Grant: Catalyst Grant: Musculoskeletal Health and Arthritis
University of Alberta
$99,300.00
Impaired Skeletal Muscle Pyruvate Dehydrogenase Activity & Chronic Fatigue Syndrome
EF 2016-17
Résumé
Chronic fatigue syndrome is a disorder characterized by severe fatigue and weakness of unknown origin, affecting anywhere from 2 to 25 of every 1000 individuals in the world today. The disorder affects severely impacts an individual's quality of life and productivity in the work force, and unfortunately has no specific treatments that target the root cause of the disorder, with current treatments aimed at improving its associated symptoms. Recent studies in humans have suggested that a reduced ability to burn carbohydrates/sugars for energy in skeletal muscle leads to muscle weakness and may be a key factor responsible for the severe fatigue in patients with chronic fatigue syndrome.
Of interest, we have a developed in our laboratory a genetically modified mouse model that has a reduced ability to burn carbohydrates/sugars for energy, and we have observed that these animals have reduced voluntary activity, which may be the result of early fatigue. Therefore, we would like to carry out detailed studies in our genetically modified mouse model to determine whether an impaired ability to burn carbohydrates/sugars in skeletal muscle for energy is indeed a root cause for chronic fatigue syndrome. We will address this by measuring exercise capacity in our animals (both forced and voluntary exercise). If our results prove true it will suggest that increasing carbohydrate/sugar metabolism in skeletal muscle might be an exciting new strategy to treat chronic fatigue syndrome by actually attacking a mechanism causing this disorder, versus our current treatments that simply deal with improving patient symptoms.
Programme
Catalyst Grant: Musculoskeletal Health and Arthritis
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
364136
Name
Ussher John R
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Planning and Dissemination Grants - ICS ME/CFS
Projecttitle
Impaired Skeletal Muscle Pyruvate Dehydrogenase Activity & Chronic Fatigue Syndrome
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$99,300
Cihrequipment2
$0
Programname2
Catalyst Grant: Musculoskeletal Health and Arthritis
Keyworddelim
Chronic Fatigue Syndrome; Energy Metabolism; Exercise; Glucose Oxidation; Lactate; Metabolomics; Mitochondrial Function; Pyruvate Dehydrogenase; Skeletal Muscle; Voluntary Activity
Abstract
Chronic fatigue syndrome is a disorder characterized by severe fatigue and weakness of unknown origin, affecting anywhere from 2 to 25 of every 1000 individuals in the world today. The disorder affects severely impacts an individual's quality of life and productivity in the work force, and unfortunately has no specific treatments that target the root cause of the disorder, with current treatments aimed at improving its associated symptoms. Recent studies in humans have suggested that a reduced ability to burn carbohydrates/sugars for energy in skeletal muscle leads to muscle weakness and may be a key factor responsible for the severe fatigue in patients with chronic fatigue syndrome.
Of interest, we have a developed in our laboratory a genetically modified mouse model that has a reduced ability to burn carbohydrates/sugars for energy, and we have observed that these animals have reduced voluntary activity, which may be the result of early fatigue. Therefore, we would like to carry out detailed studies in our genetically modified mouse model to determine whether an impaired ability to burn carbohydrates/sugars in skeletal muscle for energy is indeed a root cause for chronic fatigue syndrome. We will address this by measuring exercise capacity in our animals (both forced and voluntary exercise). If our results prove true it will suggest that increasing carbohydrate/sugar metabolism in skeletal muscle might be an exciting new strategy to treat chronic fatigue syndrome by actually attacking a mechanism causing this disorder, versus our current treatments that simply deal with improving patient symptoms.
Competitiondate
201701
Approvedterm2
1 yr 0 mth
Pinamesdelim
Ussher, John R
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $99,300~ $0~