Article date: October 1994
By: F.G. Lorenzi, T.R. Bridal, W. Spinelli, in Volume 113, Issue 2, pages 527-535
We investigated the effects of two 5‐HT3 antagonists, ondansetron and granisetron, on the action potential duration (APD) and the delayed rectifier current (IK) of feline isolated ventricular myocytes. Whole‐cell current and action potential recordings were performed at 37°C with the patch clamp technique.
Ondansetron and granisetron blocked IK with a KD of 1.7 ± 1.0 and 4.3 ± 1.7 μm, respectively. At a higher concentration (30 μm), both drugs blocked the inward rectifier (IK1).
The block of IK was dependent on channel activation. Both drugs slowed the decay of IK tail currents and produced a crossover with the pre‐drug current trace. These results are consistent with block and unblock from the open state of the channel.
Granisetron showed an intrinsic voltage‐dependence as the block increased with depolarization. The equivalent voltage‐dependency of block (δ) was 0.10 ± 0.04, suggesting that granisetron blocks from the intracellular side at a binding site located 10% across the transmembrane electrical field.
Ondansetron (1 μm) and granisetron (3 μm) prolonged APD by about 30% at 0.5 Hz. The prolongation of APD by ondansetron was abolished at faster frequencies (3 Hz) showing reverse rate dependence.
In conclusion, the 5‐HT3 antagonists, ondansetron and granisetron, are open state blockers of the ventricular delayed rectifier and show a clear class III action.
We investigated the effects of two 5‐HT3 antagonists, ondansetron and granisetron, on the action potential duration (APD) and the delayed rectifier current (IK) of feline isolated ventricular myocytes. Whole‐cell current and action potential recordings were performed at 37°C with the patch clamp technique.
Ondansetron and granisetron blocked IK with a KD of 1.7 ± 1.0 and 4.3 ± 1.7 μm, respectively. At a higher concentration (30 μm), both drugs blocked the inward rectifier (IK1).
The block of IK was dependent on channel activation. Both drugs slowed the decay of IK tail currents and produced a crossover with the pre‐drug current trace. These results are consistent with block and unblock from the open state of the channel.
Granisetron showed an intrinsic voltage‐dependence as the block increased with depolarization. The equivalent voltage‐dependency of block (δ) was 0.10 ± 0.04, suggesting that granisetron blocks from the intracellular side at a binding site located 10% across the transmembrane electrical field.
Ondansetron (1 μm) and granisetron (3 μm) prolonged APD by about 30% at 0.5 Hz. The prolongation of APD by ondansetron was abolished at faster frequencies (3 Hz) showing reverse rate dependence.
In conclusion, the 5‐HT3 antagonists, ondansetron and granisetron, are open state blockers of the ventricular delayed rectifier and show a clear class III action.
DOI: 10.1111/j.1476-5381.1994.tb17021.x
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