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Grant: Operating Grant

University of Alberta

$335,682.00

Molecular characterization of esterase Es-x

EF 2009-10

Résumé
Triacylglycerol (TG, generally referred to as fat) is the most concentrated form of energy storage available for mammals. Excessive fat storage is manifested as obesity, which is a major health problem in Canada. Increased fat storage also augments secretion of lipoproteins carrying bad cholesterol (LDL-cholesterol) into blood stream. High fat levels thus contribute to development of atherosclerosis and heart disease and stroke. Therefore, there is substantial pharmacological interest in enzymes that control TG metabolism in tissues. We have characterized a protein, named Es-x, that plays a role in the intracellular fat metabolism. Our objective is to introduce more of this protein into the liver in animal models and study the effect of this protein on lipid metabolism (fat metabolism in particular). We also plan to investigate lipid metabolism in an animal model in which the protein has been genetically deleted. The research proposed in this application will yield better understanding of how fat metabolism is regulated. The proposed research could become important in designing new therapeutic approaches for decreasing fat synthesis and/or secretion.
Programme
Operating Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
200733
Name
Lehner Richard
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders
Projecttitle
Molecular characterization of esterase Es-x
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$335,682
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Atherosclerosis; Genetic Engineering; Lipolysis; Nafld; Type 2 Diabetes; Vldl Secretion
Abstract
Triacylglycerol (TG, generally referred to as fat) is the most concentrated form of energy storage available for mammals. Excessive fat storage is manifested as obesity, which is a major health problem in Canada. Increased fat storage also augments secretion of lipoproteins carrying bad cholesterol (LDL-cholesterol) into blood stream. High fat levels thus contribute to development of atherosclerosis and heart disease and stroke. Therefore, there is substantial pharmacological interest in enzymes that control TG metabolism in tissues. We have characterized a protein, named Es-x, that plays a role in the intracellular fat metabolism. Our objective is to introduce more of this protein into the liver in animal models and study the effect of this protein on lipid metabolism (fat metabolism in particular). We also plan to investigate lipid metabolism in an animal model in which the protein has been genetically deleted. The research proposed in this application will yield better understanding of how fat metabolism is regulated. The proposed research could become important in designing new therapeutic approaches for decreasing fat synthesis and/or secretion.
Competitiondate
201003
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Lehner, Richard
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $335,682~ $0~