Lidocaine: A Foot in the Door of the Inner Vestibule Prevents Ultra-Slow Inactivation of a Voltage-Gated Sodium Channel

• Published in: Molecular pharmacology 2004-09, Vol.66 (3), p.648
• Main Authors: Sandtner, Walter, Szendroedi, Julia, Zarrabi, Touran, Zebedin, Eva, Hilber, Karlheinz, Glaaser, Ian, Fozzard, Harry A, Dudley, Samuel C, Todt, Hannes
• Format: Article
• Language: English
• Subjects: Amino Acid Substitution; Animals; Binding Sites; Electrophysiology; Glutamic Acid - genetics; Lidocaine - pharmacology; Lysine - genetics; Mutagenesis, Site-Directed; Oocytes - drug effects; Oocytes - metabolism; Sodium Channel Blockers - pharmacology; Sodium Channels - chemistry; Sodium Channels - genetics; Sodium Channels - metabolism; Sodium Channels - physiology; Xenopus laevis
• ISSN: 0026-895X; 1521-0111

After opening, Na + channels may enter several kinetically distinct inactivated states. Whereas fast inactivation occurs by occlusion of the inner channel pore by the fast inactivation gate, the mechanistic basis of slower inactivated states is much less clear. We have recently suggested that the inner pore of the voltage-gated Na + channel may be involved in the process of ultra-slow inactivation (I US ). The local anesthetic drug lidocaine is known to bind to the inner vestibule of the channel and to interact with slow inactivated states. We therefore sought to explore the effect of lidocaine binding on I US . rNa V 1.4 channels carrying the mutation K1237E in the selectivity filter were driven into I US by long depolarizing pulses (–20 mV, 300 s). After repolarization to –120 mV, 53 ± 5% of the channels recovered with a very slow time constant (τ rec = 171 ± 19 s), typical for recovery from I US . After exposure to 300 μM lidocaine, the fraction of channels recovering from I US was reduced to 13 ± 4% ( P < 0.01, n = 6). An additional mutation in the binding site of lidocaine (K1237E + F1579A) substantially reduced the effect of lidocaine on I US , indicating that lidocaine has to bind to the inner vestibule of the channel to modulate I US . We propose that I US involves a closure of the inner vestibule of the channel. Lidocaine may interfere with this pore motion by acting as a “foot in the door” in the inner vestibule.