Grant: Environments, Genes and Chronic Disease
McMaster University
$1,998,323.00
Gene Environment Team on Brown/beige Adipose Tissue (GET_BAT)
EF 2015-16
Résumé
More than 5 million Canadians have the chronic interrelated diseases of obesity, non-alcoholic fatty liver disease (NAFLD) and type 2 diabetes (T2D) and their incidence in the population are rapidly increasing. Obesity is an important risk factor for developing NAFLD and T2D which contribute to the development of liver cancer and heart disease. Therefore, designing new ways to treat or prevent T2D and NAFLD are important. Brown adipose tissue (BAT) is an organ which has long been known to exist in rodents and infants but remarkably only in the last 5 years has been discovered in adult humans. BAT has the unique capability, compared to any other organ in the body, to burn large amounts of sugar and fat and effectively dissipate this energy as heat due to the presence of unique protein called uncoupling protein 1. Thus BAT is frequently characterized as the body's furnace. The activation of BAT in rodents has been shown to reverse obesity, T2D and NAFLD. In addition recent studies have shown that by exposing humans to cold you can increase BAT activity and lower blood sugar levels suggesting that increasing BAT activity may represent a viable therapy for treating T2D. Unfortunately, in individuals with obesity or T2D the ability to switch on BAT is compromised. Determining why BAT activity is reduced and identifying new ways to switch it on has generated world-wide scientific and clinical excitement around developing a new therapy for obesity, NAFLD and T2D and is the focus of the current proposal. In this proposal we will conduct studies in cells, mice and humans to examine how agricultural and food processing practices may regulate BAT metabolic activity directly or indirectly by altering the billions of bacteria that reside within our gastrointestinal tract. These studies will help us develop new strategies to enhance BAT activity that may be effective for treating and preventing obesity, NAFLD and T2D.
Programme
Environments, Genes and Chronic Disease
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
335182
Name
Steinberg Gregory R
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Other: Programmatic Grants in Environments, Genes and Chronic Disease
Projecttitle
Gene Environment Team on Brown/beige Adipose Tissue (GET_BAT)
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$1,998,323
Cihrequipment2
$0
Programname2
Environments, Genes and Chronic Disease
Keyworddelim
Brown Adipose Tissue; Children; Elderly; Herbicides; High Fructose Corn Syrup; Non-Alcoholic Fatty Liver Disease (Nafld); Obesity; Pesticides; Serotonin; Type 2 Diabetes
Abstract
More than 5 million Canadians have the chronic interrelated diseases of obesity, non-alcoholic fatty liver disease (NAFLD) and type 2 diabetes (T2D) and their incidence in the population are rapidly increasing. Obesity is an important risk factor for developing NAFLD and T2D which contribute to the development of liver cancer and heart disease. Therefore, designing new ways to treat or prevent T2D and NAFLD are important. Brown adipose tissue (BAT) is an organ which has long been known to exist in rodents and infants but remarkably only in the last 5 years has been discovered in adult humans. BAT has the unique capability, compared to any other organ in the body, to burn large amounts of sugar and fat and effectively dissipate this energy as heat due to the presence of unique protein called uncoupling protein 1. Thus BAT is frequently characterized as the body's furnace. The activation of BAT in rodents has been shown to reverse obesity, T2D and NAFLD. In addition recent studies have shown that by exposing humans to cold you can increase BAT activity and lower blood sugar levels suggesting that increasing BAT activity may represent a viable therapy for treating T2D. Unfortunately, in individuals with obesity or T2D the ability to switch on BAT is compromised. Determining why BAT activity is reduced and identifying new ways to switch it on has generated world-wide scientific and clinical excitement around developing a new therapy for obesity, NAFLD and T2D and is the focus of the current proposal. In this proposal we will conduct studies in cells, mice and humans to examine how agricultural and food processing practices may regulate BAT metabolic activity directly or indirectly by altering the billions of bacteria that reside within our gastrointestinal tract. These studies will help us develop new strategies to enhance BAT activity that may be effective for treating and preventing obesity, NAFLD and T2D.
Competitiondate
201509
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Steinberg, Gregory R; Morrison, Katherine M
Approvedterm
5 ans 0 mois
Cihrcontribution2
Inst of Nutr Metabolism &Diab~ $731,010~ $0~Major Initiatives #3~ $1,267,313~ $0~