Three Ca2+ channel inhibitors in combination limit chronic secondary degeneration following neurotrauma

Donna L Savigni1, Ryan L O'Hare Doig1, Charis R Szymanski1

  • 1Experimental and Regenerative Neurosciences, The University of Western Australia, Crawley, WA 6009, Australia; School of Animal Biology, The University of Western Australia, Crawley, WA 6009, Australia.

Neuropharmacology
|August 21, 2013
PubMed

Insights

Combinatorial therapy with three calcium channel inhibitors significantly preserves visual function after optic nerve injury by preventing secondary degeneration and maintaining myelin integrity. This approach addresses limitations of previous treatments.

Area of Science:

  • Neuroscience
  • Ophthalmology
  • Pharmacology

Background:

  • Secondary degeneration after neurotrauma causes neuron and myelin loss.
  • Excess intracellular calcium (Ca2+) is a key trigger for this degeneration.
  • Previous single-agent Ca2+ channel inhibitor therapies showed limited clinical success.

Purpose of the Study:

  • To evaluate the efficacy of combinatorial Ca2+ channel inhibitor treatments in reducing secondary degeneration.
  • To identify optimal combinations for preserving visual function after optic nerve injury.

Main Methods:

  • Partial optic nerve transection in a rat model.
  • Administration of three Ca2+ channel inhibitors: lomerizine (voltage-gated), oxATP (P2X7 receptors), and INQ (AMPA receptors).
  • Assessment of visual function using the optokinetic nystagmus reflex at 3 months post-injury.

Main Results:

  • Only the combination of all three inhibitors significantly preserved visual function.
  • Combinations prevented optic nerve swelling and increased axons with compact myelin.
  • Prevention of paranodal gap lengthening by the triple combination correlated with functional preservation.

Conclusions:

  • Combinatorial inhibition of multiple Ca2+ channels is crucial for mitigating secondary degeneration.
  • This strategy offers a promising therapeutic approach for neurotrauma-induced vision loss.
  • Targeting Ca2+ influx through multiple pathways is necessary for effective neuroprotection.

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