David A X Nayagam
B.Sci.(Neuro) / B.Eng.(Elec)(Hons.)
Postgraduate Research Student
Dame Elisabeth Murdoch Scholar
The University of Melbourne - Department of Otolaryngology
2nd Floor, Royal Victorian Eye & Ear Hospital
32 Gisborne Street
East Melbourne VIC 3002
Australia
Ph: +61 3 9929 8462
Fax: +61 3 9663 1958
E-mail: d.nayagam@pgrad.unimelb.edu.au
David Nayagam is a PhD student enrolled through the University of
Melbourne and funded by the Dame Elisabeth Murdoch Scholarship administered
by the Bionic Ear Institute. His supervisors are Dr. Tony Paolini,
Dr. Janine Clarey, Dr. Anthony Burkitt and Prof. Graeme Clark.
The current project, conducted as a basis for David’s PhD thesis
has investigated a brainstem region that is important in a pattern
recognition pathway from the cochlear nucleus to the midbrain. This
region - the ventral nucleus of the lateral lemniscus (VNLL) - receives
input from a small but distinct area of the cochlear nucleus (the first
processing point for signals from the inner ear) that is known to be
sensitive to the onsets of broadband sounds and amplitude modulated
(AM) signals. There has been relatively little research of the VNLL,
so David’s work has first sought to describe this region in terms
of its functional organisation and response properties to simple sounds.
He has generated 3-D maps of the VNLL to examine its frequency organisation,
the distribution of different response types, and whether cells response
to only one or both ears. He has correlated physiology with morphology
by filling cells with a dye after intracellular electrophysiological
identification of a given cell. Experiments have also investigated
the responses of these neurons to AM tones. He has found that many
of the VNLL cells respond to AM signals with responses that are locked
to the modulation frequency. In simple terms, this means that these
cells are in effect ‘demodulating’ AM stimuli in much the
same way as an AM radio would. This feature extraction may be important
in processing human speech, which contains AM components. One of the
novel findings from this project is a subset of VNLL cells that receive
fast inhibitory inputs before showing an excitatory response to pure
tones. As there are no known incoming inhibitory signals that could
account for this finding, a network within the VNLL that rapidly converts
incoming excitation into powerful onset inhibition is the favoured
explanation. As an outcome of this proposed network, the origins of
certain response patterns both in the VNLL and the midbrain may be
resolved. These findings have recently been published in the Journal
of Neurophysiology.
Currently David is writing his thesis and preparing manuscripts, having
completed the experimental phase of his project. He is also planning
a trip to the United States in early 2006 to present his findings at
an international conference as well as to visit several world leaders
in his field.
On a personal note, David loves music - playing lead guitar in an
awesome Melbourne rock band (http://www.diane-young.com). He also enjoys skiing,
table tennis, SCUBA diving, hang-gliding, films, television and sleeping – especially
sleeping.
Publications & Presentations:
Nayagam, D.A., Clarey J.C., Paolini A.G. (2005). "Powerful, Onset
Inhibition in the Ventral Nucleus of the Lateral Lemniscus." J
Neurophysiol 94:1651-1654.
Nayagam, D.A (2005) "Powerful, Fast Inhibition Controls Spike
Timing in the Auditory Brainstem." 2nd Australasian Auditory Neuroscience
Workshop. Invited Speaker.
Nayagam, D.A., Paolini, A.G., Clarey, J.C., Burkitt, A.N., Clark,
G.M. (2005). "Powerful, Fast Inhibition Controls First-Spike Timing
In The Auditory Brainstem." Proceedings of the Australian Neuroscience
Society 16:P175.
Nayagam, D.A., Paolini, A.G., Clarey, J.C., Burkitt, A.N., Clark,
G.M. (2004). “Functional Organisation of the Rat Ventral Nucleus
of the Lateral Lemniscus.” Proceedings of the Australian Neuroscience
Society 15:P167.
Nayagam, D. A., Paolini, A.G., Clarey, J.C., Burkitt, A.N., Clark,
G.M. (2003). “Intracellular and Extracellular Responses of Single
Neurons in the Ventral Nucleus of the Lateral Lemniscus.” Proceedings
of the Australian Neuroscience Society 14:P265.