Inactivation of Native K Channels

We have experimented with isolated cardiomyocytes of mollusks Helix . During the whole-cell patch-clamp recordings of K + currents a considerable decrease in amplitude was observed upon repeated voltage steps at 0.96 Hz. For these experiments, ventricular cells were depolarized to identical + 20 mV...

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Veröffentlicht in:The Journal of membrane biology 2022-02, Vol.255 (1), p.13-31
Hauptverfasser: Kodirov, Sodikdjon A., Brachmann, Johannes, Safonova, Tatiana A., Zhuravlev, Vladimir L.
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Sprache:eng
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Zusammenfassung:We have experimented with isolated cardiomyocytes of mollusks Helix . During the whole-cell patch-clamp recordings of K + currents a considerable decrease in amplitude was observed upon repeated voltage steps at 0.96 Hz. For these experiments, ventricular cells were depolarized to identical + 20 mV from a holding potential of − 50 mV. The observed spontaneous inhibition of outward currents persisted in the presence of 4-aminopyridine, tetraethylammonium chloride or E-4031, the selective class III antiarrhythmic agent that blocks HERG channels. Similar tendency was retained when components of currents sensitive to either 4-AP or TEA were mathematically subtracted. Waveforms of currents sensitive to 1 and 10 micromolar concentration of E-4031 were distinct comprising prevailingly those activated during up to 200 ms pulses. The outward current activated by a voltage ramp at 60 mV x s −1 rate revealed an inward rectification around + 20 mV. This feature closely resembles those of the mammalian cardiac delayed rectifier I Kr . Graphic Abstract
ISSN:0022-2631
1432-1424
DOI:10.1007/s00232-021-00195-w