Novel paradigms on scorpion toxins that affects the activating mechanism of sodium channels

Toxicon. 2007 Feb;49(2):171-80. doi: 10.1016/j.toxicon.2006.09.016. Epub 2006 Sep 27.

Abstract

Scorpion toxins classified as beta-class are reviewed using a new paradigm. Four distinct sub types are recognized: "classical", "Tsgamma-like", "excitatory" and "depressant"beta-scorpion toxins. Recent experimental data have made possible to identify the interacting interfaces of the Na(+) channel-receptor site 4 with some of these toxins. The voltage-sensor trapping mechanism proposed for the action of these toxic peptides is analyzed in the context of what causes a modification of the activating mechanism of Na(+) channels. A cartoon model is presented with the purpose of summarizing the most current knowledge on the field. Finally, the recent advances on the knowledge of the specific interactions of beta-toxins and different sub types of Na(+) channels are also reviewed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Humans
  • Ion Channel Gating* / drug effects
  • Ion Channel Gating* / physiology
  • Scorpion Venoms / pharmacology*
  • Sodium Channel Blockers / pharmacology*
  • Sodium Channels / drug effects*
  • Voltage-Gated Sodium Channel beta-4 Subunit

Substances

  • SCN4B protein, human
  • Scorpion Venoms
  • Sodium Channel Blockers
  • Sodium Channels
  • Voltage-Gated Sodium Channel beta-4 Subunit