Grant: Master's Award: Canada Graduate Scholarships
University of Northern British Columbia
$17,500.00
Targeted delivery of rosiglitazone to subcutaneous adipose tissue for the treatment of type 2 diabetes
EF 2023-24
Résumé
Obesity affects millions of Canadians, increasing the risk for many chronic diseases including type 2 diabetes. Fat, or adipose tissue, plays an important role in maintaining a healthy metabolism. In obesity, the increase in fat is associated with impairment in the function of fat, leading to insulin resistance and type 2 diabetes. While some anti-diabetic drugs that improve type 2 diabetes, for example rosiglitazone, work by acting on fat to restore insulin sensitivity, taking these drugs orally can have negative side effects on other parts of the body. In this study, we are using the well-known anti-diabetic drug rosiglitazone to test nanomedicine technology, specifically magnetic nanoparticles, to selectively deliver this drug to fat. This study will allow us to determine if delivering anti-diabetic drugs directly to fat will improve insulin resistance and metabolic function, without inducing negative effects on other tissues in the body. We have previously shown that rosiglitazone can be bound to the nanoparticles, accumulated in fat, and improves insulin resistance in obese mice to a similar degree as mice treated orally with rosiglitazone. This proposal aims to assess how these improvements are occurring and if giving rosiglitazone with the nanoparticles prevents the negative side effects seen in kidney and bone with oral administration. The project will evaluate the potential of nanoparticles for delivering anti-diabetic drugs specifically to fat to improve metabolism. This is a novel therapeutic strategy that could greatly support precision therapeutics for the 11 million Canadians living with type 2 diabetes or pre-diabetes.
Programme
Master's Award: Canada Graduate Scholarships
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
506462
Name
Ostberg Jakob E
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Special Cases - Awards Programs
Projecttitle
Targeted delivery of rosiglitazone to subcutaneous adipose tissue for the treatment of type 2 diabetes
Programtype2
Studentship Programs
Orgnameinp2
University of Northern British Columbia
Cihramount2
$17,500
Cihrequipment2
$0
Programname2
Master's Award: Canada Graduate Scholarships
Keyworddelim
Adipose Tissue Function; Endocrinology; Insulin Resistance; Iron Oxide (Magnetic) Nanoparticles; Nanomedicine; Obesity; Ppargamma; Rosiglitazone; Targeted Therapeutics; Type 2 Diabetes
Abstract
Obesity affects millions of Canadians, increasing the risk for many chronic diseases including type 2 diabetes. Fat, or adipose tissue, plays an important role in maintaining a healthy metabolism. In obesity, the increase in fat is associated with impairment in the function of fat, leading to insulin resistance and type 2 diabetes. While some anti-diabetic drugs that improve type 2 diabetes, for example rosiglitazone, work by acting on fat to restore insulin sensitivity, taking these drugs orally can have negative side effects on other parts of the body. In this study, we are using the well-known anti-diabetic drug rosiglitazone to test nanomedicine technology, specifically magnetic nanoparticles, to selectively deliver this drug to fat. This study will allow us to determine if delivering anti-diabetic drugs directly to fat will improve insulin resistance and metabolic function, without inducing negative effects on other tissues in the body. We have previously shown that rosiglitazone can be bound to the nanoparticles, accumulated in fat, and improves insulin resistance in obese mice to a similar degree as mice treated orally with rosiglitazone. This proposal aims to assess how these improvements are occurring and if giving rosiglitazone with the nanoparticles prevents the negative side effects seen in kidney and bone with oral administration. The project will evaluate the potential of nanoparticles for delivering anti-diabetic drugs specifically to fat to improve metabolism. This is a novel therapeutic strategy that could greatly support precision therapeutics for the 11 million Canadians living with type 2 diabetes or pre-diabetes.
Competitiondate
202312
Approvedterm2
1 yr 0 mth
Pinamesdelim
Ostberg, Jakob E
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $17,500~ $0~