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Grant: Operating Grant

University of Ottawa

$779,350.00

Tubular dysfunction in diabetes: role of PGE2/EP receptors

EF 2011-12

Résumé
Diabetic nephropathy (DN) is a leading cause of chronic kidney disease, and is recognized as one of the more important causes of morbidity and mortality in Canada. In the kidney, prostaglandins are implicated in the maintenance of glomerular filtration, they regulate cell growth and death responses, affect vascular integrity, and transport of water and electrolytes (sodium, potassium) along the tubules. DN involves disturbances in all these aspects of kidney function, therefore prostaglandins may be targeted to help slow the progression of these changes in the kidney. Though we have long recognized the involvement of prostaglandins in DN, to this day we are unsure of their exact contribution, whether they propagate the renal changes or serve to counteract the harmful effects of other agents. Prostaglandins are mainly produced in the glomeruli and collecting ducts of the kidney, by proteins called cyclooxygenases, which are inhibited by non-steroidal anti-inflammatory drugs (NSAIDs). Diabetes is an epidemic in North America and accounts for 30% of patients with chronic kidney disease. We strongly believe this research can lead to novel targets for the treatment of diabetic kidney disease and improve the lives of those affected.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
238050
Name
Hébert Richard L
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Hematology, Digestive Disease & Kidney
Projecttitle
Tubular dysfunction in diabetes: role of PGE2/EP receptors
Programtype2
Operating Grants
Orgnameinp2
University of Ottawa
Cihramount2
$779,350
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Apoptosis; Cell Growth; Diabetic Nephropathy; Ep1 Knockout Mouse; Fibrosis; Fvb And Diabetic (Ove-26) Mouse Model; Isolated Perfused Mouse Cortical Collecting Duct; Isolated Perfused Mouse Proximal Tubules; Sodium Transport; Water Flow
Abstract
Diabetic nephropathy (DN) is a leading cause of chronic kidney disease, and is recognized as one of the more important causes of morbidity and mortality in Canada. In the kidney, prostaglandins are implicated in the maintenance of glomerular filtration, they regulate cell growth and death responses, affect vascular integrity, and transport of water and electrolytes (sodium, potassium) along the tubules. DN involves disturbances in all these aspects of kidney function, therefore prostaglandins may be targeted to help slow the progression of these changes in the kidney. Though we have long recognized the involvement of prostaglandins in DN, to this day we are unsure of their exact contribution, whether they propagate the renal changes or serve to counteract the harmful effects of other agents. Prostaglandins are mainly produced in the glomeruli and collecting ducts of the kidney, by proteins called cyclooxygenases, which are inhibited by non-steroidal anti-inflammatory drugs (NSAIDs). Diabetes is an epidemic in North America and accounts for 30% of patients with chronic kidney disease. We strongly believe this research can lead to novel targets for the treatment of diabetic kidney disease and improve the lives of those affected.
Competitiondate
201109
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Hébert, Richard L
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $779,350~ $0~