Cholesterol and Cholesterol-Derived Molecules Differentially Modulate Neuronal Kv7.2/7.3 Channels.Open Access

Karabatak E; Nematswerani R; Meiritz V; Rychlik N; Seebohm G; Glorius F; Budde T

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Kv7 potassium channels generate slowly activating, non-inactivating outward potassium currents and are critical regulators of cellular excitability. While cholesterol is known to modulate multiple ion channels, its concentration-dependent effects and the influence of cholesterol-derived molecules on Kv7 channels remain insufficiently characterized. In this study, we investigated the effects of cholesterol and cholesterol-derived molecules, including steroid hormones and chemically modified imidazolium-based cholesterol derivatives (CHIMs) on Kv7.2/7.3 channels heterologously expressed in HEK293FT cells using conventional whole-cell patch-clamp recordings. Application of high cholesterol concentrations (1 mM) significantly reduced Kv7.2/7.3 current amplitudes over a wide range of potentials without changing voltage-dependent current characteristics. CHIMs also reduced currents, whereas a fluorescent derivative, CHIM-L-NBD, unexpectedly enhanced Kv7.2/7.3 currents. In contrast, the NBD moiety alone had no effect. Progesterone and 17β-estradiol inhibition of Kv7.2/7.3 currents was most evident at strongly depolarized potentials. For progesterone this was associated with a change in the slope of the activation curve. These findings demonstrate that Kv7.2/7.3 channels respond differentially to structural modifications of cholesterol and to steroid hormones thereby suggesting that different cholesterol-derived molecules may serve as tool compounds with potentially opposing modulatory effects on Kv7.2/7.3 channels.

Details zur Publikation

FachzeitschriftArchiv der Pharmazie / Chemistry in Life Sciences (ArchPharm)
Jahrgang / Bandnr. / Volume359
Ausgabe / Heftnr. / Issue6
Artikelnummere70280
StatusVeröffentlicht
Veröffentlichungsjahr2026 (30.06.2026)
Sprache, in der die Publikation verfasst istEnglisch
StichwörterHumans; Cholesterol; HEK293 Cells; KCNQ3 Potassium Channel; KCNQ2 Potassium Channel; Dose-Response Relationship, Drug; Patch-Clamp Techniques; Structure-Activity Relationship; Neurons; Progesterone; Estradiol

Autor*innen der Universität Münster

Budde, Thomas
Glorius, Frank
Karabatak, Elif
Rychlik, Nicole
Seebohm, Guiscard