References
- Attias, I. Z.-L., Z. Groswasser, Z. Groswasser, Z. Groswasser, and Z. Groswasser. 2005. Dysfunction of the auditory efferent system in patients with traumatic brain injuries with tinnitus and hyperacusis. J. Basic Clin. Physiol. Pharmacol. 16 (2–3):117–26. doi:https://doi.org/10.1515/JBCPP.2005.16.2-3.117.
- Backoff, P. M., and D. M. Caspary. 1994. Age-related changes in auditory brainstem responses in Fischer 344 rats: Effects of rate and intensity. Hear.Res. 73 (2):163–72. doi:https://doi.org/10.1016/0378-5955(94)90231-3.
- Baldwin, C. M., A. J. Figueredo, L. S. Wright, S. S. Wong, and M. L. Witten. 2007. Repeated aerosol-vapor JP-8 jet fuel exposure affects neurobehavior and neurotransmitter levels in a rat model. J.Toxicology.Env.Health. 70 (14):1203–13. doi:https://doi.org/10.1080/15287390701380872.
- Brandt, A., D. Khimich, and T. Moser. 2005. Few CaV1.3 channels regulate the exocytosis of a synaptic vesicle at the hair cell ribbon synapse. J.Neuro.sci. 25 (50):11577–85. doi:https://doi.org/10.1523/JNEUROSCI.3411-05.2005.
- Brown, D. J., and R. B. Patuzzi. 2010. Evidence that the compound action potential (CAP) from the auditory nerve is a stationary potential generated across dura mater. Hear. Res. 267 (1–2):12–26. doi:https://doi.org/10.1016/j.heares.2010.03.091.
- Burkard, R. F., J. J. Finneran, and J. Mulsow. 2017. The effects of click rate on the auditory brainstem response of bottlenose dolphins. J.Acoustical.Society.Am 141 (5):3396–406. doi:https://doi.org/10.1121/1.4983447.
- Davis, H., B. H. Deatherage, D. H. Eldredge, and C. A. Smith. 1958. Summating potentials of the cochlea. Am.J.Physiol 195 (2):251–61.https://doi.org/10.1152/ajplegacy.1958.195.2.251.
- De Necker, A., L. Biagio-de Jager, and A. C. Stoltz. 2020. Auditory brainstem response test at different stimulus rates in normal-hearing adults living with HIV. Am J.Audiol 29:873–86. doi:https://doi.org/10.1044/2020_AJA-19-00125.
- Delgado, R. E., and O. Ozdamar. 2004. Deconvolution of evoked responses obtained at high stimulus rates. J.Acoustical.Society.Am 115 (3):1242–51. doi:https://doi.org/10.1121/1.1639327.
- Dreisbach, L., S. Murphy, R. Arevalo, C. Schlocker, T. Miller, and O. W. Guthrie. 2022. Is jet fuel exposure associated with central auditory nervous system difficulties: An exploratory study in military personnel. J.Acoustical. Society.Am 151 (3):2027–38. doi:https://doi.org/10.1121/10.0009845.
- Fechter, L. D., J. W. Fisher, G. D. Chapman, V. P. Mokashi, P. A. Ortiz, J. E. Reboulet, J. E. Stubbs, A. M. Lear, S. M. McInturf, S. L. Prues, et al. 2012. Subchronic Jp-8 jet fuel exposure enhances vulnerability to noise-induced hearing loss in rats. J.Toxicology. Env.Health 75 (5):299–317. doi:https://doi.org/10.1080/15287394.2012.652060.
- Fechter, L. D., C. Gearhart, S. Fulton, J. Campbell, J. Fisher, K. Na, D. Cocker, A. Nelson-Miller, P. Moon, and B. Pouyatos. 2007. JP-8 jet fuel can promote auditory impairment resulting from subsequent noise exposure in rats. Toxicological.Sci 98 (2):510–25. doi:https://doi.org/10.1093/toxsci/kfm101.
- Frank, T., D. Khimich, A. Neef, and T. Moser. 2009. Mechanisms contributing to synaptic Ca2+signals and their heterogeneity in hair cells. Proceedings of the National Academy of Sciences U S A 106:4483–88. doi:https://doi.org/10.1073/pnas.0813213106.
- Glowatzki, E., and P. A. Fuchs. 2002. Transmitter release at the hair cell ribbon synapse Nature Neuroscience. Nature Neurosci 5 (2):147–54. doi:https://doi.org/10.1038/nn796.
