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Published on: April 6, 2014
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.
Abstract:
Following neurotrauma, cells beyond the initial trauma site undergo secondary degeneration, with excess Ca2+ a likely trigger for loss of neurons, compact myelin and function. Treatment using inhibitors of specific Ca2+ channels has shown promise in preclinical studies, but clinical trials have been disappointing and combinatorial approaches are needed. We assessed efficacy of multiple combinations of three Ca2+ channel inhibitors at reducing secondary degeneration following partial optic nerve transection in rat. We used lomerizine to inhibit voltage gated Ca2+ channels; oxidised adenosine-triphosphate (oxATP) to inhibit purinergic P2X7 receptors and/or 2-[7-(1H-imidazol-1-yl)-6-nitro-2,3-dioxo-1,2,3,4-tetrahydro quinoxalin-1-yl]acetic acid (INQ) to inhibit Ca2+ permeable α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. Only the three Ca2+ channel inhibitors delivered in combination significantly preserved visual function, as assessed using the optokinetic nystagmus visual reflex, at 3 months after injury. Preservation of retinal ganglion cells was partial and is unlikely to have accounted for differential effects on function. A range of the Ca2+ channel inhibitor combinations prevented swelling of optic nerve vulnerable to secondary degeneration. Each of the treatments involving lomerizine significantly increased the proportion of axons with normal compact myelin. Nevertheless, limiting decompaction of myelin was not sufficient for preservation of function in our model. Multiple combinations of Ca2+ channel inhibitors reduced formation of atypical node/paranode complexes; outcomes were not associated with preservation of visual function. However, prevention of lengthening of the paranodal gap that was only achieved by treatment with the three Ca2+ channel inhibitors in combination was an important additional effect that likely contributed to the associated preservation of the optokinetic reflex using this combinatorial treatment strategy.
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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