Grant: Project Grant
University of Calgary
$1,181,925.00
Mechanisms of suppression of excitotoxicity by endogenous amyloid beta
FY 2019-20
Summary
Stroke is a top 3 cause of death and the leading cause of disability in the developed world. Clinical treatments are quite effective at stopping strokes by using clot busting drugs or surgery to reopen blocked blood vessels. Despite these important advances, our understanding of how cell death mechanisms are intrinsically controlled is poor. This is surprising considering the overlap of the pathways for cell death and those for making memories. This proposal will address the cellular mechanisms of how one of the causative proteins in Alzheimer's disease modifies neuronal responses to stroke. We are particularly interested in how amyloid beta reduces loss of electrical activity in neurons, which is an important factor in neuronal death. Once complete, we will understand how stroke and amyloid interact and have a new foundation to investigate if stroke induces long-term changes in amyloid.
Department
Program
Project Grant
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
409508
Name
Thompson Roger J
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Systems & Circuits Neurosciences - A
Projecttitle
Mechanisms of suppression of excitotoxicity by endogenous amyloid beta
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$1,181,925
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Amyloid; Excitotoxicity; Pannexin; Stroke
Abstract
Stroke is a top 3 cause of death and the leading cause of disability in the developed world. Clinical treatments are quite effective at stopping strokes by using clot busting drugs or surgery to reopen blocked blood vessels. Despite these important advances, our understanding of how cell death mechanisms are intrinsically controlled is poor. This is surprising considering the overlap of the pathways for cell death and those for making memories. This proposal will address the cellular mechanisms of how one of the causative proteins in Alzheimer's disease modifies neuronal responses to stroke. We are particularly interested in how amyloid beta reduces loss of electrical activity in neurons, which is an important factor in neuronal death. Once complete, we will understand how stroke and amyloid interact and have a new foundation to investigate if stroke induces long-term changes in amyloid.
Competitiondate
201909
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Thompson, Roger J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,181,925~ $0~