Selective and state-dependent activation of TRESK (K2P 18.1) background potassium channel by cloxyquin.
Miklós LengyelAlice DobolyiGábor Á CzirjákPéter EnyediPublished in: British journal of pharmacology (2017)
Cloxyquin activates TRESK by a Ca2+ /calcineurin-independent mechanism. The drug is specific for TRESK within the K2P channel family and useful for studying TRESK currents in native cells. The state-dependent pharmacological profile of this channel should be considered in the development of therapeutics for migraine and other nociceptive disorders.