-blocking properties of drugs.-blockers E-4031 (0.001–0.1 µM, n = 9/7) or erythromycin (1–300 µM, n = 9/7) and APD, APD dispersion, and triangulation were analyzed.At baseline, APD was longer in LQT1 than in LMC rabbits in LV apex and RV mid. Erythromycin and E-4031 prolonged APD in LQT1 and LMC rabbits in all positions. However, erythromycin-induced percentaged APD prolongation related to baseline (%APD) was more pronounced in LQT1 at LV base-lateral and RV mid positions (100 µM, LQT1, +40.6±9.7% vs. LMC, +24.1±10.0%, p<0.05) and E-4031-induced %APD prolongation was more pronounced in LQT1 at LV base-lateral (0.01 µM, LQT1, +29.6±10.6% vs. LMC, +19.1±3.8%, p<0.05) and LV base-septal positions. Moreover, erythromycin significantly increased...
<p><b><i>A</i></b>, effects of I<sub>Kr</sub>/HERG blocker dofetilide (Dof, 10 nM) on I<sub>HERG</su...
BACKGROUND – Terfenadine was withdrawn because of proarrhythmia. Its therapeutic anti-histamine conc...
UTT780 is a low molecular weight irreversible inhibitor of myeloperoxidase investigated as a potenti...
-blocking properties of drugs.-blockers E-4031 (0.001–0.1 µM, n = 9/7) or erythromycin (1–300 µM, n ...
Prolongation of action potential duration (APD), increased spatial APD dispersion, and triangulation...
Background: Prolongation of action potential duration (APD), increased spatial APD dispersion, and t...
<p>Exemplary, representative MAP triangulation in (A) LQT1 and LMC rabbit at baseline. Exemplary, re...
<p>Exemplary, representative MAP in (A) LQT1 and (B) LMC rabbits at baseline and at different concen...
<p>Differences of spatial dispersion of action potential duration (APD<sub>75</sub>) between LQT1 (n...
The purpose of the present study was to comparatively evaluate human HERG currents and QT intervals ...
The purpose of the present study was to comparatively evaluate human HERG currents and QT intervals ...
Background. Erythromycin is known to prolong ventricular repolarization and has been associated with...
The purpose of the present study was to comparatively evaluate human HERG currents and QT intervals ...
Block of human ether-a-go-go related gene (hERG) K+ channels by otherwise useful drugs is the most c...
A variety of different drugs block cardiac IKr-currents thus causing a serious side effect, the so c...
<p><b><i>A</i></b>, effects of I<sub>Kr</sub>/HERG blocker dofetilide (Dof, 10 nM) on I<sub>HERG</su...
BACKGROUND – Terfenadine was withdrawn because of proarrhythmia. Its therapeutic anti-histamine conc...
UTT780 is a low molecular weight irreversible inhibitor of myeloperoxidase investigated as a potenti...
-blocking properties of drugs.-blockers E-4031 (0.001–0.1 µM, n = 9/7) or erythromycin (1–300 µM, n ...
Prolongation of action potential duration (APD), increased spatial APD dispersion, and triangulation...
Background: Prolongation of action potential duration (APD), increased spatial APD dispersion, and t...
<p>Exemplary, representative MAP triangulation in (A) LQT1 and LMC rabbit at baseline. Exemplary, re...
<p>Exemplary, representative MAP in (A) LQT1 and (B) LMC rabbits at baseline and at different concen...
<p>Differences of spatial dispersion of action potential duration (APD<sub>75</sub>) between LQT1 (n...
The purpose of the present study was to comparatively evaluate human HERG currents and QT intervals ...
The purpose of the present study was to comparatively evaluate human HERG currents and QT intervals ...
Background. Erythromycin is known to prolong ventricular repolarization and has been associated with...
The purpose of the present study was to comparatively evaluate human HERG currents and QT intervals ...
Block of human ether-a-go-go related gene (hERG) K+ channels by otherwise useful drugs is the most c...
A variety of different drugs block cardiac IKr-currents thus causing a serious side effect, the so c...
<p><b><i>A</i></b>, effects of I<sub>Kr</sub>/HERG blocker dofetilide (Dof, 10 nM) on I<sub>HERG</su...
BACKGROUND – Terfenadine was withdrawn because of proarrhythmia. Its therapeutic anti-histamine conc...
UTT780 is a low molecular weight irreversible inhibitor of myeloperoxidase investigated as a potenti...