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Grant: Operating Grant

Université Laval

$315,501.00

Glucagon-like peptide-1 and pancreatic beta-cell neogenesis

FY 2009-10

Summary
Diabetes mellitus, a metabolic disorder often associated with obesity, affects more than 2 million Canadians and 190 million people worldwide. The increased prevalence of diabetes constitutes a significant socio-economic problem. Thus, there is great need for new treatments. Insulin is produced in the pancreas by specialized cells, the beta-cells. Beta-cells play a central role in the development of diabetes. Type 1 diabetes results from selective destruction of beta-cells, whereas type 2 diabetes arises from a progressive deterioration of beta-cell mass and function. Thus, the reduction in the number of beta-cells is a common feature of both type 1 and type 2 diabetes. The ability to stimulate beta-cell regeneration could be a novel approach in the treatment of diabetes. Glucagon-like peptide 1 (GLP-1) is a promising drug in the treatment of diabetes. It's long-acting analog is commercialized under the name Byetta. A growing body of evidence suggests that GLP-1 could promote the formation of new beta-cells in the pancreas. The formation of new beta-cells is termed "beta-cell neogenesis". In this proposal, we seek to demonstrate that GLP-1 promotes beta-cell neogenesis and to identify the molecular mechanisms involved in the process.
Program
Operating Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
189316
Name
Buteau Jean
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders
Projecttitle
Glucagon-like peptide-1 and pancreatic beta-cell neogenesis
Programtype2
Operating Grants
Orgnameinp2
Université Laval
Cihramount2
$315,501
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Diabetes; Differentiation; Growth Factor; Pancreatic Beta-Cell; Proliferation; Signal Transduction
Abstract
Diabetes mellitus, a metabolic disorder often associated with obesity, affects more than 2 million Canadians and 190 million people worldwide. The increased prevalence of diabetes constitutes a significant socio-economic problem. Thus, there is great need for new treatments. Insulin is produced in the pancreas by specialized cells, the beta-cells. Beta-cells play a central role in the development of diabetes. Type 1 diabetes results from selective destruction of beta-cells, whereas type 2 diabetes arises from a progressive deterioration of beta-cell mass and function. Thus, the reduction in the number of beta-cells is a common feature of both type 1 and type 2 diabetes. The ability to stimulate beta-cell regeneration could be a novel approach in the treatment of diabetes. Glucagon-like peptide 1 (GLP-1) is a promising drug in the treatment of diabetes. It's long-acting analog is commercialized under the name Byetta. A growing body of evidence suggests that GLP-1 could promote the formation of new beta-cells in the pancreas. The formation of new beta-cells is termed "beta-cell neogenesis". In this proposal, we seek to demonstrate that GLP-1 promotes beta-cell neogenesis and to identify the molecular mechanisms involved in the process.
Competitiondate
200909
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Buteau, Jean
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $315,501~ $0~