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. 1994 Oct;428(3-4):400-9.
doi: 10.1007/BF00724524.

Modification of sodium channel gating and kinetics by versutoxin from the Australian funnel-web spider Hadronyche versuta

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Modification of sodium channel gating and kinetics by versutoxin from the Australian funnel-web spider Hadronyche versuta

G M Nicholson et al. Pflugers Arch. 1994 Oct.

Abstract

The effects of a neurotoxin (versutoxin VTX), purified from the venom of the Australian Blue Mountains funnel-web spider Hadronyche versuta, on the ionic currents in rat dorsal root ganglion cells were investigated under voltage-clamp conditions using the whole-cell patch-clamp technique. VTX had no effect on tetrodotoxin-resistant (TTX-R) sodium currents or potassium currents. In contrast VTX produced a dose-dependent slowing or removal of tetrodotoxin-sensitive (TTX-S) sodium current inactivation, a reduction in peak TTX-S sodium current but did not markedly slow tail current kinetics of TTX-S sodium currents. This steady-state sodium current was maintained during prolonged depolarizations at all test potentials and the reduction in sodium current amplitude produced by VTX had an apparent Ki of 37 nM. In the presence of 32 nM VTX the voltage dependence of steady-state sodium channel inactivation (h infinity) also showed a significant 7 mV shift in the voltage midpoint in the hyperpolarizing direction, with no change in the slope factor. In addition there was a steady-state or non-inactivating component present (14 +/- 2% of maximal sodium current) at prepulse potentials more depolarized than -40 mV, potentials which normally inactivate all TTX-S sodium channels. Finally, there was an observed increase in the rate of recovery from inactivation in the presence of VTX. These selective actions of VTX on sodium channel gating and kinetics are similar to those of alpha-scorpion and sea anemone toxins.

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References

    1. Pflugers Arch. 1981 Aug;391(2):85-100 - PubMed
    1. Biochim Biophys Acta. 1977 May 2;466(3):461-73 - PubMed
    1. Pflugers Arch. 1993 Jun;424(1):15-24 - PubMed
    1. J Pharmacol Exp Ther. 1981 Nov;219(2):464-73 - PubMed
    1. Am J Physiol. 1972 Apr;222(4):850-7 - PubMed

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