Complement Activation As A Therapeutic Target And Clinical Biomarker For Parkinson's Disease
Funder
National Health and Medical Research Council
Funding Amount
$497,941.00
Summary
Parkinson’s disease is the second most common neurological disease in Australia, yet there is no treatment to slow disease progression. Our study is investigating inflammation within the brain as a major contributing factor in Parkinson’s disease. We will examine this inflammatory pathway in human patients suffering from Parkinson’s, and will test a novel anti-inflammatory drug in animal models of Parkinson’s disease, in order to identify a novel treatment to reduce disease pathology.
Preclinical Development Of Complement C5aR Antagonists For The Treatment Of Motor Neuron Disease
Funder
National Health and Medical Research Council
Funding Amount
$593,326.00
Summary
There is no cure for Motor Neuron Disease (MND) resulting in 2 Australian’s dying each day. Modification of the inflammation is one potential means of slowing MND. Our research team has identified a new series of potent anti-inflammatory compounds that may have potential to treat this disease. Our project will test these compounds in animal models of MND, and validate their usefulness in human MND samples. Ultimately, this work may contribute to the discovery of a new treatment for MND.
Therapeutic Targeting Of Neuroinflammation To Slow The Progression Of Neurodegenerative Disease
Funder
National Health and Medical Research Council
Funding Amount
$463,652.00
Summary
My research has identified key components of our immune system, that can worsen disease in conditions such as Parkinson’s disease and motor neuron disease. I hope that exploring these components in animal models, and patients suffering from these diseases, my group can identify new therapeutic drug candidates that can be progressed in clinical trials. Ultimately, this may lead to new treatments to reduce disease burden in patients suffering from these neurodegenerative conditions.
Defining Reciprocal Neural Circuits That Regulate Appetite And Memory
Funder
National Health and Medical Research Council
Funding Amount
$341,935.00
Summary
How we remember meals influences how much we eat at later time points. This kind of memory likely comes from both the traditional brain areas associated with memory formation, and from areas associated with regulating appetite. How these two brain regions work together to help animals remember what they ate, where they found it, and whether they liked it is not known. This project investigates how these memories are formed and how they are used by animals to make decisions about future meals.
The brain regulates body temperature by a series of mechanisms, including the control of how much blood flows to the skin to lose or retain heat. The project aims to locate the brain temperature receptors and brain pathways that do this, using an animal model, the rat. At present they are not known.
Understanding How The Brain Senses And Encodes Hunger And Satiety
Funder
National Health and Medical Research Council
Funding Amount
$473,477.00
Summary
Obesity is the most important health concern in the world today. Despite all the epidemiology evidence and despite the intervention approaches, obesity and type-2 diabetes continues to rise in Australia and worldwide. Clearly, a greater biological understanding of the mechanisms driving increased calorie intake and decreased calorie expenditure. This fellowship explores the different neural circuits in the brain and how they regulate motivation for food and food consumption
Understanding The Molecular Basis Of Central Nervous System Myelination
Funder
National Health and Medical Research Council
Funding Amount
$408,388.00
Summary
Oligodendrocytes are the cell type in the central nervous system that produce myelin, the insulating layer around nerve cells. Loss of oligodendrocytes and myelin are key features of multiple sclerosis. This project aims to clarify the mechanisms that control the myelination of nerve cells during normal development, allowing the development of strategies to promote myelin repair in human diseases such as Multiple Sclerosis.
Understanding The Contribution Of Iron In Traumatic Brain Injury
Funder
National Health and Medical Research Council
Funding Amount
$601,263.00
Summary
Our group has discovered a novel role of amyloid precursor protein (APP) in cellular iron balance similar to another protein called ceruloplasmin (CP). Both, prevalently found in the brain, convert a damaging iron variety into the safer form. Disruption in either protein leads to cell death. We aim to establish how failure in APP and CP response may be detrimental to traumatic brain injury recovery. Understanding the iron role of APP and CP will lead to therapeutics to counter traumatic injury.
The Role Of Long Noncoding RNAs In Parkinson’s Disease
Funder
National Health and Medical Research Council
Funding Amount
$692,699.00
Summary
Parkinson's disease is a complex neurodegenerative disorder. For 90% of patients there is no known cause and for all patients there is no cure. The development of genome studies and transcriptome sequencing has revealed a class of noncoding RNAs whose regulation or dysregulation may lay at the heart of what goes wrong for PD sufferers. Our laboratory focuses on critical PD genes and their regulation by long noncoding RNAs.
Which Neurons Maintain Sympathetic Vasomotor Tone?
Funder
National Health and Medical Research Council
Funding Amount
$567,918.00
Summary
High blood pressure is a major risk factor for cardiovascular disease, a major burden of disease worldwide. High levels of nerve activity that cause the blood vessels to constrict elevating blood pressure are characteristic of hypertension. We do not know which brain cells set and maintain this nerve activity. We will identify these cells, determine how they function and what regulates them. Ultimately we could control these cells treating the cause of hypertension or when clinical need arises.