Channelpedia

PubMed 20858500


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: KCNQ1 , KChip2a , Kv1.4 , Kv1.5 , Kv3.1 , Kv4.3 , Kv7.1 , Slo1



Title: Celecoxib blocks cardiac Kv1.5, Kv4.3 and Kv7.1 (KCNQ1) channels: effects on cardiac action potentials.

Authors: Alvaro Macías, Cristina Moreno, Javier Moral-Sanz, Angel Cogolludo, Miren David, Matteo Alemanni, Francisco Pérez-Vizcaino, Antonio Zaza, Carmen Valenzuela, Teresa Gonzalez

Journal, date & volume: J. Mol. Cell. Cardiol., 2010 Dec , 49, 984-92

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20858500


Abstract
Celecoxib is a COX-2 inhibitor that has been related to an increased cardiovascular risk and that exerts several actions on different targets. The aim of this study was to analyze the effects of this drug on human cardiac voltage-gated potassium channels (Kv) involved on cardiac repolarization Kv1.5 (I(Kur)), Kv4.3+KChIP2 (I(to1)) and Kv7.1+KCNE1 (I(Ks)) and to compare with another COX-2 inhibitor, rofecoxib. Currents were recorded in transfected mammalian cells by whole-cell patch-clamp. Celecoxib blocked all the Kv channels analyzed and rofecoxib was always less potent, except on Kv4.3+KChIP2 channels. Kv1.5 block increased in the voltage range of channel activation, decreasing at potentials positive to 0 mV. The drug modified the activation curve of the channels that became biphasic. Block was frequency-dependent, increasing at fastest frequencies. Celecoxib effects were not altered by TEA(out) in R487Y mutant Kv1.5 channels but the kinetics of block were slower and the degree of block was smaller with TEA(in), indicating that celecoxib acts from the cytosolic side. We confirmed the blocking properties of celecoxib on native Kv currents from rat vascular cells, where Kv1.5 are the main contributors (IC(50)≈ 7 μM). Finally, we demonstrate that celecoxib prolongs the action potential duration in mouse cardiac myocytes and shortens it in guinea pig cardiac myocytes, suggesting that Kv block induced by celecoxib may be of clinical relevance.