Controlling epilepsy symptoms with precisely timed inhibition and circuit editing
Active Project Grant Awarded Last action
- Award ID
- F32NS146143
- Recipient
-
Icahn School Of Medicine At Mount Sinai UEI C8H9CNG1VBD9
- Awarding agency
-
National Institute of Neurological Disorders and Stroke
National Institutes of Health, Department of Health and Human Services
- Obligated
- $150,512
Award facts
- Assistance listing
- 93.853 Extramural Research Programs in the Neurosciences and Neurological Disorders
- Completion date 9% complete
- Originally
- Place of performance
- New York, NY 10029, USA
Award details come from USAspending.gov.
About this award
The National Institute of Neurological Disorders and Stroke awarded Icahn School of Medicine at Mount Sinai $150,512 on August 5, 2026, under the Extramural Research Programs in the Neurosciences and Neurological Disorders program (CFDA 93.853).
The award funds research into controlling epilepsy symptoms through precisely timed inhibition and circuit editing, focused on temporal lobe epilepsy and cognitive impairments associated with seizure disorders. The research employs closed-loop optogenetic stimulation to restore proper spike timing of dentate gyrus interneurons in the hippocampus, with the hypothesis that restoring this timing will reduce seizure susceptibility and restore learning and memory deficits in epilepsy models. The work includes two aims: testing whether altering or restoring dentate gyrus interneuron spike timing relative to ongoing theta oscillations affects learning and memory behavior in both non-epileptic and epileptic mice, and employing a novel circuit-editing tool to increase connectivity as an alternative to optogenetic approaches with greater translational potential.
Work is performed in New York, New York, with a period of performance extending from August 5, 2026, through March 4, 2029. The award is classified as a Project Grant.
Description
- Abstract
- Temporal lobe epilepsy (TLE) is a complex neurological disorder that is characterized by spontaneous, reoccurring seizures and often presents with debilitating cognitive comorbidities including learning and memory deficits. Current treatments for TLE are ineffective at managing cognitive comorbidities and often exacerbate these symptoms. The mechanisms underlying cognitive impairments in TLE are poorly understood, but learning and memory deficits are thought to arise when TLE pathologies disrupt the normal function of hippocampal circuits that support these cognitive processes. Circuits in the hippocampal dentate gyrus (DG) are known to support learning and memory and have been shown to be disrupted in TLE patients and in animal models of TLE. Recently, DR. Shuman showed that the spike timing of DG interneurons is disrupted in TLE. Additionally, he showed that restoring proper spike timing of DG interneurons with closed-loop optogenetic stimulation decreased seizure susceptibility in TLE mice. Because proper spike timing in the hippocampus is an important mechanism that supports learning and memory computations, i hypothesize that DG interneuron spike timing is also important for behavior. In aim 1, i will test this hypothesis by using closed- loop optogenetic stimulation to alter the spike timing of DG interneurons relative to ongoing theta oscillations. I predict that disrupting DG interneuron spike timing in non-epileptic mice will impair learning and memory while restoring the disrupted spike timing of DG interneurons in TLE mice will restore learning and memory deficits. While optogenetic approaches are great for assessing the causal relationships between physiological processes and behavior, there are a number of barriers that limit the translational potential of optogenetics. In aim 2, i will employ a novel circuit-editing tool to increase connectivity between DG interneurons and their upstream inputs in the medial entorhinal cortex (MEC) with the goal of increasing feedforward inhibition in the DG. I hypothesize that increasing connectivity to DG interneurons will decrease seizure susceptibility. Additionally, i predict that this approach will restore the proper spike timing of DG interneurons because inputs fire at the same preferred phase of theta as DG interneurons and are not disrupted in TLE. Circuit-editing is a novel technique that has never been applied to epilepsy. Successful implementation of this approach could result in a transformative gene therapy for epilepsy patients and will inform how feedforward inhibition in the DG normally supports hippocampal physiology. The following research project and training plan were designed to help me grow both scientifically and professionally, and support from this grant will be invaluable as i continue to work towards my goal of becoming an independent researcher. The outstanding opportunities provided by the shuman lab and mount sinai provide the ideal training environment for me as i pursue my postdoctoral fellowship and ultimately a career in academic research.
Transactions
| Action | Obligated | Date |
|---|---|---|
| Amendment | $1,248 | |
| Amendment | $74,632 | |
| Amendment | $0 | |
| Original award | $74,632 |
Quick answers
Who received award F32NS146143?
F32NS146143 was awarded to Icahn School Of Medicine At Mount Sinai by National Institute of Neurological Disorders and Stroke (National Institutes of Health) on August 5, 2026.
How much is award F32NS146143 worth?
$150,512 has been obligated on F32NS146143.
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