Function And Pathophysiological Role Of A Novel Glucose Transporter Expressed In Skeletal Muscle
Funder
National Health and Medical Research Council
Funding Amount
$216,412.00
Summary
Diabetes is a disorder of metabolism resulting from a combination of deficiency of insulin and defective action of the insulin that is present. The most prominent metabolic abnormality is high blood glucose, which is often not satisfactorily corrected by insulin treatment. One of the main reasons for the high blood glucose is reduced uptake of glucose by muscle tissue. The mechanism by which insulin enhances glucose entry into muscle cells involves mobilisation of a specific protein from the glu ....Diabetes is a disorder of metabolism resulting from a combination of deficiency of insulin and defective action of the insulin that is present. The most prominent metabolic abnormality is high blood glucose, which is often not satisfactorily corrected by insulin treatment. One of the main reasons for the high blood glucose is reduced uptake of glucose by muscle tissue. The mechanism by which insulin enhances glucose entry into muscle cells involves mobilisation of a specific protein from the glucose transporter protein family, which has been designated GLUT4. Surprisingly, animals that have been genetically altered to eliminate orknockout GLUT4 production do not develop diabetes. This finding has led to the theory that there is a backup glucose transporter protein that can prevent diabetes when there is a problem with GLUT4 function. We have recently discovered a new member of the glucose transporter protein family that could potentially function as either a parallel or a backup system for GLUT4. This new glucose transporter, which we have called GLUT8, is present in human muscle tissue and studies in other cells have shown that it alters its distribution within the cell in reponse to insulin. We now want to study in more detail the role of this new glucose transporter in muscle tissue and how it functions compared with GLUT4. In particular, we think it is possible that Type 2 diabetes occurs when there is not only a problem with the mobilisation of GLUT4 but also a defect in the production or function of GLUT8. If this is the case, then increasing GLUT8 production might improve glucose transport into muscle tissue and so improve control of blood glucose levels in diabetes.Read moreRead less
Improving The Safety Characteristics Of Lentiviral Vectors.
Funder
National Health and Medical Research Council
Funding Amount
$296,250.00
Summary
Gene therapy holds great promise for the treatment of many types of disease including inherited disorders, cancer and cardiovascular disorders. However, the potential of gene therapy has in many cases been limited by the lack of suitable technologies for gene delivery. We have developed a novel gene delivery vehicle from human immunodeficiency virus type 1 (HIV-1). Although this vehicle has many of the characteristics desired of a gene therapy vector its derivation from a retrovirus, particularl ....Gene therapy holds great promise for the treatment of many types of disease including inherited disorders, cancer and cardiovascular disorders. However, the potential of gene therapy has in many cases been limited by the lack of suitable technologies for gene delivery. We have developed a novel gene delivery vehicle from human immunodeficiency virus type 1 (HIV-1). Although this vehicle has many of the characteristics desired of a gene therapy vector its derivation from a retrovirus, particularly one with such an unenviable reputation, raises obvious safety concerns. In order to properly address this issue it is necessary that the vector is carefully designed and properly tested. This project aims to continue our rational, systematic and stepwise approach to the development of our vector with the aim of producing a vector that can be used with a high degree of confidence in its safety, such that it is suitable for clinical usage. Given the highly desirable properties of these vectors, and the wide range of diseases where their use is being considered, the availability of such a vector will have great significance for the widespread practical application of gene therapy. Indeed, several of the projects we are developing with our vector will in all likelihood lead to lead to clinical trials and it is clear that the conduct of these trials will depend on the availability of a suitable vector.Read moreRead less
Characterisation Of PAR2 Knockout And Transgenic Mice: Towards Gene Therapy For Epithelia Based Inflammatory Diseases
Funder
National Health and Medical Research Council
Funding Amount
$486,943.00
Summary
Debilitating and sometimes fatal diseases like asthma and rheumatoid arthritis urgently require new approaches for their effective management and hopefully, cure. We have recently discovered that the airways posses a powerful and naturally-occuring protective mechanism which is regulated by unique molecules in the membranes of the lining cells of the air passages. These molecules are called protease-activated receptors, or PARs, and are also found on cells lining the inner surfaces of blood vess ....Debilitating and sometimes fatal diseases like asthma and rheumatoid arthritis urgently require new approaches for their effective management and hopefully, cure. We have recently discovered that the airways posses a powerful and naturally-occuring protective mechanism which is regulated by unique molecules in the membranes of the lining cells of the air passages. These molecules are called protease-activated receptors, or PARs, and are also found on cells lining the inner surfaces of blood vessels and joints as well as in skin. We are fortunate to have strains of mice - a species in which the PAR-mediated protective mechanism is well developed - in which the gene for the most important of the PARs found in the lung, PAR2, is missing. These animals are called PAR2 'knock-outs'. We also have another strain of mouse in which the human PAR2 gene has been inserted back into PAR2 knock-out mice. These animals will allow us to determine the importance of PAR2 in protection against asthma, arthritis, vascular disease and deficiencies in skin healing, as well as how PAR2 might be a more effective protective agent in mice rather than humans. Thus, modification of the human gene to make the protective system work as effectively as in the mouse might provide an effective therapy or cure for diseases of the lungs, joints and skin as well as in vascular diseases.Read moreRead less
Management Of Overweight Pre-pubertal Children - A Randomised Controlled Trial
Funder
National Health and Medical Research Council
Funding Amount
$407,300.00
Summary
Obesity is an increasingly common problem in the Australian community, affecting both adults and children. Up to 1 in 4 Australian children are overweight or obese, making it one of the most common chronic disorders in this age-group. Obesity in childhood is associated with such complications as high blood pressure, risk of diabetes, high cholesterol levels, hip, knee and ankle problems, and psychological distress. Given the impact of overweight and obesity on the health of children, how can it ....Obesity is an increasingly common problem in the Australian community, affecting both adults and children. Up to 1 in 4 Australian children are overweight or obese, making it one of the most common chronic disorders in this age-group. Obesity in childhood is associated with such complications as high blood pressure, risk of diabetes, high cholesterol levels, hip, knee and ankle problems, and psychological distress. Given the impact of overweight and obesity on the health of children, how can it be best treated? Surprisingly, there is little information available to guide the management of this common problem. In this study we will test the hypothesis that the addition of a parent skills training program will significantly increase the effectiveness of a diet-activity program designed to reduce weight in overweight 6 to 9-year-olds. Children enrolled in the study will receive one of two interventions (i) parenting + activity-diet or (ii) diet-activity. Parents in the parenting intervention will participate in a parenting skills training program (Triple P) preceding the diet-activity program. Triple P comprises four 2-hour weekly group sessions and four, 15 minute follow-up phone calls which will focus on the skills and strategies required to supervise lifestyle changes. The diet-activity program comprises 8 group sessions for parents over a 5 month period on specific dietary and activity changes and simultaneous structured activity sessions for the children. Success will be judged in several ways. Over a 2 year period, we will monitor the child's weight, self-esteem, sense of well-being, blood pressure and cholesterol levels. We will also monitor the family's functioning and the parents' parenting skills and sense of efficacy. Results from the study should allow us to determine which treatment approach for management of childhood obesity is the most appropriate to be established in community settings.Read moreRead less