Grant: Project Grant
University of Calgary
$1,147,500.00
Unraveling early pathological mechanisms of Alzheimer's disease to develop interventions
EF 2025-26
Résumé
Alzheimer's disease (AD) is the most common form of dementia, affecting millions of people and placing a significant burden on healthcare. Research suggests that early intervention before memory loss could be the key to slowing disease progression. Our study focuses on one of the earliest affected brain regions, the dorsal raphe nucleus (DRN) which contains serotonin cells. These cells play a crucial role in emotional and social function, which are impaired early in disease course. We have developed a mouse model that mimics these changes observed in the initial stages of AD, including abnormal buildup of a protein called tau in DRN serotonin neurons and the appearance of behavioural impairments. Our research
will explore how tau disrupts function of these cells and the regions they connect with, resulting in the early symptoms of AD. Using cutting-edge imaging, molecular and behavioural techniques in our mouse model, we aim to uncover these changes and test potential treatments to prevent disease progression. By identifying the early changes that disrupt brain function and testing ways to counteract them, our work could help develop new treatments and improve the quality of life for those at risk.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
533278
Name
Sargin Derya
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Systems & Circuits Neurosciences - A
Projecttitle
Unraveling early pathological mechanisms of Alzheimer's disease to develop interventions
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$1,147,500
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Alzheimer'S Disease; Dorsal Raphe Nucleus; Mouse Models; Neuropsychiatric Symptoms; Serotonin; Tau
Abstract
Alzheimer's disease (AD) is the most common form of dementia, affecting millions of people and placing a significant burden on healthcare. Research suggests that early intervention before memory loss could be the key to slowing disease progression. Our study focuses on one of the earliest affected brain regions, the dorsal raphe nucleus (DRN) which contains serotonin cells. These cells play a crucial role in emotional and social function, which are impaired early in disease course. We have developed a mouse model that mimics these changes observed in the initial stages of AD, including abnormal buildup of a protein called tau in DRN serotonin neurons and the appearance of behavioural impairments. Our research
will explore how tau disrupts function of these cells and the regions they connect with, resulting in the early symptoms of AD. Using cutting-edge imaging, molecular and behavioural techniques in our mouse model, we aim to uncover these changes and test potential treatments to prevent disease progression. By identifying the early changes that disrupt brain function and testing ways to counteract them, our work could help develop new treatments and improve the quality of life for those at risk.
Competitiondate
202509
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Sargin, Derya
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,147,500~ $0~