Matches in SemOpenAlex for { <https://semopenalex.org/work/W2287087675> ?p ?o ?g. }
- W2287087675 endingPage "943" @default.
- W2287087675 startingPage "935" @default.
- W2287087675 abstract "Rationale: Enhanced activation of the mineralocorticoid receptors (MRs) in cardiovascular tissues increases oxidative stress, maladaptive immune responses, and inflammation with associated functional vascular abnormalities. We previously demonstrated that consumption of a Western diet (WD) for 16 weeks results in aortic stiffening, and that these abnormalities were prevented by systemic MR blockade in female mice. However, the cell-specific role of endothelial cell MR (ECMR) in these maladaptive vascular effects has not been explored. Objective: We hypothesized that specific deletion of the ECMR would prevent WD-induced increases in endothelial sodium channel activation, reductions in bioavailable nitric oxide, increased vascular remodeling, and associated increases in vascular stiffness in females. Methods and Results: Four-week-old female ECMR knockout and wild-type mice were fed either mouse chow or WD for 16 weeks. WD feeding resulted in aortic stiffness and endothelial dysfunction as determined in vivo by pulse wave velocity and ex vivo by atomic force microscopy, and wire and pressure myography. The WD-induced aortic stiffness was associated with enhanced endothelial sodium channel activation, attenuated endothelial nitric oxide synthase activation, increased oxidative stress, a proinflammatory immune response and fibrosis. Conversely, cell-specific ECMR deficiency prevented WD-induced aortic fibrosis and stiffness in conjunction with reductions in endothelial sodium channel activation, oxidative stress and macrophage proinflammatory polarization, restoration of endothelial nitric oxide synthase activation. Conclusions: Increased ECMR signaling associated with consumption of a WD plays a key role in endothelial sodium channel activation, reduced nitric oxide production, oxidative stress, and inflammation that lead to aortic remodeling and stiffness in female mice." @default.
- W2287087675 created "2016-06-24" @default.
- W2287087675 creator A5001968810 @default.
- W2287087675 creator A5006171109 @default.
- W2287087675 creator A5008853362 @default.
- W2287087675 creator A5015102832 @default.
- W2287087675 creator A5018617193 @default.
- W2287087675 creator A5023043755 @default.
- W2287087675 creator A5036556067 @default.
- W2287087675 creator A5058451510 @default.
- W2287087675 creator A5061642960 @default.
- W2287087675 creator A5071689177 @default.
- W2287087675 creator A5072771199 @default.
- W2287087675 creator A5084918480 @default.
- W2287087675 date "2016-03-18" @default.
- W2287087675 modified "2023-10-06" @default.
- W2287087675 title "Endothelial Mineralocorticoid Receptor Mediates Diet-Induced Aortic Stiffness in Females" @default.
- W2287087675 cites W1516421005 @default.
- W2287087675 cites W1872613035 @default.
- W2287087675 cites W1951373717 @default.
- W2287087675 cites W1968493141 @default.
- W2287087675 cites W1969365096 @default.
- W2287087675 cites W1980115422 @default.
- W2287087675 cites W1985402074 @default.
- W2287087675 cites W1992653475 @default.
- W2287087675 cites W1994591006 @default.
- W2287087675 cites W1998795233 @default.
- W2287087675 cites W2004705341 @default.
- W2287087675 cites W2005240397 @default.
- W2287087675 cites W2009173742 @default.
- W2287087675 cites W2009681150 @default.
- W2287087675 cites W2012240256 @default.
- W2287087675 cites W2012416246 @default.
- W2287087675 cites W2027390553 @default.
- W2287087675 cites W2032144770 @default.
- W2287087675 cites W2037446200 @default.
- W2287087675 cites W2042196243 @default.
- W2287087675 cites W2042972403 @default.
- W2287087675 cites W2049270217 @default.
- W2287087675 cites W2058838648 @default.
- W2287087675 cites W2075394493 @default.
- W2287087675 cites W2088174143 @default.
- W2287087675 cites W2088660937 @default.
- W2287087675 cites W2093057757 @default.
- W2287087675 cites W2093209897 @default.
- W2287087675 cites W2093249614 @default.
- W2287087675 cites W2105082749 @default.
- W2287087675 cites W2106052381 @default.
- W2287087675 cites W2109723161 @default.
- W2287087675 cites W2113910051 @default.
- W2287087675 cites W2117451333 @default.
- W2287087675 cites W2120662805 @default.
- W2287087675 cites W2131207264 @default.
- W2287087675 cites W2133279051 @default.
- W2287087675 cites W2134567651 @default.
- W2287087675 cites W2148035278 @default.
- W2287087675 cites W2150024906 @default.
- W2287087675 cites W2150790437 @default.
- W2287087675 cites W2159401680 @default.
- W2287087675 cites W2161841978 @default.
- W2287087675 cites W2162908883 @default.
- W2287087675 cites W2163028543 @default.
- W2287087675 cites W2165792408 @default.
- W2287087675 cites W2168059813 @default.
- W2287087675 cites W2170851950 @default.
- W2287087675 cites W2173970962 @default.
- W2287087675 cites W2529491169 @default.
- W2287087675 doi "https://doi.org/10.1161/circresaha.115.308269" @default.
- W2287087675 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4798906" @default.
- W2287087675 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26879229" @default.
- W2287087675 hasPublicationYear "2016" @default.
- W2287087675 type Work @default.
- W2287087675 sameAs 2287087675 @default.
- W2287087675 citedByCount "133" @default.
- W2287087675 countsByYear W22870876752016 @default.
- W2287087675 countsByYear W22870876752017 @default.
- W2287087675 countsByYear W22870876752018 @default.
- W2287087675 countsByYear W22870876752019 @default.
- W2287087675 countsByYear W22870876752020 @default.
- W2287087675 countsByYear W22870876752021 @default.
- W2287087675 countsByYear W22870876752022 @default.
- W2287087675 countsByYear W22870876752023 @default.
- W2287087675 crossrefType "journal-article" @default.
- W2287087675 hasAuthorship W2287087675A5001968810 @default.
- W2287087675 hasAuthorship W2287087675A5006171109 @default.
- W2287087675 hasAuthorship W2287087675A5008853362 @default.
- W2287087675 hasAuthorship W2287087675A5015102832 @default.
- W2287087675 hasAuthorship W2287087675A5018617193 @default.
- W2287087675 hasAuthorship W2287087675A5023043755 @default.
- W2287087675 hasAuthorship W2287087675A5036556067 @default.
- W2287087675 hasAuthorship W2287087675A5058451510 @default.
- W2287087675 hasAuthorship W2287087675A5061642960 @default.
- W2287087675 hasAuthorship W2287087675A5071689177 @default.
- W2287087675 hasAuthorship W2287087675A5072771199 @default.
- W2287087675 hasAuthorship W2287087675A5084918480 @default.
- W2287087675 hasBestOaLocation W22870876752 @default.
- W2287087675 hasConcept C123012128 @default.
- W2287087675 hasConcept C126322002 @default.