Propofol inhibits prokaryotic voltage-gated Na⁺ channels by promoting activation-coupled inactivation.

ABSTRACT: Propofol is widely used in the clinic for the induction and maintenance of general anesthesia. As with most general anesthetics, however, our understanding of its mechanism of action remains incomplete. Local and general anesthetics largely inhibit voltage-gated Na⁺ channels (Navs) by inducing an apparent stabilization of the inactivated state, associated in some instances with pore block. To determine the biophysical and molecular basis of propofol action in Navs, we investigated NaChBac and NavMs, two prokaryotic Navs with distinct voltage dependencies and gating kinetics, by whole-cell patch clamp electrophysiology in the absence and presence of propofol at clinically relevant concentrations (2-10 µM). In both Navs, propofol induced a hyperpolarizing shift of the pre-pulse in

SUBMITTER: Yang E 

PROVIDER: S-EPMC6122921 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature