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Research Topic : HEPATIC LIPASE
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  • Funded Activity

    The Interaction Of Hepatic Lipase With Heparin And Liver Endothelial Cell Proteoglycans

    Funder
    National Health and Medical Research Council
    Funding Amount
    $134,107.00
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    Funded Activity

    Factors Controlling Lipid Accumulation In Non-adipose Tissues

    Funder
    National Health and Medical Research Council
    Funding Amount
    $463,500.00
    Summary
    The fat cells of the body are designed to store excess fuel for use when supply from the diet is low, or in situations like exercise, demand is high. Fat also accumulates to some extent in the cells of other tissues types, but in some people the accumulation is excessive. This can have a number of serious effects. In the liver and muscle it can interfere with the ability of insulin to properly regulate the amount of glucose present in the blood, contributing to the development of diabetes. In th .... The fat cells of the body are designed to store excess fuel for use when supply from the diet is low, or in situations like exercise, demand is high. Fat also accumulates to some extent in the cells of other tissues types, but in some people the accumulation is excessive. This can have a number of serious effects. In the liver and muscle it can interfere with the ability of insulin to properly regulate the amount of glucose present in the blood, contributing to the development of diabetes. In the liver, fat accumulation can also lead to cirrhosis and liver failure. Cardiovascular complications, resulting in premature death, are also likely. However despite these devastating consequences it is not clear what the underlying cause of the over-accumulation of fat is not known. In this project we will investigate in detail several aspects of fat metabolism that we think are important in controlling how tissues take up fat from the circulation and whether it is subsequently stored or burnt for energy. We will study the amount of fat that is taken up by different tissues of the body under a range of conditions including fed, and short- and long-term fasting. We will also use drugs to inhibit or promote the amount of fat that is burnt, to see if this changes the rate at which fat is taken up by different tissues. In addition we will accelerate, by genetic manipulation, the rate at which some key enzymes of fat metabolism are produced, to determine their effect on the amount of fat that is stored by different tissue types. Our aim is to determine the metabolic processes that influence fat accumulation in those adversely affected tissues such as liver, heart and skeletal muscle. The identification of the most important processes will contribute significantly to the targeting of therapies aimed at preventing excess fat accumulation and its associated diseases.
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    Funded Activity

    Mechanisms Of Lipid Transport In The Blood

    Funder
    National Health and Medical Research Council
    Funding Amount
    $177,945.00
    More information
    Funded Activity

    Why Different Fats Have Different Effects On Blood Cholesterol

    Funder
    National Health and Medical Research Council
    Funding Amount
    $127,180.00
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    Funded Activity

    Are Dietary Fats Cleared Poorly In Subjects With Wasitline Obesity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $213,408.00
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    Funded Activity

    Characterization Of The Activation And Lipid Binding Domains Of Human Apolipoprotein C-II

    Funder
    National Health and Medical Research Council
    Funding Amount
    $194,249.00
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    Funded Activity

    The Alternate Renin Angiotensin System; A Novel Target For The Prevention And Treatment Of Liver Fibrosis And Portal Hypertension

    Funder
    National Health and Medical Research Council
    Funding Amount
    $693,950.00
    Summary
    Cirrhosis of the liver due to chronic hepatitis and other common liver diseases is now a major cause of illness and death in Australia. This project will examine how a hormone system called the renin angiotensin system contributes to the development of liver damage in these diseases. We will study whether drugs targeting this system can be used to reduce liver scarring and prevent the development of cirrhosis and its complications.
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    Funded Activity

    Optimising The Integrity, Function & Durability Of Hepatocytes Used In The Bioartificial Liver

    Funder
    National Health and Medical Research Council
    Funding Amount
    $96,378.00
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    Funded Activity

    Tissue Ferritin Is A Damage-associated Molecular Pattern (DAMP) In Inflammasome-induced Inflammation Associated With Hepatic Stellate Cell Activation And Fibrogenesis In Chronic Liver Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $783,612.00
    Summary
    We have generated considerable evidence for a role for tissue ferritin as a mediator of inflammation associated with liver fibrosis (scarring) These highly novel and innovative studies will assist in identifying pathways involved in the proinflammatory phenotype of hepatic stellate cells (scar-forming cells in the liver) in chronic liver disease and thus will greatly aid in understanding how liver scarring occurs in chronic liver disease.
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    Funded Activity

    Investigation Of The Mechanisms By Which Steatosis Contributes To Hepatic Fibrogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $53,708.00
    More information

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