- Goldstein, M. H., and N. Y. S. Kiang. 1958. Synchrony of neural activity in electric responses evoked by transient acoustic stimuli. J.Acoustical. Society.Am 30 (2):107–14. doi:https://doi.org/10.1121/1.1909497.
- Goutman, J. D., and E. Glowatzki. 2007. Time course and calcium dependence of transmitter release at a single ribbon synapse. Proceedings of the National Academy of Sciences U SA 104:16341–46. doi:https://doi.org/10.1073/pnas.0705756104.
- Groff, J. A., and M. C. Liberman. 2003. Modulation of cochlear afferent response by the lateral olivocochlear system: Activation via electrical stimulation of the inferior colliculus.Journal of Neurophysiology. Journal of Neurophysiology 90 (5):3178–200. doi:https://doi.org/10.1152/jn.00537.2003.
- Guinan, J. J., Jr. 2006. Olivocochlear efferents: Anatomy, physiology, function, and the measurement of efferent effects in humans. Ear Hear 27 (6):589–607. doi:https://doi.org/10.1097/01.aud.0000240507.83072.e7.
- Guthrie, O. W. 2016. Preservation of neural sensitivity after noise-induced suppression of sensory function. J.Am. Acad.Audiol 27 (1):49–61. doi:https://doi.org/10.3766/jaaa.15047.
- Guthrie, O. W. 2017. Functional consequences of inducible genetic elements from the p53 SOS response in a mammalian organ system. Exp.Cell Res. 359 (1):50–61. doi:https://doi.org/10.1016/j.yexcr.2017.08.010.
- Guthrie, O. W., and I. S. Bhatt. 2021. Nondeterministic nature of sensorineural outcomes following noise trauma. Biol Open 10 (10):bio058696. doi:https://doi.org/10.1242/bio.058696.
- Guthrie, O. W., C. Gearhart, S. Fulton, and L. D. Fechter. 2011. Carboxy alkyl esters of Uncaria tomentosa augment recovery of sensorineural functions following noise injury. Brain Res 1407:97–106. doi:https://doi.org/10.1016/j.brainres.2011.06.044.
- Guthrie, O. W., H.-S. Li-Korotky, J. D. Durrant, and C. Balaban. 2008. Cisplatin induces cytoplasmic to nuclear translocation of nucleotide excision repair factors among spiral ganglion neurons. Hear.Res 239 (1–2):79–91. doi:https://doi.org/10.1016/j.heares.2008.01.013.
- Guthrie, O. W., B. A. Wong, S. M. McInturf, and D. R. Mattie. 2022 . Degenerate brainstem circuitry after combined physiochemical exposure to jet fuel and noise. J.Toxicology.Env.Health 85 (5):175–83. doi:https://doi.org/10.1080/15287394.2021.1980166.
- Guthrie, O. W., B. A. Wong, S. M. McInturf, J. E. Reboulet, P. A. Ortiz, and D. R. Mattie. 2015. Inhalation of hydrocarbon jet fuel suppress central auditory nervous system function. J.Toxicology. Envi.Health. 78 (18):1154–69. doi:https://doi.org/10.1080/15287394.2015.1070389.
- Guthrie, O. W., B. A. Wong, S. M. McInturf, J. E. Reboulet, P. A. Ortiz, and D. R. Mattie. 2016. Background noise contributes to organic solvent induced brain dysfunction. Neural.Plast. 2016:8742725. doi:https://doi.org/10.1155/2016/8742725.
- Guthrie, O. W., H. Xu, B. A. Wong, S. M. McInturf, J. E. Reboulet, P. A. Ortiz, and D. R. Mattie. 2014. Exposure to low levels of jet-propulsion fuel impairs brainstem encoding of stimulus intensity. J.Toxicology.Env.Health. 77 (5):261–80. doi:https://doi.org/10.1080/15287394.2013.862892.
- Herrmann, B., S. Yasmin, K. Araz, D. W. Purcell, and I. S. Johnsrude. 2021. Sound level context modulates neural activity in the human brainstem. Sci.Rep 11 (1):22581. doi:https://doi.org/10.1038/s41598-021-02055-y.
- Jafari, Z., B. E. Kolb, and M. H. Mohajerani. 2020. Noise exposure accelerates the risk of cognitive impairment and Alzheimer’s disease: Adulthood, gestational, and prenatal mechanistic evidence from animal studies. Neu.sci.Biobehavioral.Review. 117:110–28. doi:https://doi.org/10.1016/j.neubiorev.2019.04.001.
- Johnson, J. C. S., C. R. Marshall, R. S. Weil, D.-E. Bamiou, C. J. D. Hardy, and J. D. Warren. 2021. Hearing and dementia: From ears to brain. Brain 144 (2):391–401. doi:https://doi.org/10.1093/brain/awaa429.
