Uptake-leak balance of SR Ca
Arrhythmia
Calcium signaling
Catecholaminergic polymorphic ventricular tachycardia
Channelopathy
Ryanodine receptor
Sarcoplasmic reticulum calcium pump
Journal
Journal of molecular and cellular cardiology
ISSN: 1095-8584
Titre abrégé: J Mol Cell Cardiol
Pays: England
ID NLM: 0262322
Informations de publication
Date de publication:
09 2022
09 2022
Historique:
received:
24
08
2021
revised:
01
04
2022
accepted:
22
05
2022
pubmed:
2
6
2022
medline:
24
8
2022
entrez:
1
6
2022
Statut:
ppublish
Résumé
Mutations of the RyR2 are channelopathies that can predispose to life threatening catecholaminergic polymorphic ventricular tachycardias (CPVTs) during exercise or stress. However, the cellular and molecular mechanisms that are causal for the arrhythmias downstream of the β-adrenergic receptor (β-AR) activation are not defined. They may be specific and different for each particular RyR2 mutation. Obvious possibilities are the phosphorylation of the mutated RyR2s or the stimulation of the SR Ca
Identifiants
pubmed: 35644481
pii: S0022-2828(22)00104-3
doi: 10.1016/j.yjmcc.2022.05.011
pii:
doi:
Substances chimiques
Ryanodine Receptor Calcium Release Channel
0
Isoproterenol
L628TT009W
Calcium
SY7Q814VUP
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-14Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.