isolated lung endothelial cells, reduction of phosphorylation of endothelial nitric oxide synthase (eNOS), as well as impairment of aortic endothelium-dependent relaxation to acetylcholine (10(-9)-10(-4) mol/L) in a wire myograph. The expression and activation of Sirt1 and AMPK were inhibited in WD EnNaC(+/+) mice and these abnormalities were prevented in EnNaC(-/-) mice. Importantly, EnNaC specific KO prevented WD induced aortic oxidative stress and related endothelium stiffness and impairment of endothelium (NO)-dependent relaxation. These data suggest that endothelial specific EnNaC activation mediates WD-induced aortic oxidative stress, decreased expression and activation of Sirt1, AMPK, eNOS, as well as endothelial and aortic vessel stiffness. Unless otherwise noted, all abstracts presented at ENDO are embargoed until the date and time of presentation. For oral presentations, the abstracts are embargoed until the session begins. Abstracts presented at a news conference are embargoed until the date and time of the news conference. The Endocrine Society reserves the right to lift the embargo on specific abstracts that are selected for promotion prior to or during ENDO. Endocrine Society 2019-04-30 /pmc/articles/PMC6552327/ http://dx.doi.org/10.1210/js.2019-SAT-LB011 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Cardiovascular Endocrinology
Jia, Guanghong
Habibi, Javad
Aroor, Annayya
Yang, Yan
Lastra, Guido
Hill, Michael
Whaley-Connell, Adam
Jaisser, Frederic
Sowers, James
SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness
title SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness
title_full SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness
title_fullStr SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness
title_full_unstemmed SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness
title_short SAT-LB011 Role of Endothelium Epithelial Sodium Channel in Arterial Stiffness
title_sort sat-lb011 role of endothelium epithelial sodium channel in arterial stiffness
topic Cardiovascular Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552327/
http://dx.doi.org/10.1210/js.2019-SAT-LB011
work_keys_str_mv AT jiaguanghong satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT habibijavad satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT aroorannayya satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT yangyan satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT lastraguido satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT hillmichael satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT whaleyconnelladam satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT jaisserfrederic satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness
AT sowersjames satlb011roleofendotheliumepithelialsodiumchannelinarterialstiffness