Matches in SemOpenAlex for { <https://semopenalex.org/work/W2394501982> ?p ?o ?g. }
- W2394501982 endingPage "777" @default.
- W2394501982 startingPage "768" @default.
- W2394501982 abstract "New Findings What is the central question of this study? Endoplasmic reticulum (ER) stress has been reported to be involved in type 2 diabetes; however, the role of exacerbated ER stress in vascular dysfunction in type 2 diabetes remains unknown. What is the main finding and its importance? The main findings of this study are that ER stress is increased in the coronary arteries in type 2 diabetes, and inhibition of ER stress using taurine‐conjugated ursodeoxycholic acid improves vascular function, which is associated with normalization of the myogenic response and endothelium‐dependent relaxation. Vascular dysfunction is a major complication in type 2 diabetes. Although endoplasmic reticulum (ER) stress has been suggested to be a contributory factor in cardiovascular diseases, the relationship between ER stress and vascular dysfunction in type 2 diabetes remains unclear. Thus, in the present study, we examined whether ER stress contributes to coronary artery dysfunction and whether inhibition of ER stress ameliorates vascular function in type 2 diabetes. Type 2 diabetic mice and their control counterparts were treated with an ER stress inhibitor (taurine‐conjugated ursodeoxycholic acid, 150 mg kg −1 day −1 , by i.p . injection) for 2 weeks or not treated. The myogenic response and endothelium‐dependent relaxation were measured in pressurized coronary arteries. In type 2 diabetic mice, blood glucose and body weight were elevated compared with control mice. The myogenic response was potentiated and endothelium‐dependent relaxation impaired in coronary arteries from the type 2 diabetic mice. Interestingly, treatment with the ER stress inhibitor normalized the myogenic responses and endothelium‐dependent relaxation. These data were associated with an increase in ER stress marker expression or phosphorylation (IRE1‐XBP‐1 and PERK‐eIF2α) in type 2 diabetic mice, which were reduced by treatment with the ER stress inhibitor. Inhibition of ER stress normalizes the myogenic response and improves vascular function in type 2 diabetes. Therefore, ER stress could be a potential target for cardiovascular diseases in diabetes mellitus." @default.
- W2394501982 created "2016-06-24" @default.
- W2394501982 creator A5012483062 @default.
- W2394501982 creator A5024609610 @default.
- W2394501982 creator A5044132716 @default.
- W2394501982 creator A5063098085 @default.
- W2394501982 date "2016-05-01" @default.
- W2394501982 modified "2023-10-03" @default.
- W2394501982 title "Inhibition of endoplasmic reticulum stress improves coronary artery function in type 2 diabetic mice" @default.
- W2394501982 cites W1902029503 @default.
- W2394501982 cites W1955419087 @default.
- W2394501982 cites W1966207061 @default.
- W2394501982 cites W1966625828 @default.
- W2394501982 cites W1977603207 @default.
- W2394501982 cites W1982825238 @default.
- W2394501982 cites W2007078899 @default.
- W2394501982 cites W2007406273 @default.
- W2394501982 cites W2016326896 @default.
- W2394501982 cites W2042130085 @default.
- W2394501982 cites W2044437167 @default.
- W2394501982 cites W2048456744 @default.
- W2394501982 cites W2074549465 @default.
- W2394501982 cites W2079299190 @default.
- W2394501982 cites W2091595721 @default.
- W2394501982 cites W2097316277 @default.
- W2394501982 cites W2105624667 @default.
- W2394501982 cites W2115019805 @default.
- W2394501982 cites W2128810030 @default.
- W2394501982 cites W2130326770 @default.
- W2394501982 cites W2135279920 @default.
- W2394501982 cites W2153074213 @default.
- W2394501982 cites W2163481427 @default.
- W2394501982 cites W2170651004 @default.
- W2394501982 cites W2258583203 @default.
- W2394501982 cites W2337454357 @default.
- W2394501982 cites W2769264260 @default.
- W2394501982 cites W4250374989 @default.
- W2394501982 cites W787120501 @default.
- W2394501982 doi "https://doi.org/10.1113/ep085508" @default.
- W2394501982 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26990483" @default.
- W2394501982 hasPublicationYear "2016" @default.
- W2394501982 type Work @default.
- W2394501982 sameAs 2394501982 @default.
- W2394501982 citedByCount "32" @default.
- W2394501982 countsByYear W23945019822016 @default.
- W2394501982 countsByYear W23945019822017 @default.
- W2394501982 countsByYear W23945019822018 @default.
- W2394501982 countsByYear W23945019822019 @default.
- W2394501982 countsByYear W23945019822020 @default.
- W2394501982 countsByYear W23945019822021 @default.
- W2394501982 countsByYear W23945019822022 @default.
- W2394501982 countsByYear W23945019822023 @default.
- W2394501982 crossrefType "journal-article" @default.
- W2394501982 hasAuthorship W2394501982A5012483062 @default.
- W2394501982 hasAuthorship W2394501982A5024609610 @default.
- W2394501982 hasAuthorship W2394501982A5044132716 @default.
- W2394501982 hasAuthorship W2394501982A5063098085 @default.
- W2394501982 hasBestOaLocation W23945019821 @default.
- W2394501982 hasConcept C126322002 @default.
- W2394501982 hasConcept C134018914 @default.
- W2394501982 hasConcept C139447449 @default.
- W2394501982 hasConcept C158617107 @default.
- W2394501982 hasConcept C185592680 @default.
- W2394501982 hasConcept C2776820930 @default.
- W2394501982 hasConcept C2776992346 @default.
- W2394501982 hasConcept C2777180221 @default.
- W2394501982 hasConcept C2778742706 @default.
- W2394501982 hasConcept C2779395532 @default.
- W2394501982 hasConcept C2780972559 @default.
- W2394501982 hasConcept C2992686903 @default.
- W2394501982 hasConcept C55493867 @default.
- W2394501982 hasConcept C555293320 @default.
- W2394501982 hasConcept C71924100 @default.
- W2394501982 hasConceptScore W2394501982C126322002 @default.
- W2394501982 hasConceptScore W2394501982C134018914 @default.
- W2394501982 hasConceptScore W2394501982C139447449 @default.
- W2394501982 hasConceptScore W2394501982C158617107 @default.
- W2394501982 hasConceptScore W2394501982C185592680 @default.
- W2394501982 hasConceptScore W2394501982C2776820930 @default.
- W2394501982 hasConceptScore W2394501982C2776992346 @default.
- W2394501982 hasConceptScore W2394501982C2777180221 @default.
- W2394501982 hasConceptScore W2394501982C2778742706 @default.
- W2394501982 hasConceptScore W2394501982C2779395532 @default.
- W2394501982 hasConceptScore W2394501982C2780972559 @default.
- W2394501982 hasConceptScore W2394501982C2992686903 @default.
- W2394501982 hasConceptScore W2394501982C55493867 @default.
- W2394501982 hasConceptScore W2394501982C555293320 @default.
- W2394501982 hasConceptScore W2394501982C71924100 @default.
- W2394501982 hasIssue "6" @default.
- W2394501982 hasLocation W23945019821 @default.
- W2394501982 hasLocation W23945019822 @default.
- W2394501982 hasOpenAccess W2394501982 @default.
- W2394501982 hasPrimaryLocation W23945019821 @default.
- W2394501982 hasRelatedWork W134980868 @default.
- W2394501982 hasRelatedWork W2091193686 @default.
- W2394501982 hasRelatedWork W2122859970 @default.
- W2394501982 hasRelatedWork W2143238233 @default.
- W2394501982 hasRelatedWork W2534946788 @default.