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Vol. 55, Issue 3, 584-593, March 1999
Departments of
Entomology and Neuroscience, University of
California, Riverside, California (D.L., M.E.A.);
Department of
Entomology, University of Arizona Tucson, Arizona (Y.P.); and
Department of Entomology, Clemson University, Clemson, South Carolina
(T.M.B.)
Genetic resistance to pyrethroid insecticides involves nervous system
insensitivity linked to regulatory and structural genes of
voltage-sensitive sodium channels. We examined the properties and
relative density of sodium channels in central neurons of susceptible
and pyrethroid-resistant (Pyr-R) insects that were homozygous for the
amino acid substitution V421M in the I-S6 transmembrane segment.
Pyr-R sodium channels show ~21-fold lower sensitivity to the
synthetic pyrethroid permethrin and a ~2-fold increased sensitivity
to the
-scorpion toxin Lqh
IT. Pyr-R channels also exhibit altered
gating properties, including a ~13 mV positive shift in
voltage-dependent activation and ~7 mV positive shift in steady-state
inactivation. Consistent with these changes in gating behavior, Pyr-R
central neurons are less excitable, as evidenced by an ~11 mV
elevation of action potential threshold. No differences in sodium
channel density are evident. The altered properties of Pyr-R sodium
channels provide a plausible molecular basis for nervous system
insensitivity associated with pyrethroid resistance.
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