The effect of spider toxin PhTx3-4, ω-conotoxins MVIIA and MVIIC on glutamate uptake and on capsaicin-induced glutamate release and [Ca2+]i in spinal cord synaptosomes

Cell Mol Neurobiol. 2011 Mar;31(2):277-83. doi: 10.1007/s10571-010-9618-5.

Abstract

In spinal cord synaptosomes, the spider toxin PhTx3-4 inhibited capsaicin-stimulated release of glutamate in both calcium-dependent and -independent manners. In contrast, the conus toxins, ω-conotoxin MVIIA and xconotoxin MVIIC, only inhibited calcium-dependent glutamate release. PhTx3-4, but not ω-conotoxin MVIIA or xconotoxin MVIIC, is able to inhibit the uptake of glutamate by synaptosomes, and this inhibition in turn leads to a decrease in the Ca(2+)-independent release of glutamate. No other polypeptide toxin so far described has this effect. PhTx3-4 and ω-conotoxins MVIIC and MVIIA are blockers of voltage-dependent calcium channels, and they significantly inhibited the capsaicin-induced rise of intracellular calcium [Ca(2+)](i) in spinal cord synaptosomes, which likely reflects calcium entry through voltage-gated calcium channels. The inhibition of the calcium-independent glutamate release by PhTx3-4 suggests a potential use of the toxin to block abnormal glutamate release in pathological conditions such as pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Capsaicin / pharmacology*
  • Fluorescence
  • Glutamic Acid / metabolism*
  • Male
  • Neuropeptides / toxicity*
  • Rats
  • Rats, Wistar
  • Spider Venoms / toxicity
  • Spinal Cord / drug effects
  • Spinal Cord / metabolism*
  • Synaptosomes / drug effects
  • Synaptosomes / metabolism*
  • omega-Conotoxins / toxicity*

Substances

  • Neuropeptides
  • Spider Venoms
  • Tx3 neurotoxin
  • omega-Conotoxins
  • omega-conotoxin-MVIIC
  • Glutamic Acid
  • ziconotide
  • Capsaicin
  • Calcium