Matches in SemOpenAlex for { <https://semopenalex.org/work/W4384492887> ?p ?o ?g. }
- W4384492887 abstract "Background Estrogen Receptor α (ERα) is a significant modulator of energy balance and lipid/glucose metabolisms. Beyond the classical nuclear actions of the receptor, rapid activation of intracellular signaling pathways is mediated by a sub-fraction of ERα localized to the plasma membrane, known as Membrane Initiated Steroid Signaling (MISS). However, whether membrane ERα is involved in the protective metabolic actions of endogenous estrogens in conditions of nutritional challenge, and thus contributes to sex differences in the susceptibility to metabolic diseases, remains to be clarified. Methods Male and female C451A-ERα mice, harboring a point mutation which results in the abolition of membrane localization and MISS-related effects of the receptor, and their wild-type littermates ( WT-ERα ) were maintained on a normal chow diet (NCD) or fed a high-fat diet (HFD). Body weight gain, body composition and glucose tolerance were monitored. Insulin sensitivity and energy balance regulation were further investigated in HFD-fed female mice. Results C451A-ERα genotype had no influence on body weight gain, adipose tissue accumulation and glucose tolerance in NCD-fed mice of both sexes followed up to 7 months of age, nor male mice fed a HFD for 12 weeks. In contrast, compared to WT-ERα littermates, HFD-fed C451A-ERα female mice exhibited: 1) accelerated fat mass accumulation, liver steatosis and impaired glucose tolerance; 2) whole-body insulin resistance, assessed by hyperinsulinemic-euglycemic clamps, and altered insulin-induced signaling in skeletal muscle and liver; 3) significant decrease in energy expenditure associated with histological and functional abnormalities of brown adipose tissue and a defect in thermogenesis regulation in response to cold exposure. Conclusion Besides the well-characterized role of ERα nuclear actions, membrane-initiated ERα extra-nuclear signaling contributes to female, but not to male, protection against HFD-induced obesity and associated metabolic disorders in mouse." @default.
- W4384492887 created "2023-07-18" @default.
- W4384492887 creator A5000940573 @default.
- W4384492887 creator A5026393485 @default.
- W4384492887 creator A5035525241 @default.
- W4384492887 creator A5037101201 @default.
- W4384492887 creator A5039930068 @default.
- W4384492887 creator A5043815002 @default.
- W4384492887 creator A5047653403 @default.
- W4384492887 creator A5050750512 @default.
- W4384492887 creator A5059232587 @default.
- W4384492887 creator A5065824018 @default.
- W4384492887 creator A5074147890 @default.
- W4384492887 creator A5076363167 @default.
- W4384492887 date "2023-07-17" @default.
- W4384492887 modified "2023-10-14" @default.
- W4384492887 title "Membrane estrogen receptor-α contributes to female protection against high-fat diet-induced metabolic disorders" @default.
- W4384492887 cites W1976257390 @default.
- W4384492887 cites W1978262912 @default.
- W4384492887 cites W2007975243 @default.
- W4384492887 cites W2013865699 @default.
- W4384492887 cites W2035785296 @default.
- W4384492887 cites W2037621705 @default.
- W4384492887 cites W2043659942 @default.
- W4384492887 cites W2046082610 @default.
- W4384492887 cites W2066332959 @default.
- W4384492887 cites W2113576333 @default.
- W4384492887 cites W2123432388 @default.
- W4384492887 cites W2124375064 @default.
- W4384492887 cites W2132261361 @default.
- W4384492887 cites W2148956334 @default.
- W4384492887 cites W2151390490 @default.
- W4384492887 cites W2155658630 @default.
- W4384492887 cites W2156831368 @default.
- W4384492887 cites W2166524464 @default.
- W4384492887 cites W2227807199 @default.
- W4384492887 cites W2321613759 @default.
- W4384492887 cites W2404874301 @default.
- W4384492887 cites W2475250396 @default.
- W4384492887 cites W2507771110 @default.
- W4384492887 cites W2595844509 @default.
- W4384492887 cites W2618142594 @default.
- W4384492887 cites W2791711670 @default.
- W4384492887 cites W2803267200 @default.
- W4384492887 cites W2804262814 @default.
- W4384492887 cites W2808538861 @default.
- W4384492887 cites W2810116258 @default.
- W4384492887 cites W2891835591 @default.
- W4384492887 cites W2897315531 @default.
- W4384492887 cites W2991033511 @default.
- W4384492887 cites W3045019283 @default.
- W4384492887 cites W3047361803 @default.
- W4384492887 cites W3089051780 @default.
- W4384492887 cites W3201264063 @default.
- W4384492887 cites W3203947777 @default.
- W4384492887 cites W3213926446 @default.
- W4384492887 doi "https://doi.org/10.3389/fendo.2023.1215947" @default.
- W4384492887 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37529599" @default.
- W4384492887 hasPublicationYear "2023" @default.
- W4384492887 type Work @default.
- W4384492887 citedByCount "0" @default.
- W4384492887 crossrefType "journal-article" @default.
- W4384492887 hasAuthorship W4384492887A5000940573 @default.
- W4384492887 hasAuthorship W4384492887A5026393485 @default.
- W4384492887 hasAuthorship W4384492887A5035525241 @default.
- W4384492887 hasAuthorship W4384492887A5037101201 @default.
- W4384492887 hasAuthorship W4384492887A5039930068 @default.
- W4384492887 hasAuthorship W4384492887A5043815002 @default.
- W4384492887 hasAuthorship W4384492887A5047653403 @default.
- W4384492887 hasAuthorship W4384492887A5050750512 @default.
- W4384492887 hasAuthorship W4384492887A5059232587 @default.
- W4384492887 hasAuthorship W4384492887A5065824018 @default.
- W4384492887 hasAuthorship W4384492887A5074147890 @default.
- W4384492887 hasAuthorship W4384492887A5076363167 @default.
- W4384492887 hasBestOaLocation W43844928871 @default.
- W4384492887 hasConcept C112446052 @default.
- W4384492887 hasConcept C121608353 @default.
- W4384492887 hasConcept C126322002 @default.
- W4384492887 hasConcept C134018914 @default.
- W4384492887 hasConcept C151955695 @default.
- W4384492887 hasConcept C171089720 @default.
- W4384492887 hasConcept C2776175330 @default.
- W4384492887 hasConcept C2777164284 @default.
- W4384492887 hasConcept C2777180221 @default.
- W4384492887 hasConcept C2777391703 @default.
- W4384492887 hasConcept C2778772119 @default.
- W4384492887 hasConcept C2779134260 @default.
- W4384492887 hasConcept C2779306644 @default.
- W4384492887 hasConcept C2780609358 @default.
- W4384492887 hasConcept C530470458 @default.
- W4384492887 hasConcept C555293320 @default.
- W4384492887 hasConcept C71924100 @default.
- W4384492887 hasConcept C84606932 @default.
- W4384492887 hasConcept C86803240 @default.
- W4384492887 hasConceptScore W4384492887C112446052 @default.
- W4384492887 hasConceptScore W4384492887C121608353 @default.
- W4384492887 hasConceptScore W4384492887C126322002 @default.
- W4384492887 hasConceptScore W4384492887C134018914 @default.
- W4384492887 hasConceptScore W4384492887C151955695 @default.
- W4384492887 hasConceptScore W4384492887C171089720 @default.