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Research Topic : Transmitter biosynthesis
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  • Funded Activity

    Receptor Signalling Through Intracellular Calcium Stores In Chromaffin Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $461,000.00
    Summary
    The function of cells in the body is controlled by many hormones and neurotransmitters acting on the cell's surface. Hormones and transmitters mediate their effects by producing chemical signals within the cell that regulate its activities. One key cell signalling chemical is calcium, especially in nerve cells which have developed sophisticated mechanisms for using calcium to control their function. Recently, new levels of complexity have been discovered, both in how cell calcium levels are modi .... The function of cells in the body is controlled by many hormones and neurotransmitters acting on the cell's surface. Hormones and transmitters mediate their effects by producing chemical signals within the cell that regulate its activities. One key cell signalling chemical is calcium, especially in nerve cells which have developed sophisticated mechanisms for using calcium to control their function. Recently, new levels of complexity have been discovered, both in how cell calcium levels are modified by hormones and transmitters and in how these complex calcium signals are used by cells to control their function. This project will investigate how hormones and transmitters can produce different types of calcium signals in nerve cells, and how these signals affect different aspects of the nerve cell's function. In particular, it will establish how two different types of specialised calcium stores within nerve cells are used by different classes of hormone and transmitter, and the distinct cellular functions these two calcium stores can regulate. The results will provide fundamental new information on how nerve cells control their activity and may help identify potential new targets for drugs.
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    Funded Activity

    Physiology And Pathophysiology Of Autonomic Neurotransmitter Release

    Funder
    National Health and Medical Research Council
    Funding Amount
    $278,392.00
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    Funded Activity

    Physiology And Pathophysiology Of Autonomic Neurotransmitter Release

    Funder
    National Health and Medical Research Council
    Funding Amount
    $271,856.00
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    Funded Activity

    Effect Of Morphine On Substance P Neurones In The Brain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $170,129.00
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    Funded Activity

    Electrical Current Flow In Smooth Muscle During Synapti C Transmission

    Funder
    National Health and Medical Research Council
    Funding Amount
    $108,450.00
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    Funded Activity

    Amplification Of Cardiovascular Noradrenergic Neuroeffector Transmission By Angiotensin II

    Funder
    National Health and Medical Research Council
    Funding Amount
    $262,875.00
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    Funded Activity

    Fatty Acid Biosynthesis In The Malaria Chloroplast As A Drug Target

    Funder
    National Health and Medical Research Council
    Funding Amount
    $131,035.00
    Summary
    Malarial parasites contain a chloroplast similar to that of plants. We recently found genetic evidence suggesting the malaria chloroplast makes fats in the same way as plant chloroplasts. Additionally, we have found that drugs and herbicides that block plant chloroplast fat production stop growth of malaria cultures. Parasitologists had assumed that malaria was unable to make fats and would scavenge them from its human host so we have probably discovered a new metabolic pathway in these parasite .... Malarial parasites contain a chloroplast similar to that of plants. We recently found genetic evidence suggesting the malaria chloroplast makes fats in the same way as plant chloroplasts. Additionally, we have found that drugs and herbicides that block plant chloroplast fat production stop growth of malaria cultures. Parasitologists had assumed that malaria was unable to make fats and would scavenge them from its human host so we have probably discovered a new metabolic pathway in these parasites. We now propose to prove that the drugs work by blocking essential, chloroplast-based fat production in parasites. This could lead to novel treatment of malaria and related parasites.
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    Funded Activity

    Bridging The Gap Between Cartilage Biology And Osteoarthritis Risk Prediction

    Funder
    National Health and Medical Research Council
    Funding Amount
    $512,256.00
    Summary
    Osteoarthritis is a painful and debilitating cartilage disease affecting just under 1 in 10 Australians and costs the Australian economy roughly $12 billion per year. This project will develop computational models of cartilage with the ability to incorporate genetic and environmental risk factors into a predictive model of cartilage disease.
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    Funded Activity

    Analysis Of Bacterial Surface Filaments Important In Infection And Immunity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $161,371.00
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    Funded Activity

    Coenzyme A Synthesis In The Human Malaria Parasite, Plasmodium Falciparum

    Funder
    National Health and Medical Research Council
    Funding Amount
    $428,250.00
    Summary
    Malaria is responsible for hundreds of millions of cases and an estimated 1.5-2.7 million deaths each year. The disease is caused by a microscopic parasite which is becoming increasingly resistant to antimalarial drugs. There is a very real possibility that there will soon be parts of the world in which malaria is an untreatable disease, and there is an urgent need to identify new drug targets. This work focuses on a particular biochemical pathway in the human malaria parasite, Plasmodium falcip .... Malaria is responsible for hundreds of millions of cases and an estimated 1.5-2.7 million deaths each year. The disease is caused by a microscopic parasite which is becoming increasingly resistant to antimalarial drugs. There is a very real possibility that there will soon be parts of the world in which malaria is an untreatable disease, and there is an urgent need to identify new drug targets. This work focuses on a particular biochemical pathway in the human malaria parasite, Plasmodium falciparum. The pathway mediates the conversion of the nutrient, vitamin B5, into a molecule called Coenzyme A. It plays an essential role in the intraerythrocytic parasite and our preliminary data indicate that components of this pathway hold significant potential as antimalarial drug targets. In this project we will use a range of biochemical and molecular biology approaches to characterise in detail the components of this pathway in the parasite and to explore the possibility that compounds that inhibit this pathway may be of value as much-needed new antimalarial agents.
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