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Grant: Operating Grant

University of British Columbia

$847,790.00

Npas4 Regulation of Glucose Homeostasis

EF 2014-15

Résumé
The brain and pancreas cooperate to regulate blood glucose levels both during the fasted state and following a meal. During the development of obesity and type 2 diabetes, glucose responsive cells in the brain and pancreas become dysfunctional which often worsens disease. We have a discovered a protein (Npas4) that is made in the pancreas and brain in response to glucose in normal people but not those with diabetes. We know that loss of this protein in mice causes them to eat more and causes their glucose levels to rise. However, we do not know exactly where in the brain it is acting; how in the pancreas it is acting; whether increased levels of this protein might be therapeutically beneficial or which other proteins Npas4 normally controls in either tissue. This proposal aims to answer these four questions as this could help us design new therapies that could be used to combat both obesity and diabetes.
Programme
Operating Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
323017
Name
Lynn Francis C
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders 2
Projecttitle
Npas4 Regulation of Glucose Homeostasis
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$847,790
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Bhlh-Pas; Endoplasmic Reticulum Stress; Gene Transcription; Glucolipodysfunction; Impaired Glucose Tolerance; Insulin Gene Expression; Insulin Secretion; Obesity; Type 2 Diabetes; ß-Cell Biology
Abstract
The brain and pancreas cooperate to regulate blood glucose levels both during the fasted state and following a meal. During the development of obesity and type 2 diabetes, glucose responsive cells in the brain and pancreas become dysfunctional which often worsens disease. We have a discovered a protein (Npas4) that is made in the pancreas and brain in response to glucose in normal people but not those with diabetes. We know that loss of this protein in mice causes them to eat more and causes their glucose levels to rise. However, we do not know exactly where in the brain it is acting; how in the pancreas it is acting; whether increased levels of this protein might be therapeutically beneficial or which other proteins Npas4 normally controls in either tissue. This proposal aims to answer these four questions as this could help us design new therapies that could be used to combat both obesity and diabetes.
Competitiondate
201503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Lynn, Francis C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $847,790~ $0~