I am a neuroscientist working on determining the different pathogenic mechanisms occurring in neurodegenerative movement disorders and dementias, and translating these findings for clinical neurologists and neuropathologists.
Elucidating The Neuroprotective Region Of The Amyloid Precursor Protein (APP) Following Traumatic Brain Injury
Funder
National Health and Medical Research Council
Funding Amount
$467,556.00
Summary
Traumatic brain injury (TBI) is a leading cause of death and disability worldwide and to date there is no therapy to ameliorate this injury. There is increased production of the amyloid precursor protein (APP) following TBI and recent studies have found that APP possesses neuroprotective traits. It is the aim of the current studies to delineate the specific active neuroprotective region of APP and develop them as novel therapeutic interventions for use in TBI.
Finding Clinical Predictors For The Underlying Pathology In Different Frontotemporal Dementia (FTD) Syndromes
Funder
National Health and Medical Research Council
Funding Amount
$136,593.00
Summary
Due to the ageing population in Australia it is predicted that the prevalence of dementia will increase four-fold by 2050. Developing disease-modifying therapies for dementia is therefore a priority, however we also need to be able to accurately identify patients for whom these therapies will be beneficial. Here we will develop strategies for identifying patients with particular protein abnormalities in their brain, the substrate of most therapeutic interventions.
Pericyte Dysfunction Limiting Energy Supply In Alzheimer's Disease
Funder
National Health and Medical Research Council
Funding Amount
$717,708.00
Summary
One possible cause of Alzheimer’s disease (AD) could be narrowing of small blood vessels (capillaries) within the brain, limiting blood flow and energy supply. Pericytes, a cell only on capillaries, maintain blood flow throughout the brain. I believe that pericytes may die in AD leading to an energy deficit and memory problems. I will test using human brains and animal models whether pericyte loss causes AD and how this is happening. Pericytes could provide a new therapy option for AD.
Interleukin-6 -gp130 Signaling And Actions In The CNS
Funder
National Health and Medical Research Council
Funding Amount
$549,092.00
Summary
Interleukin-6 (IL-6) is a member of a family of cytokine proteins that may be causative factors in many neurological disorders where they are involved in diverse processes including inflammation, neuronal injury and repair. In this project we will study how IL-6 affects the brain to bring about these outcomes. The results of this work will advance our understanding of how members of this cytokine family function and how they contribute to neurological disease.
A New Map Of The Human Cerebral Cortex To Assist The Interpretation Of FMRI And PET Studies
Funder
National Health and Medical Research Council
Funding Amount
$264,307.00
Summary
The cortex is the brain structure most intimately involved in cognition, motivation and emotion. It is thought to be the principal area affected in diseases such as schizophrenia, and Alzheimer's disease. An enormous and costly effort is expended in functional neuroimaging with PET and fMRI to establish the relation between cortical regions and neurologic and psychiatric dysfunction. Unfortunately due to the unavailability of an accurate map of the human cortex, the researcher is left only with ....The cortex is the brain structure most intimately involved in cognition, motivation and emotion. It is thought to be the principal area affected in diseases such as schizophrenia, and Alzheimer's disease. An enormous and costly effort is expended in functional neuroimaging with PET and fMRI to establish the relation between cortical regions and neurologic and psychiatric dysfunction. Unfortunately due to the unavailability of an accurate map of the human cortex, the researcher is left only with crude estimates of the location of normal and abnormal cortical activity. Further, there is limited ability to relate the human data to the wealth of knowledge available on non-human primate brains. Conversely, researchers using animal models of human cortical pathology cannot readily relate their data to humans because the similarities between the brains of experimental animals and humans have not yet been comprehensively established. The present project will establish the similarities between the cortex of humans and rhesus monkeys. By revealing comprehensively the location of cortical areas this project will provide the context within which hypotheses of cortical function and dysfunction can be tested. The applicants were the first to use the distribution of chemical substances in the brain to construct a comprehensive map of the rat brain. This work is the only Australian publication ranked amongst the 50 most cited items in the history of science. They wish to apply similar techniques to study the least understood part of the human brain, the cortex. The research proposed herein will not examine human tissue from individuals who suffered from depression, anxiety, schizophrenia, Alzheimer's disease, or Parkinson's disease. However, the outcomes of the proposed research will be of assistance to virtually everyone who studies the relation between these diseases and the brain.Read moreRead less
Brain damage resulting from long-term alcohol abuse is localized to discrete regions of the brain and selectively impairs key neuropsychological functions. Alcohol misuse affects processes that control excitability in the brain, leading to the over-stimulation of brain cells. When this continues for long periods the cells are likely to die and most alcoholics misuse alcohol for most of their adult lives. We will study the human brain s capacity to use and respond to glutamate, its major natural ....Brain damage resulting from long-term alcohol abuse is localized to discrete regions of the brain and selectively impairs key neuropsychological functions. Alcohol misuse affects processes that control excitability in the brain, leading to the over-stimulation of brain cells. When this continues for long periods the cells are likely to die and most alcoholics misuse alcohol for most of their adult lives. We will study the human brain s capacity to use and respond to glutamate, its major natural excitant, in the regions that are selectively damaged by alcoholism. How these capacities are affected by heredity, and by diseases commonly associated with alcoholism such as cirrhosis of the liver, will also be explored. If we can understand how selective brain damage occurs in alcoholics we will be better able to devise new drug therapies to combat and prevent it. As well, localized brain damage is a feature of many neurological diseases, so the study will provide a general model of disease mechanisms.Read moreRead less