C. Ulens et al., Norporpoxyphene-induced cardiotoxicity is associated with changes in ion-selectivity and gating of HERG currents, CARDIO RES, 44(3), 1999, pp. 568-578
Citations number
24
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective: Norpropoxyphene (NP) is a major metabolite of propoxyphene (P),
a relatively weak mu-opioid receptor agonist. Toxic blood concentrations ra
nging from 3 to 180 mu mol/l have been reported and the accumulation of NP
in cardiac tissue leads to naloxone-insensitive cardiotoxicity. Since sever
al lines of evidence suggest that not only block of I-Na but also I-K block
may contribute to the non-opioid cardiotoxic effects of P and NP, we inves
tigated the effects of P and NP on HERG channels. HERG presumably encodes I
-Kr, the rapidly-activating delayed rectifier K+ current, which is known to
have an important role in initiating repolarization of action potentials i
n cardiac myocytes. Methods: Using the 2-microelectrode voltage clamp techn
ique we investigated the interaction of P and NP with HERG channels, expres
sed in Xenopus oocytes. Results: Our experiments show that low drug concent
rations (5 mu mol/l) facilitate HERO currents, while higher drug concentrat
ions block HERG currents (IC50-values of approx. 40 mu mol/l) and dramatica
lly shift the reversal potential to a more positive value because of a 30-f
old increased Na+-permeability. P and NP also alter gating of HERG channels
by slowing down channel activation and accelerating channel deactivation k
inetics. The mutant S631C nullifies the effect of P and NP on the channel's
K+-selectivity. Conclusion: P and NP show a complex and unique drug-channe
l interaction, which includes altering ion-selectivity and gating. Site-dir
ected mutagenesis suggests that an interaction with S631 contributes to the
drug-induced disruption of K+-selectivity. No specific role of the minK su
bunit in the HERG block mechanism could be determined. (C) 1999 Elsevier Sc
ience B.V. All rights reserved.