Reversibility of microtubule inhibitor-induced transganglionic degenerative atrophy of central terminals of primary nociceptive neurons

Neuroscience. 1982 May;7(5):1149-54. doi: 10.1016/0306-4522(82)91122-8.

Abstract

Microtubule inhibitor Vinca alkaloids applied around a peripheral nerve induce transganglionic degenerative atrophy of the central terminals of primary nociceptive neurons. This effect is reversible: 40-50 days later the original histochemical structure of the central terminals is restored. Restoration of fluoride-resistant acid phosphatase activity (the marker enzyme of primary nociceptive neurons) in the Rolando substance is due to regenerative sprouting of the formerly atrophied central terminals. Since peripherally-applied Vinca alkaloids induce transganglionic degenerative atrophy of the central terminals without inducing Wallerian degeneration of the peripheral nerve, and since this effect (virtually a synaptic uncoupling) is only temporary, this approach may be used in the treatment of otherwise intractable neuralgias without inducing irreparable alterations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Phosphatase / metabolism
  • Animals
  • Atrophy
  • Axonal Transport / drug effects
  • Axons / drug effects
  • Female
  • Fluorides / pharmacology
  • Ganglia, Spinal / drug effects*
  • Interneurons / drug effects
  • Male
  • Microtubules / drug effects*
  • Nerve Degeneration / drug effects*
  • Nerve Regeneration / drug effects
  • Neurons / drug effects
  • Nociceptors / drug effects*
  • Rats
  • Sciatic Nerve / drug effects*
  • Vinblastine / pharmacology
  • Vinca Alkaloids / pharmacology
  • Vincristine / pharmacology

Substances

  • Vinca Alkaloids
  • leurosine
  • Vincristine
  • Vinblastine
  • Acid Phosphatase
  • Fluorides