Inactivation-Deficient Human Skeletal Muscle Na⁺ Channels (hNav1.4-L443C/A444W) in Stably Transfected HEK-293 Cells

Abstract

After transient transfection of an hNav1.4-L443C/A444W mutant clone, HEK-293 cells exhibited large inactivation-deficient Na⁺ currents. We subsequently established a stable cell line expressing robust inactivation-deficient Na⁺ currents. Persistent late Na⁺ currents were far more sensitive to block by class 1 anti-arrhythmic flecainide, mexiletine, propafenone, and amiodarone at 10 μ M than peak Na⁺ currents. Such results support a hypothesis that persistent late Na⁺ currents are in vivo targets for class 1 anti-arrhythmic drugs at their therapeutic plasma concentrations. Stably transfected HEK-293 cells expressing robust inactivation-deficient Na⁺ currents will likely be suitable for screening novel drugs that target persistent late Na⁺ currents selectively.

• Class 1 Antiarrhythmic Agent
• Persistent Late Current
• Sodium Channel
• Stable Cell Line