TY - JOUR
T1 - Noise-induced cochlear synaptopathy
T2 - Past findings and future studies
AU - Kobel, Megan
AU - Le Prell, Colleen G.
AU - Liu, Jennifer
AU - Hawks, John W.
AU - Bao, Jianxin
N1 - Funding Information:
This work was started as a summary update in 2014 for the Newsletter from Department of Defense Hearing Center of Excellence. We would like to thank the members of Animal Model Working Group for their inputs, and particularly Tanisha Hammill and Sara A Murphy for moving this project forward. We would like to thank Drs. Liberman and Ohlemiller for their valuable comments. This work was supported by National Institute on Deafness and other Communication Disorders Grants R01 DC011793 (J.B.) and the Emilie and Phil Schepps Professorship in Hearing Science (C. G. L.)
Publisher Copyright:
© 2016 Elsevier B.V.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - For decades, we have presumed the death of hair cells and spiral ganglion neurons are the main cause of hearing loss and difficulties understanding speech in noise, but new findings suggest synapse loss may be the key contributor. Specifically, recent preclinical studies suggest that the synapses between inner hair cells and spiral ganglion neurons with low spontaneous rates and high thresholds are the most vulnerable subcellular structures, with respect to insults during aging and noise exposure. This cochlear synaptopathy can be “hidden” because this synaptic loss can occur without permanent hearing threshold shifts. This new discovery of synaptic loss opens doors to new research directions. Here, we review a number of recent studies and make suggestions in two critical future research directions. First, based on solid evidence of cochlear synaptopathy in animal models, it is time to apply molecular approaches to identify the underlying molecular mechanisms; improved understanding is necessary for developing rational, effective therapies against this cochlear synaptopathy. Second, in human studies, the data supporting cochlear synaptopathy are indirect although rapid progress has been made. To fully identify changes in function that are directly related this hidden synaptic damage, we argue that a battery of tests including both electrophysiological and behavior tests should be combined for diagnosis of “hidden hearing loss” in clinical studies. This new approach may provide a direct link between cochlear synaptopathy and perceptual difficulties.
AB - For decades, we have presumed the death of hair cells and spiral ganglion neurons are the main cause of hearing loss and difficulties understanding speech in noise, but new findings suggest synapse loss may be the key contributor. Specifically, recent preclinical studies suggest that the synapses between inner hair cells and spiral ganglion neurons with low spontaneous rates and high thresholds are the most vulnerable subcellular structures, with respect to insults during aging and noise exposure. This cochlear synaptopathy can be “hidden” because this synaptic loss can occur without permanent hearing threshold shifts. This new discovery of synaptic loss opens doors to new research directions. Here, we review a number of recent studies and make suggestions in two critical future research directions. First, based on solid evidence of cochlear synaptopathy in animal models, it is time to apply molecular approaches to identify the underlying molecular mechanisms; improved understanding is necessary for developing rational, effective therapies against this cochlear synaptopathy. Second, in human studies, the data supporting cochlear synaptopathy are indirect although rapid progress has been made. To fully identify changes in function that are directly related this hidden synaptic damage, we argue that a battery of tests including both electrophysiological and behavior tests should be combined for diagnosis of “hidden hearing loss” in clinical studies. This new approach may provide a direct link between cochlear synaptopathy and perceptual difficulties.
KW - Hearing loss
KW - Molecular approach
KW - Preclinical model
KW - Spiral ganglion
KW - Synaptic loss
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U2 - 10.1016/j.heares.2016.12.008
DO - 10.1016/j.heares.2016.12.008
M3 - Review article
C2 - 28007526
AN - SCOPUS:85008455595
SN - 0378-5955
VL - 349
SP - 148
EP - 154
JO - Hearing Research
JF - Hearing Research
ER -