HDAC2-dependent remodeling of K
Action Potentials
Animals
Atrial Fibrillation
/ complications
Disease Models, Animal
Electrophysiological Phenomena
Female
Heart Atria
/ metabolism
Heart Failure
/ complications
Histone Deacetylase 2
/ genetics
Humans
Male
Middle Aged
Small-Conductance Calcium-Activated Potassium Channels
/ genetics
Swine
Atrial fibrillation
Electrophysiology
Epigenetics
Histone deacetylase
K(Ca) channel
Journal
Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521
Informations de publication
Date de publication:
01 Feb 2021
01 Feb 2021
Historique:
received:
19
05
2020
revised:
30
11
2020
accepted:
07
12
2020
pubmed:
15
12
2020
medline:
2
2
2021
entrez:
14
12
2020
Statut:
ppublish
Résumé
Atrial fibrillation (AF) with concomitant heart failure (HF) is associated with prolonged atrial refractoriness. Small-conductance, calcium-activated K HDAC2 and KCNN2/3 transcript levels were quantified in patients with AF and HF, and in a porcine model of atrial tachypacing-induced AF and reduced left ventricular function. Tachypacing and anti-Hdac2 siRNA treatment were employed in HL-1 atrial myocytes to study effects on KCNN2/3 mRNA and K Atrial KCNN2 and KCNN3 expression was reduced in AF/HF patients and in a corresponding pig model. HDAC2 displayed significant downregulation in humans and a tendency towards reduced expression in right atrial tissue of pigs. Tachypacing recapitulated downregulation of Kcnn2/K KCNN2/3 and HDAC2 expression is suppressed in AF complicated by HF. Hdac2 directly regulates Kcnn3 mRNA levels in atrial cells. The mechanistic and therapeutic significance of epigenetic electrophysiological effects in AF requires further validation.
Identifiants
pubmed: 33310041
pii: S0024-3205(20)31645-3
doi: 10.1016/j.lfs.2020.118892
pii:
doi:
Substances chimiques
KCNN2 protein, human
0
KCNN3 protein, human
0
Small-Conductance Calcium-Activated Potassium Channels
0
HDAC2 protein, human
EC 3.5.1.98
Histone Deacetylase 2
EC 3.5.1.98
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
118892Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.