Inhibition of cardiac K
Animals
Anti-Arrhythmia Agents
/ pharmacology
Female
Heart Ventricles
/ metabolism
Humans
Lidocaine
/ pharmacology
Male
Mexiletine
/ pharmacology
Oocytes
Potassium Channel Blockers
/ pharmacology
Protein Isoforms
/ antagonists & inhibitors
Shal Potassium Channels
/ antagonists & inhibitors
Xenopus laevis
Action potential
Heart failure
K(v)4.3 channel
Lidocaine
Mexiletine
Ventricular tachycardia
Journal
European journal of pharmacology
ISSN: 1879-0712
Titre abrégé: Eur J Pharmacol
Pays: Netherlands
ID NLM: 1254354
Informations de publication
Date de publication:
05 Aug 2020
05 Aug 2020
Historique:
received:
30
10
2019
revised:
01
04
2020
accepted:
23
04
2020
pubmed:
4
5
2020
medline:
25
3
2021
entrez:
4
5
2020
Statut:
ppublish
Résumé
Transient outward K
Identifiants
pubmed: 32360350
pii: S0014-2999(20)30251-X
doi: 10.1016/j.ejphar.2020.173159
pii:
doi:
Substances chimiques
Anti-Arrhythmia Agents
0
Potassium Channel Blockers
0
Protein Isoforms
0
Shal Potassium Channels
0
Mexiletine
1U511HHV4Z
Lidocaine
98PI200987
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
173159Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest A.K.R. reports educational support from Boston Scientific and Medtronic. D.T. reports receiving lecture fees/honoraria from Bayer Vital, Boehringer Ingelheim Pharma, Bristol-Myers Squibb, Daiichi Sankyo, Medtronic, Pfizer Pharma, Sanofi-Aventis, St. Jude Medical and ZOLL CMS. P.L. reports receiving lecture fees from Bayer Vital and Pfizer Pharma and educational support from Boston Scientific and Johnson & Johnson. B.S. reports personal fees for surgical proctoring services from Abbott. The remaining authors have reported that they have no relationships relevant to the content of this paper to disclose.