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Grant: CIHR Fellowship

University of British Columbia

$135,000.00

Using optogenetics to identify and regulate cortical circuits that lead to interhemispheric inhibition after stroke

FY 2012-13

Summary
A stroke is caused by a rapid disruption in blood flow to a certain brain region, thus causing brain cells to die. The burden of this disease is significant. With 50,000 new cases occurring each year it is the leading cause of disability in Canada. One potential way for decreasing the impact of stroke is to develop treatment strategies that enhance the brain's inherent capacity to reorganize and recover some of the lost functions. Recent work suggests that transcranial magnetic brain stimulation (which can be applied non-invasively) can enhance the beneficial effects of rehabilitation by transiently reversing some of the brain abnormalities caused by the stroke. In the current experiments we will use a mouse model of stroke to further optimize brain stimulation parameters and also examine the mechanisms of action for effective brain stimulation. Our experiments will utilize a recently developed technology, which allows for light stimulation delivered to the brain to activate selective brain regions. Using this approach we will first identify the specific brain regions that enhance recovery when stimulated by light. In addition, we will also identify optimal stimulation parameters, such as the timing and duration of stimulation. Lastly, we will evaluate the effects of modulating a specific sub-population of neurons within the brain. This population of cells normally sends out inhibitory messages, acting to keep brain activity in check. A stroke may induce over-activity in these cells, thus producing too much inhibition. We will examine the effects of inhibiting these overactive cells with the hope of improving brain function after a stroke.
Program
CIHR Fellowship
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
281957
Name
Silasi Gergely
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Using optogenetics to identify and regulate cortical circuits that lead to interhemispheric inhibition after stroke
Programtype2
Fellowship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$135,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Behaviour; Chronic Window; Interhemispheric Inhibition; Motor Cortex; Motor Mapping; Optogenetics; Plasticity; Recovery; Stroke; Transcranial Magnetic Stimulation
Abstract
A stroke is caused by a rapid disruption in blood flow to a certain brain region, thus causing brain cells to die. The burden of this disease is significant. With 50,000 new cases occurring each year it is the leading cause of disability in Canada. One potential way for decreasing the impact of stroke is to develop treatment strategies that enhance the brain's inherent capacity to reorganize and recover some of the lost functions. Recent work suggests that transcranial magnetic brain stimulation (which can be applied non-invasively) can enhance the beneficial effects of rehabilitation by transiently reversing some of the brain abnormalities caused by the stroke. In the current experiments we will use a mouse model of stroke to further optimize brain stimulation parameters and also examine the mechanisms of action for effective brain stimulation. Our experiments will utilize a recently developed technology, which allows for light stimulation delivered to the brain to activate selective brain regions. Using this approach we will first identify the specific brain regions that enhance recovery when stimulated by light. In addition, we will also identify optimal stimulation parameters, such as the timing and duration of stimulation. Lastly, we will evaluate the effects of modulating a specific sub-population of neurons within the brain. This population of cells normally sends out inhibitory messages, acting to keep brain activity in check. A stroke may induce over-activity in these cells, thus producing too much inhibition. We will examine the effects of inhibiting these overactive cells with the hope of improving brain function after a stroke.
Competitiondate
201302
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Silasi, Gergely
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $135,000~ $0~