Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Collaborative Health Research Projects

University of Western Ontario

$66,640.00

Development of GLP-1 receptor probes for imaging changes in beta cell mass

EF 2010-11

Résumé
Can we detect changes in beta cell mass in vivo? The answer to the question is comprised of three steps: 1) identifying a suitable probe that can selectively target the beta cell; 2) engineering the probe to carry an imaging isotope or contrast agent; and 3) selecting an imaging modality that has the appropriate sensitivity to detect small changes in beta cell number. In order to advance our understanding of the changes in beta cell mass before the onset of diabetes and during the progression of Type 2 diabetes, there is a critical need for imaging probes that can detect beta cells in the living animal. This proposal will focus on the development of novel radiolabelled probes for imaging using SPECT (single photon emission computed tomography) and PET (positron emission tomography) that can bind to GLP-1 receptors on the beta cell. The long-term outcome of these studies will be the discovery of a probe that can be used to detect changes in beta cell mass in vivo before the onset of diabetes, during the course of the disease and during regenerative therapy. This is of significant clinical value as it would be a predictive tool for changes in beta cell mass including non-invasive evaluation o therapy. This tool would also permit detection of islet transplantation and could follow the progressive decline in function of the islets thereby determining when intervention is required.
Programme
Collaborative Health Research Projects
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
351274-2008
Name nom
Luyt, Leonard
Department département
Chemistry
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2010
Competition year année de concours
2008
Award amount
66640
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
1101
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Human health (including medically-related psychological research)
Area of application fr
Santé publique (y compris recherche psychologique liée à la médecine)
Research subject code
3705
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Bio-organic chemistry
Research subject fr
Chimie bio-organique
Partie
3
Nb partie
3
Application title
Development of GLP-1 receptor probes for imaging changes in beta cell mass
Keyword
NSERC
Application summary
Can we detect changes in beta cell mass in vivo? The answer to the question is comprised of three steps: 1) identifying a suitable probe that can selectively target the beta cell; 2) engineering the probe to carry an imaging isotope or contrast agent; and 3) selecting an imaging modality that has the appropriate sensitivity to detect small changes in beta cell number. In order to advance our understanding of the changes in beta cell mass before the onset of diabetes and during the progression of Type 2 diabetes, there is a critical need for imaging probes that can detect beta cells in the living animal. This proposal will focus on the development of novel radiolabelled probes for imaging using SPECT (single photon emission computed tomography) and PET (positron emission tomography) that can bind to GLP-1 receptors on the beta cell. The long-term outcome of these studies will be the discovery of a probe that can be used to detect changes in beta cell mass in vivo before the onset of diabetes, during the course of the disease and during regenerative therapy. This is of significant clinical value as it would be a predictive tool for changes in beta cell mass including non-invasive evaluation o therapy. This tool would also permit detection of islet transplantation and could follow the progressive decline in function of the islets thereby determining when intervention is required.