Inhibition of Kir4.1 potassium channels by quinacrine
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Inwardly rectifying potassium (Kir) channels are expressed in many cell types and contribute to a wide range of physiological processes. Particularly, Kir4.1 channels are involved in the astroglial spatial potassium buffering. In this work, we examined the effects of the cationic amphiphilic drug quinacrine on Kir4.1 channels heterologously expressed in HEK293 cells, employing the patch clamp technique. Quinacrine inhibited the currents of Kir4.1 channels in a concentration and voltage dependent manner. In inside-out patches, quinacrine inhibited Kir4.1 channels with an IC50 value of 1.8 ± 0.3 μM and with extremely slow blocking and unblocking kinetics. Molecular modeling combined with mutagenesis studies suggested that quinacrine blocks Kir4.1 by plugging the central cavity of the channels, stabilized by the residues E158 and T128. Overall, this study shows that quinacrine blocks Kir4.1 channels, which would be expected to impact the potassium transport in several tissues. © 2017 Elsevier B.V.
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Cationic amphiphilic drugs; Kir4.1 channels; Quinacrine inwardly rectifying potassium channel subunit Kir4.1; mepacrine; potassium channel; unclassified drug; inwardly rectifying potassium channel; mepacrine; potassium; potassium channel; Article; concentration response; controlled study; HEK293 cell line; human; human cell; IC50; molecular model; mutagenesis; priority journal; protein expression; protein transport; animal; antagonists and inhibitors; astrocyte; channel gating; drug effects; metabolism; patch clamp technique; physiology; procedures; rat; Animals; Astrocytes; HEK293 Cells; Humans; Ion Channel Gating; Patch-Clamp Techniques; Potassium; Potassium Channels; Potassium Channels, Inwardly Rectifying; Quinacrine; Rats
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