Key result
Ketanserin prolongs APD and reduces IKr in cardiomyocytes via its benzoyl-piperidine moiety.
Population
Guinea pig isolated papillary muscles and isolated myocytes
Design
Preclinical
Authors
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May warrant QT monitoring with ketanserin; leaves open human translation and class effects of benzoyl-piperidine compounds.
Ketanserin-induced action potential prolongation and arrhythmogenicity are mediated by direct blockade of myocardial potassium channels (IKr) via its benzoyl-piperidine moiety, not by 5-HT2A/2C receptor antagonism.
Grand et al. (1995) studied this question. Ketanserin was evaluated on Action potential duration (APD) lengthening and potassium current (IKr) reduction. Ketanserin prolonged action potential duration and reduced the IKr component of the delayed outward current in guinea pig cardiomyocytes, an effect mediated by its benzoyl-piperidine moiety.
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