Grant: Operating Grant
University of British Columbia
$947,283.00
Probing the circuits responsible for stroke recovery with light-mediated circuit monitoring and manipulation in mouse models.
EF 2010-11
Résumé
Reductions in blood flow to the brain of sufficient duration and extent lead to stroke, which results in damage to neuronal networks and impairment of sensation, movement, or cognition. Although stroke damage can be devastating, many patients survive the initial event and undergo some spontaneous recovery which that can be further augmented by rehabilitative therapy. It becoming clear that the ability of patients to recover is in part mediated by the ability of the brain circuits to adapt in a process called plasticity. My lab will apply new light-based techniques to address how the brain's sensory and motor circuits adapt in response to stroke. The brain is organized much like a circuit diagram within a computer with discrete wires or connections. However, none of the brain circuits or cells have color-coding or labels which enable technicians to service them. Here, using new genetic technologies we will employ strategies, which label select mouse neurons with fluorescent proteins, which enable them to glow under particular wavelengths of light. Not only can the glowing neurons be found by light, but they can also be controlled by light using new light-sensitive protein ion channels, which transmit light energy into excitation or inhibition. Using these fluorescing neurons, which can be controlled by light, we plan to unravel how the brains sensory and motor system adapt following damage due to stroke. We hope that by understanding how the brain can partially cope with stroke damage that this knowledge can be exploited to help patients through innovative brain stimulation or rehabilitative strategies. We have now devised new strategies for both exciting and inhibiting the brains of mouse models of stroke damage to aid these studies. Overall, our goal is that through insight into natural sensory and motor system adaptation novel treatments will ensue, permitting better lives for those affected by diseases such as stroke.
Programme
Operating Grant
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
210064
Name
Murphy Timothy H
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Systems & Circuits Neurosciences - A
Projecttitle
Probing the circuits responsible for stroke recovery with light-mediated circuit monitoring and manipulation in mouse models.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$947,283
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
2-Photon Imaging; Calcium; Channelrhodopsin-2; Dendrite; Optogenetics; Plasticity; Stroke; Synapse
Abstract
Reductions in blood flow to the brain of sufficient duration and extent lead to stroke, which results in damage to neuronal networks and impairment of sensation, movement, or cognition. Although stroke damage can be devastating, many patients survive the initial event and undergo some spontaneous recovery which that can be further augmented by rehabilitative therapy. It becoming clear that the ability of patients to recover is in part mediated by the ability of the brain circuits to adapt in a process called plasticity. My lab will apply new light-based techniques to address how the brain's sensory and motor circuits adapt in response to stroke. The brain is organized much like a circuit diagram within a computer with discrete wires or connections. However, none of the brain circuits or cells have color-coding or labels which enable technicians to service them. Here, using new genetic technologies we will employ strategies, which label select mouse neurons with fluorescent proteins, which enable them to glow under particular wavelengths of light. Not only can the glowing neurons be found by light, but they can also be controlled by light using new light-sensitive protein ion channels, which transmit light energy into excitation or inhibition. Using these fluorescing neurons, which can be controlled by light, we plan to unravel how the brains sensory and motor system adapt following damage due to stroke. We hope that by understanding how the brain can partially cope with stroke damage that this knowledge can be exploited to help patients through innovative brain stimulation or rehabilitative strategies. We have now devised new strategies for both exciting and inhibiting the brains of mouse models of stroke damage to aid these studies. Overall, our goal is that through insight into natural sensory and motor system adaptation novel treatments will ensue, permitting better lives for those affected by diseases such as stroke.
Competitiondate
201009
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Murphy, Timothy H
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $947,283~ $0~