2020
DOI: 10.1016/j.heares.2020.107883
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Age-related changes in the number of cresyl-violet-stained, parvalbumin and NMDAR 2B expressing neurons in the human spiral ganglion

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Cited by 8 publications
(4 citation statements)
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“…8 H–J ( Xing, et al., 2012 ). These results are consistent with previous human temporal bone studies showing age-related loss of spiral ganglion cells ( Kaur, et al., 2020 ; Makary, et al., 2011 ). In addition, myelin degeneration and myelinated fiber loss identified in the cochleas of the older donors suggests that dysfunction of myelinating Schwann cells may contribute to auditory nerve pathology and the subsequent decline of auditory function in neural presbyacusis.…”
Section: Consequences Of Peripheral Declines and Neural Presbyacusissupporting
confidence: 93%
“…8 H–J ( Xing, et al., 2012 ). These results are consistent with previous human temporal bone studies showing age-related loss of spiral ganglion cells ( Kaur, et al., 2020 ; Makary, et al., 2011 ). In addition, myelin degeneration and myelinated fiber loss identified in the cochleas of the older donors suggests that dysfunction of myelinating Schwann cells may contribute to auditory nerve pathology and the subsequent decline of auditory function in neural presbyacusis.…”
Section: Consequences Of Peripheral Declines and Neural Presbyacusissupporting
confidence: 93%
“…Recent human temporal bone studies demonstrate a sharp decline in spiral ganglion population starting in the mid-fifties with continued decline with increasing age. 48 Human temporal bones with genetic conditions causing loss of hair cells such as Usher 1B (myosin VII mutation) showed significant loss of not only hair cells but also spiral ganglion neurons demonstrating that loss of peripheral trophic support also results in human spiral ganglion loss. 49 This suggests that in humans both aging and loss of trophic support can reduce spiral ganglion populations, which in turn can affect CI outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…It is now widely accepted that over-activation of NMDARs leads to the development of AD ( Xu et al, 2021 ; Abad-Perez et al, 2023 ). However, recent studies have found that NMDARs are not only expressed in the cranial brain, but also in inner hair cells (IHCs), and that overactivation of NMDARs also results in Glu release in IHCs ( Tang et al, 2014 ; Kaur et al, 2020 ; Song et al, 2021 ). Excessive Glu release causes excitatory neurotoxic effects, reducing the number of ribbon synapses in the cochlea and altering synaptic morphology, resulting in impaired signaling of the cochlear nerve and affecting the patient’s hearing ( Hong et al, 2018 ).…”
Section: Hypothesismentioning
confidence: 99%