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Inhibition of lysosomal degradation rescues pentamidine-mediated decreases of K(IR)2.1 ion channel expression but not that of K(v)11.1

Publikace na 1. lékařská fakulta, Lékařská fakulta v Plzni |
2011

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

Pentamidine disrupt trafficking of two structurally different potassium channels, which can precipitate life-threatening arrhythmia. We demonstrate that a single drug can interfere in cardiac potassium channel trafficking in a subtype specific mode and that this adverse drug effect can be corrected in a channel specific manner.