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Mexiletine block of disease‐associated mutations in S6 segments of the human skeletal muscle Na + channel
Author(s) -
Takahashi Masanori P.,
Can Stephen C.
Publication year - 2001
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.2001.00701.x
Subject(s) - mexiletine , dissociation constant , missense mutation , mutant , chemistry , myotonia , microbiology and biotechnology , patch clamp , skeletal muscle , mutation , biophysics , biology , endocrinology , medicine , biochemistry , receptor , genetics , gene , myotonic dystrophy
1 Over twenty different missense mutations in the α‐subunit of the adult skeletal muscle Na + channel (hSkM1) have been identified as a cause of myotonia or periodic paralysis. We examined state‐dependent mexiletine block for mutations involving the putative binding site in S6 segments (V445M, S804F, V1293I, V1589M and M1592V). Whole‐cell Na + currents were measured from wild‐type (WT) and mutant channels transiently expressed in HEK cells. 2 Use‐dependent block (10 ms pulses to −10 mV, at 20 Hz) in 100 μ m mexiletine was reduced modestly by mutations in IVS6 (V1589M, M1592V) and enhanced by the mutation in IS6 (V445M). For mutations in IIS6 (S804F) and IIIS6 (V1293I) use‐dependent block was not statistically different from that of wild‐type channels. 3 Resting‐state block (10 ms pulses to −10 mV from −150 mV, at 0.1 Hz) of S6 mutants was comparable to that of WT (dissociation constant for resting channels, K R = 650 ± 40 μ m , n = 9). The S6 mutant with the greatest change in K R was V445M ( K R = 794 ± 45 μ m , n = 5), but this difference was only marginally significant ( P = 0.047 )). 4 A modified technique for estimating local anaesthetic affinity of inactivated channels was developed to reduce errors due to slow inactivation and to failure of drug binding to reach equilibrium. Mexiletine affinity for inactivated channels was reduced by mutations in IVS6 (V1589M: dissociation constant for the inactivated state ( K I ) = 44.7 μ m ; M1592V: K I = 40.0 μ m ) and increased by the mutation in IS6 (V445M: K I = 15.0 μ m ), compared to wild‐type channels ( K I = 28.3 μ m ). 5 We conclude that the disease‐associated S6 mutations in domains I–IV cause at most a 2‐fold change in inactivated state affinity and have even less of an effect on resting block. Model simulations show that the reduced use‐dependent block of IVS6 mutants derives primarily from an increased off‐rate at hyperpolarized potentials, whereas the enhanced use‐dependent block of the IS6 mutant was due to a higher affinity for inactivated V445M channels.