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1000 Titel
  • Cortical multisensory integration—a special role of the agranular insular cortex?
1000 Autor/in
  1. Brunert, Daniela |
  2. Rothermel, Markus |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-05-26
1000 Erschienen in
1000 Quellenangabe
  • 472(6):671-672
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00424-020-02400-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293668/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Sirtuin1 deficiency or reduced activity comprises one of the hallmarks of diseases as diverse as chronic cardiovascular, renal, and metabolic, some malignancies, and infections, as well as aging-associated diseases. In a mouse model of endothelium-limited defect in sirtuin 1 deacetylase activity, we found a dramatic reduction in the volume of endothelial glycocalyx. This was associated with the surge in the levels of one of key scaffolding heparan sulfate proteoglycans of endothelial glycocalyx, syndecan-4, and specifically, its extracellular domain (ectodomain). We found that the defect in endothelial sirtuin 1 deacetylase activity is associated with (a) elevated basal and stimulated levels of superoxide generation (via the FoxO1 over-acetylation mechanism) and (b) increased nuclear translocation of NF-kB (via p65 over-acetylation mechanism). These findings laid the foundation for the proposed novel function of sirtuin 1, namely, the maintenance of endothelial glycocalyx, particularly manifest in conditions associated with sirtuin 1 depletion. In the forthcoming review, we summarize the emerging conceptual framework of the enhanced glycocalyx degradation in the states of defective endothelial sirtuin 1 function, thus explaining a broad footprint of the syndrome of endothelial dysfunction, from impaired flow-induced nitric oxide production, deterrent leukocytes infiltration, increased endothelial permeability, coagulation, and pro-inflammatory changes to development of microvascular rarefaction and progression of an underlying disease.
1000 Sacherschließung
lokal Thalamus [MeSH]
lokal Cerebral Cortex [MeSH]
lokal Chorda Tympani Nerve [MeSH]
lokal Human Physiology
lokal Rats [MeSH]
lokal Molecular Medicine
lokal Taste [MeSH]
lokal Commentary
lokal Cell Biology
lokal Animals [MeSH]
lokal Receptors
lokal Olfactory Bulb [MeSH]
lokal Neurosciences
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/QnJ1bmVydCwgRGFuaWVsYQ==|https://orcid.org/0000-0002-0929-993X
1000 Hinweis
  • DeepGreen-ID: e10cc9e0f4ed4356844900a3f80cf77c ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 @id frl:6467272.rdf
1000 Erstellt am 2023-11-17T09:01:33.592+0100
1000 Erstellt von 322
1000 beschreibt frl:6467272
1000 Zuletzt bearbeitet Fri Dec 01 05:57:27 CET 2023
1000 Objekt bearb. Fri Dec 01 05:57:27 CET 2023
1000 Vgl. frl:6467272
1000 Oai Id
  1. oai:frl.publisso.de:frl:6467272 |
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