image: Research team at the Cumming School of Medicine, from left, pediatric neurologist Dr. Jong Rho; postdoctoral fellow and the study's first author Kingsley Ibhazehiebo; and neuroscientist Deborah Kurrasch. view more
Credit: Riley Brandt, University of Calgary
For more than a third of children living with epilepsy, the currently approved medications do not stop their seizures. This statistic has not changed for the past five decades, despite the development of many new anti-seizure drugs.
Deborah Kurrasch, PhD, a neuroscientist and Dr. Jong Rho, a pediatric neurologist at the Cumming School of Medicine (CSM), wondered about the reasons for the slow progress and started questioning the methods used to develop new medications.
"For many years, the focus has been on finding drugs that block channels and receptors in the brain that affect the way signals are made between cells. We wanted to find new drugs for the epileptic children who don't respond to current medications, and this required a wholly different approach," says Kurrasch, associate professor and member of the Alberta Children's Hospital Research Institute (ACHRI) and the Hotchkiss Brain Institute (HBI) at the CSM.
They started investigating the effectiveness of the ketogenic diet - a high fat, low carbohydrate diet that can reduce seizures in patients who are treatment-resistant. "The ketogenic diet is thought to work by changing the way cells produce energy, and for reasons that are not fully understood, this shift in energy production calms the excitability within epileptic brains," says Rho, professor and a member of ACHRI and the HBI. "We wondered if we could exploit this principle to find different drugs that help decrease seizure activity."
That led them to develop a new drug screening method that measures energy production in the background of a diseased brain. Specifically, they tested new drugs in zebrafish, a small, tropical fish genetically similar to humans whose brains can develop seizures in a manner similar to patients with epilepsy. Importantly, the researchers began testing drugs currently used for diseases other than epilepsy. Because these drugs are already approved and known to be safe, they can be rapidly translated into clinical use.
Using this approach, Kurrasch and Rho made a surprising discovery. "We tested a drug currently used for cancer treatment (vorinostat (Zolinza™)) and found that it reduced average daily seizures in zebrafish and mouse models by 60 per cent," says Kurrasch. This finding was recently published in Brain, a Journal of Neurology.
This spring, a clinical trial will start at the Alberta Children's Hospital exploring the clinical efficacy of vorinostat in children who have failed to respond to current anti-seizure medications.
"It's encouraging how quickly we can move from the lab to a potential treatment for patients," says Kurrasch. "This drug testing method that we've developed for epilepsy has so many more applications. We can now start looking at effective drug treatment for other disorders, including autism."
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Brain Canada invested $3 million toward this research program to develop the new drug-testing platform; in addition, ACHRI provided the matching dollars for this award from the support of community donations through the Alberta Children's Hospital Foundation. HBI - through their Translational Research Fund - is the primary sponsor of the vorinostat clinical trial, with supplementary funding from ACHRI.
Deborah Kurrasch, PhD, is an associate professor in the departments of Medical Genetics and Biochemistry & Molecular Biology and a member of the Alberta Children's Hospital Research Institute and the Hotchkiss Brain Institute at the CSM.
Dr. Jong Rho is a professor in the departments of Paediatrics, Physiology and Pharmacology, and Clinical Neurosciences, and a member of the Alberta Children's Hospital Research Institute and the Hotchkiss Brain Institute at the CSM.
Journal
Brain