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Grant: Project Grant

McGill University

$745,876.00

AIP-Trap to prevent amyloid neurotoxicity in Alzheimer disease-relevant mouse models

EF 2019-20

Résumé
Alzheimer disease (AD) is the most prevalent neurodegenerative disorder in the world, estimated to currently affect over 35 million people globally. As the life expectancy continues to increase, the number of Canadians suffering from this debilitating, adult-onset disease (2011: 747,000 affected with $33B health care costs) is expected to double by 2040 (over 1.4M affected, $293B health care costs). In part, AD neurodegeneration is caused by a specific peptide (amyloid-beta (Abeta)) that forms toxic aggregates in the brain. Recently, we have identified an Abeta-oligomer Interacting Peptide (AIP) that provides beneficial effects by decreasing Abeta neurotoxicity. In this proposal, we will test a novel, next generation AIP molecule to (i) advance our understanding of the molecular processes leading to amyloid plaque formation in the brain, and (ii) explore the consequences of our novel approach to inhibit neurotoxicity of Abeta.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
420482
Name
Multhaup Gerhard
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Systems & Circuits Neurosciences - A
Projecttitle
AIP-Trap to prevent amyloid neurotoxicity in Alzheimer disease-relevant mouse models
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$745,876
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Aggregation; Alzheimer'S Disease; Animal Models; Drug And Pharmacological Approaches; Molecular And Cellular Mechanisms; Neurodegeneration; Protein Misfolding
Abstract
Alzheimer disease (AD) is the most prevalent neurodegenerative disorder in the world, estimated to currently affect over 35 million people globally. As the life expectancy continues to increase, the number of Canadians suffering from this debilitating, adult-onset disease (2011: 747,000 affected with $33B health care costs) is expected to double by 2040 (over 1.4M affected, $293B health care costs). In part, AD neurodegeneration is caused by a specific peptide (amyloid-beta (Abeta)) that forms toxic aggregates in the brain. Recently, we have identified an Abeta-oligomer Interacting Peptide (AIP) that provides beneficial effects by decreasing Abeta neurotoxicity. In this proposal, we will test a novel, next generation AIP molecule to (i) advance our understanding of the molecular processes leading to amyloid plaque formation in the brain, and (ii) explore the consequences of our novel approach to inhibit neurotoxicity of Abeta.
Competitiondate
202003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Multhaup, Gerhard
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $745,876~ $0~