SIRT1-dependent deacetylation of Txnip H3K9ac is critical for exenatide-improved diabetic kidney disease.
Diabetic kidney disease
Exenatide
Kidney-specific Sirt1 knockout
Txnip
Journal
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
received:
03
08
2023
revised:
11
09
2023
accepted:
12
09
2023
pubmed:
25
9
2023
medline:
25
9
2023
entrez:
24
9
2023
Statut:
ppublish
Résumé
Glucagon-like peptide 1 receptor agonist exenatide (exendin-4) has potential protective capabilities against diabetic kidney disease (DKD). However, the underlying mechanism has not been fully elucidated. The expression of thioredoxin-interacting protein (Txnip) is upregulated during DKD progression by histone acetylation. Sirtuin 1 (SIRT1) is a deacetylase and is decreased in DKD, which indicates that it may regulate Txnip in this disease. Here, we used whole-body heterozygous Sirt1 knockout (Sirt1
Identifiants
pubmed: 37742607
pii: S0753-3322(23)01313-6
doi: 10.1016/j.biopha.2023.115515
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
115515Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier Masson SAS.. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare no conflicts of interest, no use of AI nor AI-assisted technologies in the writing process.