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. Author manuscript; available in PMC: 2007 Aug 27.
Published in final edited form as: Anesthesiology. 2007 Jul;107(1):82–90. doi: 10.1097/01.anes.0000267502.18605.ad

Figure 2. Minimal or no block of resting and inactivated Na+ channels by 10 μM BLA.

Figure 2

(A) Superimposed traces of Na+ currents were recorded before and 5 minutes after application of 10 μM BLA. For the resting block by BLA, the cell was held at −140 mV and stimulated once every 30 s by a brief test pulse (+50 mV for 3 ms; inset). (B) For the inactivated block by BLA, the cell was depolarized to −70 mV for 10 s (inset), which provided sufficient time for inactivated Na+ channels to interact with BLA. Superimposed traces of Na+ currents before and after application of 10 μM BLA were recorded by a brief test pulse. An interpulse (−140 mV for 100 ms; inset), which allowed drug-free inactivated Na+ channels to recover, was applied before the brief test pulse. Again, the inactivated block by BLA was minimal.