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. 2003 Nov 7;556(Pt 1):109–120. doi: 10.1113/jphysiol.2003.055012

Figure 11. The ability of quinidine to increase the rate of inactivation in fKv1.4[V561A]ΔN channels is [K+]o independent.

Figure 11

A, in the presence of 2 mm[K+]o, τinactivation,2K= 2.164 ± 0.135 s. Addition of 1 mm quinidine increases the rate of inactivation to τinactivation,2K,1mMQ= 1.706 ± 0.132 s. B, in the presence of 98 mm[K+]o,τinactivation,98K= 1.529 ± 0.066. The addition of 1 mm quinidine further increases the rate of inactivation: τinactivation,98K,1mMQ= 1.300 ± 0.079 s.