Grant: Operating Grant
University of Toronto
$774,325.00
Novel mediators of beta-cell lipotoxicity
EF 2012-13
Résumé
Obesity affects more than 25% of Canadians and is a major risk factor for type 2 diabetes, which affects more than 6% of Canadians. Both obesity and diabetes are major and increasing causes of morbidity and mortality. Recently, inflammation of the pancreatic islets has been found in type 2 diabetic patients. Elevated levels of fatty acids in the circulation (fatty acids are released from the adipose tissue) are often present in obesity, and may lead to type 2 diabetes in predisposed individuals by causing inflammation of the pancreatic beta cell which secretes insulin. The objective of this proposal is to investigate how elevated fatty acids lead to inflammation of the pancreatic islets that causes beta cell malfunction. More specifically, we will identify the receptors and signaling molecules involved and whether fat also reduces the antinflammatory defenses. These studies are important to identify targets to prevent and treat malfunction of beta cells during the development of diabetes and during the progression of beta cell failure in type 2 diabetes.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
266427
Name
Giacca Adria
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders
Projecttitle
Novel mediators of beta-cell lipotoxicity
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$774,325
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Beta Cell; Diabetes; Free Fatty Acids; Hyperglycemic Clamp; In Vivo; Inflammation; Lipotoxicity; Obesity; Oxidative Stress; Sirtuins
Abstract
Obesity affects more than 25% of Canadians and is a major risk factor for type 2 diabetes, which affects more than 6% of Canadians. Both obesity and diabetes are major and increasing causes of morbidity and mortality. Recently, inflammation of the pancreatic islets has been found in type 2 diabetic patients. Elevated levels of fatty acids in the circulation (fatty acids are released from the adipose tissue) are often present in obesity, and may lead to type 2 diabetes in predisposed individuals by causing inflammation of the pancreatic beta cell which secretes insulin. The objective of this proposal is to investigate how elevated fatty acids lead to inflammation of the pancreatic islets that causes beta cell malfunction. More specifically, we will identify the receptors and signaling molecules involved and whether fat also reduces the antinflammatory defenses. These studies are important to identify targets to prevent and treat malfunction of beta cells during the development of diabetes and during the progression of beta cell failure in type 2 diabetes.
Competitiondate
201209
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Giacca, Adria
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $774,325~ $0~