Epilepsy is a brain disorder of abnormally increased brain excitability that leads to seizures. A person is considered to have epilepsy when he or she has two or more unprovoked seizures. Advances in therapeutics have improved the lives of patients with epilepsy, yet seizures refractory to medical intervention remain a significant cause of disability. Additionally, many of the patients who do achieve acceptable control of seizures with anti-epilepsy drugs suffer side-effects from multi-drug combinations or high dosages, and may still develop drug resistance. Surgical removal of seizure-producing areas of the brain can control seizures in some patients, but is less effective in others. Thus, although substantial strides have been made in treating epilepsy, new therapies are warranted to help the many patients who suffer intractable seizures or complications from medical or surgical treatment efforts. Dr. Dane M. Chetkovich is using his 2009 BRF Seed Grant to attempt to develop new epilepsy treatments to better the lives of these patients.
The abnormal brain excitability that causes seizures often results from genetic or acquired deficiencies in ion channels that control neuronal excitability. Ion channels are proteins that form a pore across the plasma membrane of cells. In neurons, these channels help regulate the electrical activity by controlling the flow of ions across the membrane. When the regulation is disrupted leading to a seizure, neurons may fire, or send signals on to other neurons in patterns that are very different from normal.
Dr. Chetkovich is focusing on a likely candidate for explaining abnormalities of excitability in both hereditary and acquired epilepsy—the hyperpolarization-activated cyclic nucleotide-gated (HCN) channel (h-channel). The h-channel family of ion channels consists of four different genes, HCN1-4, and has been implicated in epilepsy in animals and human patients. Dr. Chetkovich’s project will examine whether using engineered viruses to produce HCN2 in abnormal areas of epileptic brain can stop seizures. These experiments aim to develop and test techniques for viral gene therapy in an animal model of epilepsy with the ultimate goal of translating these techniques to patients with intractable epilepsy.
With his 2009 BRF Seed Grant, Dr. Dane M. Chetkovich generated enough data early on that allowed him to submit a grant proposal to NIH. In 2010, Dr. Chetkovich was awarded an R21 (an exploratory/developmental research grant provided by NIH) in the amount of $275,000.
The ultimate goal of Dr. Chetkovich’s research is to have his technique of gene therapy treatment for epilepsy get translated to patients that are otherwise resistant to medical and surgical therapy.

Other Grants

Sarah C. Goetz, Ph.D., Duke University
Uncovering a Novel Role for Primary Cilia in Eph/Ephrin Signaling in Neurons
2022 Seed GrantSarah C. Goetz, Ph.D. Duke University Women’s Council Seed Grant Primary cilia are tiny projections from cells that function like an antenna- they receive and may also send…
Erin M. Gibson, Ph.D., Stanford University
Circadian Regulation of Oligodendroglial Senescence and Metabolomics in Aging
2022 Seed GrantErin M. Gibson, Ph.D.Stanford University The brain consists of two main classes of cells, neurons and glia. Glia make-up more than half of the cells in the brain…
Yvette Fisher, Ph.D., University of California, Berkeley
Dynamic Modulation of Synaptic Plasticity During Spatial Exploration
2022 Seed GrantYvette Fisher, Ph.D.University of California, Berkeley The Virginia (Ginny) & Roger Carlson Seed Grant Cognitive flexibility is critical for appropriately adjusting thoughts and behaviors to meet changing demands…
Byoung Il Bae, Ph.D., University of Connecticut
Unique Vulnerability of Developing Human Cerebral Cortex to Loss of Centrosomal Protein
2022 Seed GrantByoung Il Bae, Ph.D.University of Connecticut Carl & Marilynn Thoma Foundation Seed Grant The cerebral cortex is the largest and outermost part of the human brain. It is…