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Grant: CIHR Fellowship

Direct Payment

$150,000.00

Effects of diet-induced obesity on anhedonia: a focus on translationally relevant endpoints.

EF 2023-24

Résumé
Diet induced obesity, and corresponding metabolic dysfunction (ie. type 2 diabetes) is a major health issue for many Canadians, but we continue to lack long-term effective treatments. Many individuals who are obese have co-morbid conditions including depression. One of the most commonly reported manifestations of depression is altered sleep patterns, including too much or too little sleep, as well as altered food reward seeking. Here I will investigate how diet induced obesity alters sleep and reward in a mouse model. Furthermore, I will look at how different genetic profiles may be driving these behaviours. A key feature of this proposal is the use of behavioral and genetic endpoints that are defined, collected, and analyzed in the same ways in rodents as in humans. This will provide novel gene targets for the treatment of depression in individuals who are obese, a mood disorder with historically ineffective treatments in the obese population.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
Massachusetts, United States of America
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
492627
Name
Seabrook Lauren
Region
Massachusetts
Country
United States of America
Orgtype
Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Effects of diet-induced obesity on anhedonia: a focus on translationally relevant endpoints.
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Anhedonia; Animal Behaviour; Inflammation; Neuroscience; Reward Reactivity; Sleep
Abstract
Diet induced obesity, and corresponding metabolic dysfunction (ie. type 2 diabetes) is a major health issue for many Canadians, but we continue to lack long-term effective treatments. Many individuals who are obese have co-morbid conditions including depression. One of the most commonly reported manifestations of depression is altered sleep patterns, including too much or too little sleep, as well as altered food reward seeking. Here I will investigate how diet induced obesity alters sleep and reward in a mouse model. Furthermore, I will look at how different genetic profiles may be driving these behaviours. A key feature of this proposal is the use of behavioral and genetic endpoints that are defined, collected, and analyzed in the same ways in rodents as in humans. This will provide novel gene targets for the treatment of depression in individuals who are obese, a mood disorder with historically ineffective treatments in the obese population.
Competitiondate
202310
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Seabrook, Lauren
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~