Brain Circuits for Hearing Group


Our research focuses on dissecting the neural pathways—the “wiring diagram” of the brain—that transmit information about sound.  How are auditory circuits, and their targets, organised with respect to sensory parameters, such as sound frequency or intensity?  How does this organisation facilitate sensory processing?  Most importantly, what happens to these pathways when sensory input becomes disrupted with hearing loss?

The brain is a remarkable machine that allows us to sift through a bewildering array of information—sights, sounds, smells, etc.—we receive about our surrounding environment at any given moment.  Encoded by sequences of neural “spikes”, this information is extensively processed and interpreted by the brain to construct an internal representation of a coherent and stable external reality.  The desire to understand how the brain achieves this feat has inspired decades of neuroscientific research, yet many details remain elusive.  Part of this challenge lies in the immense complexity of the task: the human brain contains ~86 billion neurons, and every single one can be considered unique with respect to chemical composition, genetic signature, and most importantly, connectivity with other neurons.

Our working hypothesis is that abnormalities in the central auditory system underlie some of the major symptoms of hearing loss.  Hearing loss interferes with the quality of information sent from our ears to the brain.  If the loss occurs at an early age, the brain may fail to assemble its auditory circuits correctly.  More commonly, however, hearing loss occurs later in life, after our hearing circuits have already been organised.  What we are beginning to understand is that normal hearing is also required throughout our lifetime for maintaining the brain’s ability to process sounds, such as understanding speech in a noisy environment.  Following a gradual and prolonged reduction of auditory input, the system may begin to change in ways we do not yet fully understand.

Our group investigates these issues using mouse models of hearing and hearing loss.  We use electrophysiology to measure hearing function (e.g., audiometric thresholds, frequency tuning).  We then inject tracer dyes into structures of interest to label neural circuits linked to these measurements, allowing us to investigate structure-function relationships in the brain.  We use a combination of light, fluorescent, and electron microscopy to explore connectivity at both macroscopic (e.g., frequency organisation within a nuclei) and microscopic (e.g., synaptic connectivity between nuclei) levels.  Furthermore, we have developed programs to automate the assembly of large digital image sets and efficiently reconstruct neuroanatomical data in 3D.  By comparing the organisation of inputs, their physiology, and target cell types, we can begin to develop hypotheses as to how these circuits compute and propagate representations of sound events, and how they become compromised with hearing loss.  We are exploring the potential for early intervention (e.g., hearing aids) at mitigating or restoring pathological changes in the brain that result from prolonged hearing loss.  By understanding the nature of such changes in the brain, we may be able to improve the strategy and design of future generations of hearing aids and better inform clinical treatment timelines.

Selected Publications

Schrode KM, Muniak MA, Kim Y-H, Lauer AM (2018) Central compensation in auditory brainstem after damaging noise exposure. eNeuro 10.1523/ENEURO.0250-18.2018

Muniak MA, Ayeni FE, Ryugo DK (2018) Hidden hearing loss and endbulbs of Held: Evidence for central pathology before detection of ABR threshold increases. Hearing Research 364:104-117.

Milinkeviciute G, Muniak MA, Ryugo DK (2017) Descending projections from the inferior colliculus to the dorsal cochlear nucleus are excitatory. Journal of Comparative Neurology 525(4):773.93.

Connelly CJ, Ryugo DK, Muniak MA (2017) The effect of progressive hearing loss on the morphology of endbulbs of Held and bushy cells. Hearing Research 343:14-33.

Muniak MA, Connelly CJ, Suthakar K, Milinkeviciute G, Ayeni FE, Ryugo DK (2016) Central projections of spiral ganglion neurons.  In: Dabdoub A, Fritzsch B, Popper AN, Fay RR, eds.  Springer Handbook of Auditory Research: The Primary Auditory Neurons of the Mammalian Cochlea.  Springer: New York.

Muniak MA, Ryugo DK (2014) Tonotopic organization of vertical cells in the dorsal cochlear nucleus of the CBA/J mouse. Journal of Comparative Neurology 522(4):937-49.

Muniak MA, Connelly CJ, Tirko NN, O'Neil JN, Ryugo DK (2013) Synaptic organization and plasticity in the auditory system of the deaf white cat.  In: Kral A, Popper AN, Fay RR, eds.  Springer Handbook of Auditory Research: Deafness.  Springer: New York.

Muniak MA, Rivas A, Montey KL, May BJ, Francis HW, Ryugo DK (2013) 3D Model of Frequency Representation in the Cochlear Nucleus of the CBA/J Mouse. Journal of Comparative Neurology 521(7):1510-32.

Muniak MA, Mayko ZM, Ryugo DK, Portfors CV (2012) Preparation of an awake mouse for recording neural responses and injecting tracers. Journal of Visualized Experiments (64):e3755.

Nayagam BA, Muniak MA, Ryugo DK (2011) The spiral ganglion: Connecting the peripheral and central auditory systems. Hearing Research 278(1-2):2-20.

More Garvan Publications

Staff in the Group