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Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships

Queen's University (Kingston, Ontario)

$105,000.00

Enhancing motor recovery in a non-human primate model of chronic stroke by inhibiting pro-death neuronal signaling

FY 2017-18

Summary
Stroke is a disorder with staggering emotional and socioeconomic impact. It is a leading cause of death in Canada and leaves the majority of survivors with long-term disabilities that significantly diminish their autonomy and quality of life. Motor recovery following a stroke is critically dependent upon the survival of mature and newly born neurons in brain areas adjacent to the injury. In fact, the degree reallocation of motor function to adjacent areas has been shown to be related to the proficiency of motor recovery. Recovery can be hindered by the fact that in the days to weeks following a stroke, neurotoxic signaling resulting from physiological stress from the initial injury increases and can cause neuronal death. Classes of molecules that inhibit neurotoxic signaling pathways may have neuroprotective properties and promote pro-survival signaling. The drug NA-1 is one such inhibitor and its administration in the days following a stroke could promote neuronal survival and improve motor recovery. We will assess the motor function of Cynomolgus macaques using behavioral tests and determine baseline brain connectivity using functional imaging. The animals will undergo a transient medial cerebral artery occlusion to induce a stroke and will be given injections of either NA-1 or placebo during recovery. We will continuously assess motor function and brain connectivity throughout recovery to determine whether NA-1 can significantly improve neuronal survival, functional connectivity, and motor control. The findings of the proposed research has important implications for the efficacy of such drugs in improving stroke recovery which can lessen the socioeconomic burden and the emotional and physical strain of stroke related disabilities.
Program
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
383294
Name
Chen Yining
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Clinical
Prcname2
Doctoral Research Awards - A
Projecttitle
Enhancing motor recovery in a non-human primate model of chronic stroke by inhibiting pro-death neuronal signaling
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Fmri; Motor System; Recovery; Stroke
Abstract
Stroke is a disorder with staggering emotional and socioeconomic impact. It is a leading cause of death in Canada and leaves the majority of survivors with long-term disabilities that significantly diminish their autonomy and quality of life. Motor recovery following a stroke is critically dependent upon the survival of mature and newly born neurons in brain areas adjacent to the injury. In fact, the degree reallocation of motor function to adjacent areas has been shown to be related to the proficiency of motor recovery. Recovery can be hindered by the fact that in the days to weeks following a stroke, neurotoxic signaling resulting from physiological stress from the initial injury increases and can cause neuronal death. Classes of molecules that inhibit neurotoxic signaling pathways may have neuroprotective properties and promote pro-survival signaling. The drug NA-1 is one such inhibitor and its administration in the days following a stroke could promote neuronal survival and improve motor recovery. We will assess the motor function of Cynomolgus macaques using behavioral tests and determine baseline brain connectivity using functional imaging. The animals will undergo a transient medial cerebral artery occlusion to induce a stroke and will be given injections of either NA-1 or placebo during recovery. We will continuously assess motor function and brain connectivity throughout recovery to determine whether NA-1 can significantly improve neuronal survival, functional connectivity, and motor control. The findings of the proposed research has important implications for the efficacy of such drugs in improving stroke recovery which can lessen the socioeconomic burden and the emotional and physical strain of stroke related disabilities.
Competitiondate
201710
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Chen, Yining
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~