- Kaf, W. A., K. M. Lewis, E. Yavuz, S. M. Dixon, M. Van Ess, A. M. Jamos, and R. E. Delgado. 2017. Fast click rate electrocochleography and auditory brainstem response in normal-hearing adults using continuous loop averaging deconvolution. Ear.Hear 38 (2):244–54. doi:https://doi.org/10.1097/AUD.0000000000000381.
- Kawase, T., B. Delgutte, and M. C. Liberman. 1993. Antimasking effects of the olivocochlear reflex. II. Enhancement of auditory-nerve response to masked tones. J.Neuro.physiol. 70 (6):2533–49. doi:https://doi.org/10.1152/jn.1993.70.6.2533.
- Keen, E. C., and A. J. Hudspeth. 2006. Transfer characteristics of the hair cell’s afferent synapse. Proceedings of the National Academy of Sciences U S A 103:5537–42. doi:https://doi.org/10.1073/pnas.0601103103.
- Kikidis, D., A. Vardonikolaki, Z. Zachou, A. Razou, P. Pantos, and A. Bibas. 2020. ABR findings in musicians with normal audiogram and otoacoustic emissions: Evidence of cochlear synaptopathy? Hearing, Balance and Communication 18 (1):36–45. doi:https://doi.org/10.1080/21695717.2019.1663054.
- Kral, A., P. A. Yusuf, and R. Land. 2017. Higher-order auditory areas in congenital deafness: Top-down interactions and corticocortical decoupling. Hear.Res. 343:50–63. doi:https://doi.org/10.1016/j.heares.2016.08.017.
- Li, G. L., E. Keen, D. Andor-Ardó, A. J. Hudspeth, and H. von Gersdorff. 2009. The unitary event underlying multiquantal EPSCs at a hair cell’s ribbon synapse. J.Neuro.sci. 29 (23):7558–68. doi:https://doi.org/10.1523/JNEUROSCI.0514-09.2009.
- Liberman, M. C. 1978. Auditory-nerve response from cats raised in a low-noise chamber. J.Acoustical.Society.Am 63 (2):442–55. doi:https://doi.org/10.1121/1.381736.
- Liberman, M. C., M. J. Epstein, S. S. Cleveland, H. Wang, and S. F. Maison. 2016. Toward a differential diagnosis of hidden hearing loss in humans. PLOS ONE 11:e0162726. doi:https://doi.org/10.1371/journal.pone.0162726.
- Martinez-Dunst, C., R. L. Michaels, and P. A. Fuchs. 1997. Release sites and calcium channels in hair cells of the chick’s cochlea. The Journal of Neuroscience 17 (23):9133–44. doi:https://doi.org/10.1523/JNEUROSCI.17-23-09133.1997.
- McMahon, C. M., R. B. Patuzzi, W. P. R. Gibson, and H. Sanli. 2008. Frequency-specifi electrocochleography indicates that presynaptic and postsynaptic mechanisms of auditory neuropathy exist. Ear.Hear 29 (3):314–25. doi:https://doi.org/10.1097/AUD.0b013e3181662c2a.
- Meyer, A. C., T. Frank, D. Khimich, G. Hoch, D. Riedel, N. M. Chapochnikov, Y. M. Yarin, B. Harke, S. W. Hell, A. Egner, et al. 2009. Tuning of synapse number, structure and function in the cochlea. Nat.Neurosci 12 (4):444–53. doi:https://doi.org/10.1038/nn.2293.
- Mørkve, S. H., M. L. Veruki, and E. Hartveit. 2002. Functional characteristics of non-NMD typeionotropic glutamate receptor channels in AII amacrine cells in rat retina. J.Phy. 542 (1):147–65. doi:https://doi.org/10.1113/jphysiol.2002.020305.
- Moser, T., A. Neef, and D. Khimich. 2006. Mechanisms underlying the temporal precision of sound coding at the inner hair cell ribbon synapse. The Journal of Physiology 576 (1):55–62. doi:https://doi.org/10.1113/jphysiol.2006.114835.
- Moser, T., and A. Starr. 2016. Auditory neuropathy-neural and synaptic mechanisms.nature reviews neurology. Nature Reviews. Neurology 12 (3):135–49. doi:https://doi.org/10.1038/nrneurol.2016.10.
- Murugasu, E., and I. J. Russell. 1996. The effect of efferent stimulation on basilar membrane displacement in the basal turn of the Guinea pig cochlea. J.Neuro.sci. 16 (1):325–32. doi:https://doi.org/10.1523/JNEUROSCI.16-01-00325.1996.
