Mapping sites of visceral convergence connecting the colon and bladder. This project aims to develop multiple neuroanatomical approaches to identify where in the central nervous system the sensory signalling from the colon and bladder merge. The combination of such technologies is novel to the study of the central circuits relaying colon/bladder convergence into the brain and will generate new and detailed knowledge of the central pathways in which pelvic organ sensory (discomfort) and motor (de ....Mapping sites of visceral convergence connecting the colon and bladder. This project aims to develop multiple neuroanatomical approaches to identify where in the central nervous system the sensory signalling from the colon and bladder merge. The combination of such technologies is novel to the study of the central circuits relaying colon/bladder convergence into the brain and will generate new and detailed knowledge of the central pathways in which pelvic organ sensory (discomfort) and motor (defecation/urination) functions are coordinated. The expected outcomes are predicted to aid future discovery of mechanisms of cross-organ sensitisation and are anticipated to provide significant benefit to therapy development for chronic visceral pain syndromes associated with bowel and bladder dysfunction.Read moreRead less
The jugular vagal sensory connectome regulating visceral function. Internal body organs have a rich supply of sensory nerve fibres that serve important roles in monitoring the local environment for normal and abnormal sensory stimuli. These nerve fibres have different origins and wire into brain circuits that regulate widely diverse physiological responses. In this study we aim to study the neural circuits and responses mediated by a group of these sensory nerves which has not been investigated ....The jugular vagal sensory connectome regulating visceral function. Internal body organs have a rich supply of sensory nerve fibres that serve important roles in monitoring the local environment for normal and abnormal sensory stimuli. These nerve fibres have different origins and wire into brain circuits that regulate widely diverse physiological responses. In this study we aim to study the neural circuits and responses mediated by a group of these sensory nerves which has not been investigated appreciably in the past. We believe that these sensory neural circuits will reveal important new insights into how internal organs perform their diverse and essential functions to sustain life.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE230101079
Funder
Australian Research Council
Funding Amount
$453,528.00
Summary
New insights into how the brain interprets visceral and somatic sensations. Sensory nerve fibres monitor normal and abnormal stimuli in our body tissues, sending this information to the brain. I study the sensory pathways of the respiratory system which protect the lungs from harmful stimuli, such as inhaled pollutants or smoke. I discovered that respiratory sensory pathways interact with sensory circuits in the brain arising from other body tissues. The goal of this project is to investigate on ....New insights into how the brain interprets visceral and somatic sensations. Sensory nerve fibres monitor normal and abnormal stimuli in our body tissues, sending this information to the brain. I study the sensory pathways of the respiratory system which protect the lungs from harmful stimuli, such as inhaled pollutants or smoke. I discovered that respiratory sensory pathways interact with sensory circuits in the brain arising from other body tissues. The goal of this project is to investigate one example of this interaction; the convergence of visceral and somatic sensory pathways onto a brain circuit that regulates the intensity of the sensations that are experienced. This project addresses the fundamental question of how the brain processes two competing noxious sensations.Read moreRead less
Understanding multiday cycles underpinning human physiology. We recently discovered long-term rhythms modulating activities of our brains and hearts ranging in duration from 3-60 days. The cause of these longer, ‘multiday cycles’ remain unknown. This project aims to understand; causes of multiday cycles (measuring the nervous and autonomic nervous system), their effects (on cognition, sleep, and stress), and quantify the relationship between coupled cyclical systems. The research outcomes can pr ....Understanding multiday cycles underpinning human physiology. We recently discovered long-term rhythms modulating activities of our brains and hearts ranging in duration from 3-60 days. The cause of these longer, ‘multiday cycles’ remain unknown. This project aims to understand; causes of multiday cycles (measuring the nervous and autonomic nervous system), their effects (on cognition, sleep, and stress), and quantify the relationship between coupled cyclical systems. The research outcomes can provide fundamental new knowledge about cyclic dynamics governing human physiology, leading to improved rigour in life sciences research. Commercial outcomes include technology to optimise individual productivity, learning, health, and wellbeing based on physiological cycles, with diverse benefits to society.Read moreRead less
Unravelling the brain circuits linking emotions and heart rate variability. We are all familiar with the rapid breathing and heart pounding that occurs when we are frightened. Is the feeling of panic because we sense our heart pounding, or does our heart pound because we panic? This age-old question has resisted attempts to understand its neurobiological basis. This project aims to address this lack of knowledge using novel cutting-edge neuroscience methods that enable mapping of connected brain ....Unravelling the brain circuits linking emotions and heart rate variability. We are all familiar with the rapid breathing and heart pounding that occurs when we are frightened. Is the feeling of panic because we sense our heart pounding, or does our heart pound because we panic? This age-old question has resisted attempts to understand its neurobiological basis. This project aims to address this lack of knowledge using novel cutting-edge neuroscience methods that enable mapping of connected brain pathways and the ability to change the activity of specific brain cells with millisecond time resolution. The project will identify, and functionally characterise, the link between the heart and emotions, to gain new insights into the interaction between the autonomic nervous system and disordered emotional regulation.Read moreRead less
