Trace Element Regulation In Neurological Disease: From Molecular Pathogenesis To Translational Impact.
Funder
National Health and Medical Research Council
Funding Amount
$631,370.00
Summary
Neurodegenerative diseases such as dementia and motor neuron disease are a major health burden for Australia and new approaches to treatment are urgently required. Essential trace elements such as copper, zinc and iron show major changes in neurodegneration, however, we do not understand how this drives disease processes. This proposal will develop an innovative 3D ‘brain on a chip’ cell model to probe the role of trace elements in brain pathology and identify exciting new treatments options.
Understanding The Roles Of Dendritic Domains In Neuronal Function
Funder
National Health and Medical Research Council
Funding Amount
$491,509.00
Summary
We aim to find cellular basis to cognitive function and dysfunction by understanding the input/output characterstics of individual neurons. Since neurons are fundamental computational units in the brain, we aim to understand how synaptic inputs to different dendritic regions are processed prompting the neuron to fire an output. We also aim to seek distinct roles of certain dendritic branches in gating sensory inputs onto the neuron.
The Function And Modulation Of Dendritic Activity Underlying Neural Circuits And Behavior
Funder
National Health and Medical Research Council
Funding Amount
$450,641.00
Summary
Understanding how brain cells translate sensory input into behaviour is central to explaining how the brain works. My research focuses on the long-standing question of how information from different brain regions is received and processed within individual brain cells. This research is crucial to understanding brain function and can provide a greater understanding of the neuronal processes underlying diseases such as epilepsy, schizophrenia, depression and alcoholism.
A Novel Mechanism For The Maintenance Of Catecholamine Synthesis
Funder
National Health and Medical Research Council
Funding Amount
$356,250.00
Summary
Stress causes an acute response that prepares us for flight or a fight and an adaptive response that requires days to establish. The catecholamines, including adrenaline, noradrenaline and dopamine are critical to both the acute and adaptive stress responses. They are secreted from cells at the level of the nervous system and the adrenal gland. We all respond differently to stress and if we do not cope we can become hypertensive or depressed. These pathologies require drug management and the dru ....Stress causes an acute response that prepares us for flight or a fight and an adaptive response that requires days to establish. The catecholamines, including adrenaline, noradrenaline and dopamine are critical to both the acute and adaptive stress responses. They are secreted from cells at the level of the nervous system and the adrenal gland. We all respond differently to stress and if we do not cope we can become hypertensive or depressed. These pathologies require drug management and the drugs all affect the catecholamine systems. Tyrosine hydroxylase controls catecholamine synthesis and it is activated in both the acute and adaptive phases of the stress response in order to replace catecholamines that have been secreted. Tyrosine hydroxylase is activated by protein phosphorylation in the acute phase and by the synthesis of new tyrosine hydroxylase in the adaptive phase. We have now discovered an additional and novel phase that we refer to as sustained tyrosine hydroxylase activation. This phase spans at least the period between the acute (mins) and adaptive phases (days). It involves the sustained phosphorylation of tyrosine hydroxylase and its mechanism appears to differ from the other two phases. In this project we will answer three questions. Does sustained tyrosine hydroxylase activation: 1 Occur in response to many stimuli and in many catecholamine cell types? 2 Occur by a single mechanism, different to the other phases, in all circumstances? 3 Play a role in the control of blood pressure and depression? This project will provide fundamental data about the mechanisms and consequences of sustained tyrosine hydroxylase activation, which is a part of the stress response not previously discovered. The data may impact on the way we design drugs to control stress responses, including antidepressants and antihypertensives.Read moreRead less