Journal
BRITISH JOURNAL OF PHARMACOLOGY
Volume 131, Issue 2, Pages 245-254Publisher
WILEY
DOI: 10.1038/sj.bjp.0703595
Keywords
S-oxybutynin; terodiline; papillary muscles; ventricular myocytes; cardiac action potentials; cardiac membrane currents; delayed-rectifier K+ currents; calcium current; action potential duration; rate dependence
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1 The cardiac electrophysiological effects of S-oxybutynin, a single-enantiomer drug under evaluation for the management of urinary incontinence, have been investigated and compared with those of terodiline, an incontinence agent withdrawn following reports of QT lengthening and ventricular tachyarrhythmia. Membrane currents were recorded from whole-cell configured guineapig and rabbit ventricular myocytes, and action potentials were recorded from guinea-pig and rabbit papillary muscles. 2 L-type Ca2+ current (I-Ca,I-L), rapidly-activating K+ current (I-Kr) and slowly-activating K+ current (I-Ks) were unaffected by submicromolar S-oxybutynin and inhibited by higher concentrations; IC50 values were 17.8 mu M for I-Ca,L, 12 mu M for I-Kr, and 41 mu M for I-Ks. Terodiline IC50 values were somewhat lower for I-Ca,I-L (15.2 mu M) and I-Ks (30 mu M), but 24 fold lower in the case of I-Kr (0.5 mu M). 3 The durations of action potentials in guinea-pig and rabbit papillary muscles driven at 1 Hz were unaffected or moderately shortened by 0.1-100 mu M S-oxybutynin, but lengthened by terodiline. Terodiline (less than or equal to 10 mu M) also depressed maximal upstroke velocity. 4 The action potential plateau shortened by an average of 23% when control rabbit papillary muscles were driven at 0.4 Hz instead of 1 Hz. Plateau shortening was significantly smaller in the presence of drugs (30 mu M S-oxybutynin, 3 and 30 mu M terodiline), suggesting that they suppress the transient outward current (I-to) involved in rate-dependent shortening. In experiments on rabbit ventricular myocytes, 3 and 30 mu M S-oxybutynin inhibited I-to by 9+/-2% and 35+3%, respectively, whereas 3 and 30 mu M terodiline inhibited the current by 31+/-3% and 87+/-3%, respectively. 5 The results indicate that S-oxybutynin has relatively weak non-specific effects on cardiac ion channels, and that clinically relevant submicromolar concentrations are unlikely to have terodiline-like proarrhythmic actions on the myocardium.
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