In the areas of the brain where visual information is processed, cells respond to the presentation of visual stimuli by changing their pattern of electrical activity. At the first level of analysis, the primary visual cortex (V1), individual cells become active only if line segments or borders of a particular orientation are present in their field of detection, which encompasses a small part of the visual scene. Cells in other visual cortical areas (the extrastriate cortex) perform more complex ....In the areas of the brain where visual information is processed, cells respond to the presentation of visual stimuli by changing their pattern of electrical activity. At the first level of analysis, the primary visual cortex (V1), individual cells become active only if line segments or borders of a particular orientation are present in their field of detection, which encompasses a small part of the visual scene. Cells in other visual cortical areas (the extrastriate cortex) perform more complex detection tasks in comparison with those in V1, which demand integration of information coming from much larger portions of the visual scene. One example of these more complex properties is the phenomenon of long-range contour integration, where our visual system groups individual line segments having similar orientations, so that they are perceived as part of the same contour. This property is reflected in the electrical responses of cells in the dorsomedial visual area (DM). How are properties such as orientation specificity and long-range contour integration created? To begin addressing this question, we will investigate correlations between the physiological properties of identified cells, the spatial distribution of their information collecting regions (dendrites), and the anatomical pathways by which they receive information from other parts of the brain. This is a basic science study aimed at determining the extent to which the anatomical structure of the brain helps define the function of individual cells and brain areas. Its primary benefit will be to increase our understanding of the mechanisms underlying all sensory processing in the brain. The knowledge obtained may also lead to developments in areas of applied research including medicine and cognitive science (for example, understanding how the brain learns to interpret visual information in early life, and how visual processing degrades with ageing).Read moreRead less
The Role Of Corticothalamic Feedback On The Response Dynamics Of Thalamic Neurons
Funder
National Health and Medical Research Council
Funding Amount
$351,852.00
Summary
A fundamental question in neuroscience is how the brain selectively processes sensory information to generate a reliable representation of the world. Positioned in the centre of the brain, the thalamus plays a key role in sensory processing. This project investigates how the interaction between thalamus and cortex shapes the selection and gating of sensory information. This is a fundamental question in basic neuroscience with the potential to increase our knowledge about attentional deficits.
Does The Complement System Contribute To Neuropathic Pain?
Funder
National Health and Medical Research Council
Funding Amount
$262,958.00
Summary
Nerve injury often results in increased sensitivity to painful stimuli and the perception of innocuous stimuli as painful; it may also result in spontaneous pain. These disorders of pain sensation due to nerve injury are common, debilitating and difficult to treat. They are symptoms of neuropathic pain. Pain is normally signalled to the brain by sensory nerve cells called nociceptors. Following nerve injury, nociceptors are sensitised by chemicals released by inflammatory cells. This contributes ....Nerve injury often results in increased sensitivity to painful stimuli and the perception of innocuous stimuli as painful; it may also result in spontaneous pain. These disorders of pain sensation due to nerve injury are common, debilitating and difficult to treat. They are symptoms of neuropathic pain. Pain is normally signalled to the brain by sensory nerve cells called nociceptors. Following nerve injury, nociceptors are sensitised by chemicals released by inflammatory cells. This contributes to neuropathic pain. We have evidence that inflammatory responses play a key role in initiating neuropathic pain. Other evidence suggests that the immune system contributes to neurological diseases and accompanying pain (e.g. Guillain-Barr syndrome and multiple sclerosis). We plan to test the idea that a component of the immune system known as the complement pathway contributes to the development of neuropathic pain following peripheral nerve injury. The outcome of this work will be a better understanding of the way in which nerve injury leads to chronic disorders of pain, including increased sensitivity to painful stimuli. This will lead in turn to the development of more effective treatments for neuropathic pain.Read moreRead less