- Neef, A., D. Khimich, P. Pirih, D. Riedel, F. Wolf, and T. Moser. 2007. Probing the mechanism of exocytosis at the hair cell ribbon synapse. J.Neuro.sci. 27 (47):12933–44. doi:https://doi.org/10.1523/JNEUROSCI.1996-07.2007.
- Norrix, L. W., and D. Velenovsky. 2018. Clinicians’ guide to obtaining a valid auditory brainstem response to determine hearing status: Signal, noise, and cross-checks. Am.J.Audiol 27 (1):25–36. doi:https://doi.org/10.1044/2017_AJA-17-0074.
- Owusu, E., B. T. Amartey, E. Afutu, and N. Boafo. 2022. Aminoglycoside therapy for tuberculosis: Evidence for ototoxicity among tuberculosis patients in Ghana. Diseases 10 (1):10. doi:https://doi.org/10.3390/diseases10010010.
- Polyakov, A., and H. Pratt. 2003. The cumulative effect of high click rate on monaural and binaural processing in the human auditory brainstem. Clini.Neuro.phy 11 (2):366–75. doi:https://doi.org/10.1016/S1388-2457(02)00372-3.
- Pujol, R., and J. L. Puel. 1999. Excitotoxicity, synaptic repair, and functional recovery in the mammalian cochlea: A review of recent findings. Ann.New York.Acad.Sci 884 (1):249–54. doi:https://doi.org/10.1111/j.1749-6632.1999.tb08646.x.
- Rattay, F., and S. M. Danner. 2014. Peak I of the human auditory brainstem response results from the somatic regions of type I spiral ganglion cells: Evidence from computer modeling. Hear.Res. 315:67–79. doi:https://doi.org/10.1016/j.heares.2014.07.001.
- Ruel, J., R. Nouvian, D. C. Gervais, R. Pujol, M. Eybalin, and J. L. Puel. 2001. Dopamine inhibition of auditory nerve activity in the adult mammalian cochlea. Eur.J.Neuro.sci. 14 (6):977–86. doi:https://doi.org/10.1046/j.0953-816x.2001.01721.x.
- Rüttiger, L., U. Zimmermann, and M. Knipper. 2017. Biomarkers for hearing dysfunction: facts and outlook. J. Oto-Rhino-Laryngology. 79:93–111. doi:https://doi.org/10.1159/000455705.
- Sahley, T. L., D. N. Ph, R. H, and F. E. Musiek. 1997. Efferent auditory system: structure and function. 1st ed. California: Singular Publisher Group.
- Singer, J. H., and J. S. Diamond. 2006. Vesicle depletion and synaptic depression at a mammalian ribbon synapse. J.Neuro.physiol. 95 (5):3191–98. doi:https://doi.org/10.1152/jn.01309.2005.
- Singer, J. H., E. Glowatzki, T. Moser, B. W. Strowbridge, V. Bhandawat, and A. P. Sampath. 2009. Functional properties of synaptic transmission in primary sense organs. J.Neuro.sci. 29 (41):12802–06. doi:https://doi.org/10.1523/JNEUROSCI.3346-09.2009.
- Singer, J. H., L. Lassová, N. Vardi, and J. S. Diamond. 2004. Coordinated multivesicular release at a mammalian ribbon synapse. Nat.Neuro.sci. 7 (8):826–33. doi:https://doi.org/10.1038/nn1280.
- Skoe, E., and J. Tufts. 2018. Evidence of noise-induced subclinical hearing loss using auditory brainstem responses and objective measures of noise exposure in humans. Hear. Res. 361:80–91. doi:https://doi.org/10.1016/j.heares.2018.01.005.
- Stankovic, K. M., and J. J. Guinan . 1999. Medial efferent effects on auditory-nerve responses to tail-frequency tones. I. Rate reduction. J.Acoustical. Society. Am 106 (2):857–69. doi:https://doi.org/10.1121/1.427102.
- Starr, A., T. W. Picton, Y. Sininger, L. J. Hood, and C. I. Berlin. 1996. Auditory neuropathy. Brain 119 (3):741–53. doi:https://doi.org/10.1093/brain/119.3.741.
- Veruki, M. L., S. H. Mørkve, and E. Hartveit. 2003. Functional properties of spontaneous EPSCs and non-NMDA receptors in rod amacrine (AII) cells in the rat retina. J. Physiology. 549 (3):759–74. doi:https://doi.org/10.1113/jphysiol.2003.039982.