Platform technology to decode motor control through ultra high-field MRI. This project aims to advance our understanding of the poorly understood neural circuits that enable fine motor control in humans. To obtain this knowledge, new platform technology will be developed to capture the full kinematics of the hand during concurrent functional magnetic resonance imaging at ultra high-field. This device will allow testing of fundamental theories describing the canonical microcircuits involved in ha ....Platform technology to decode motor control through ultra high-field MRI. This project aims to advance our understanding of the poorly understood neural circuits that enable fine motor control in humans. To obtain this knowledge, new platform technology will be developed to capture the full kinematics of the hand during concurrent functional magnetic resonance imaging at ultra high-field. This device will allow testing of fundamental theories describing the canonical microcircuits involved in hand motion. Expected outcomes include new evidence of mirror neurons and observation of predictive error signals in the motor cortex. This new knowledge paves the way towards improved computer-brain interface technology which is likely to create benefits through translation to applications such as artificial limb control.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE200101272
Funder
Australian Research Council
Funding Amount
$420,885.00
Summary
Glial Plasticity: How experience and aging change brain structure. 50 % of the cells in the brain are called glia. These cells work with neurons to regulate how we think, feel and behave. Most glial cells are added to the brain after birth, however we know very little about how this process works, or how it may be changed by lived-experience. The overarching aim of this study is to better understand how lived-experience impacts the growth of the major types of glial cells in the brain. To do th ....Glial Plasticity: How experience and aging change brain structure. 50 % of the cells in the brain are called glia. These cells work with neurons to regulate how we think, feel and behave. Most glial cells are added to the brain after birth, however we know very little about how this process works, or how it may be changed by lived-experience. The overarching aim of this study is to better understand how lived-experience impacts the growth of the major types of glial cells in the brain. To do this, I will use cutting-edge technologies and identify; 1) the rates of cell growth for the major types of glia, and 2) map how they are integrated into the brain. This will lead to important new information on how lived-experience can shape the growth and structure of the brain.Read moreRead less
Phenotyping doublecortin+ cells to unravel human adult neurogenesis. This project investigates one of the brain’s most remarkable phenomena: adult neurogenesis, the birth of new brain cells in a specialised brain area (the hippocampus) occurring well into adulthood. This process contributes to many species’ capacity to learn, remember and regenerate. However whether this process occurs in humans is heavily debated. Using new neuroscience tools, this project will produce new insights into human a ....Phenotyping doublecortin+ cells to unravel human adult neurogenesis. This project investigates one of the brain’s most remarkable phenomena: adult neurogenesis, the birth of new brain cells in a specialised brain area (the hippocampus) occurring well into adulthood. This process contributes to many species’ capacity to learn, remember and regenerate. However whether this process occurs in humans is heavily debated. Using new neuroscience tools, this project will produce new insights into human adult neurogenesis by deeply examining hippocampal cells that express the newborn cell marker, doublecortin. This will enable clarification of the existence and extent of adult neurogenesis in humans, and provide the foundation to leverage this process for improving learning, memory and brain regeneration in people.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE190100269
Funder
Australian Research Council
Funding Amount
$422,232.00
Summary
Mapping the neural circuits which control water and salt intake. This project aims to map the brain circuits controlling fluid and salt intake using innovative genetically encoded techniques, which enable precise targeting and manipulation of select neuronal populations. Expected outcomes of this project include constructing detailed maps of the brain circuits for fluid and salt intake by tracing multiple nodes in the network, characterising neuronal populations, and precisely defining their fun ....Mapping the neural circuits which control water and salt intake. This project aims to map the brain circuits controlling fluid and salt intake using innovative genetically encoded techniques, which enable precise targeting and manipulation of select neuronal populations. Expected outcomes of this project include constructing detailed maps of the brain circuits for fluid and salt intake by tracing multiple nodes in the network, characterising neuronal populations, and precisely defining their functions. This should provide significant benefits including understanding the brain regions controlling fluid and salt intake which are essential for maintaining fluid homeostasis, and providing a framework for investigating the neural circuits underlying other complex behaviours.Read moreRead less