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Grant: Project Grant

McGill University

$1,189,576.00

How exercise improves ataxia in SCA6

FY 2022-23

Summary
Spinocerebellar ataxia type 6 (SCA6) is a devastating genetic disease that leads to progressive motor impairment (called ataxia) and cerebellar degeneration. SCA6 currently has no known treatment. Using a mouse model of SCA6, we found that exercise could improve ataxia and have identified some of the cellular changes in the cerebellum that we believe underlie the effects of exercise, since rescuing these cellular changes led to reduced ataxia. Here, we aim to unravel the mechanisms that underlie the improvements in ataxia by exercise or a drug that mimics it in SCA6 mice in the hope that this may lead to new, more specific treatment avenues in the future. This work will result in important findings that could contribute to new treatments for a currently untreatable disease.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
479005
Name
Watt Alanna
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Movement & Exercise
Projecttitle
How exercise improves ataxia in SCA6
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$1,189,576
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Ataxia; Behaviour; Cerebellum; Exercise; Motor System; Signaling Pathway
Abstract
Spinocerebellar ataxia type 6 (SCA6) is a devastating genetic disease that leads to progressive motor impairment (called ataxia) and cerebellar degeneration. SCA6 currently has no known treatment. Using a mouse model of SCA6, we found that exercise could improve ataxia and have identified some of the cellular changes in the cerebellum that we believe underlie the effects of exercise, since rescuing these cellular changes led to reduced ataxia. Here, we aim to unravel the mechanisms that underlie the improvements in ataxia by exercise or a drug that mimics it in SCA6 mice in the hope that this may lead to new, more specific treatment avenues in the future. This work will result in important findings that could contribute to new treatments for a currently untreatable disease.
Competitiondate
202303
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Watt, Alanna
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,189,576~ $0~