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Epilepsy drug shows promise in protecting nerves from damage in MS

26 January 2016  •  Author: Victoria White

According to a new study from University College London (UCL), an epilepsy drug could lead to a new treatment that protects nerve damage in multiple sclerosis (MS) patients.

ms

The researchers, led by Dr Raj Kapoor from the UCL Institute of Neurology, found the anti-convulsant drug phenytoin protected neural tissue in patients with optic neuritis. Optic neuritis is a symptom of MS which causes the nerves carrying information between the eye to the brain to become inflamed and damaged.

The findings of the study bring researchers one step closer to establishing neuroprotective drugs for people with MS.

As the study looks at repurposing an existing treatment already shown to be clinically effective, the use of phenytoin for MS could potentially have patient benefit in a much shorter timescale than usual.

In the study, 86 people with acute optic neuritis received either phenytoin or a placebo for three months. OCT (Optical Coherence Tomography) was used to measure the thickness of the retina and the light sensitive nerve layer at the back of the eye. At the end of the trial the group who had taken phenytoin had on average 30% less damage to the nerve fibre layer compared with those who received the placebo.

Findings could lead to a new treatment that protects nerves from damage

Dr Kapoor and his team had been focusing on the sodium channel as part of their research into neuroprotection. In inflamed areas, the axons of nerve cells get flooded with sodium, which causes an influx of calcium which in turn causes cell death. If sodium entry into the cell can be blocked there is potential to prevent this.

Dr Kapoor said: “We wanted to find out if the theory that blocking sodium currents, which we developed in basic work over many years, actually served to protect neural tissue – a test-bed to see if we can achieve neuroprotection.”

Optic neuritis, which is often the first symptom of MS, gave the researchers a window of opportunity to study active inflammation early on in the disease process. Changes or damage to the nerves in the eye and the optic nerve are easy to measure.

Dr Kapoor said: “These are promising results and if our findings are confirmed by larger, Phase 3 trials, could lead to a new treatment that protects nerves from the damage caused both in optic neuritis and throughout the central nervous system in other attacks of MS.”

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