Abstract:Otoacoustic emission (OAE) tests of the medial-olivocochlear reflex (MOCR) in humans were assessed for viability as clinical assays. Two reflection-source OAEs [TEOAEs: transient-evoked otoacoustic emissions evoked by a 47 dB sound pressure level (SPL) chirp; and discrete-tone SFOAEs: stimulus-frequency otoacoustic emissions evoked by 40 dB SPL tones, and assessed with a 60 dB SPL suppressor] were compared in 27 normal-hearing adults. The MOCR elicitor was a 60 dB SPL contralateral broadband noise. An estimate… Show more
“…Therefore, the change in CEOAE level due to the presence of IAS and CE-block could arise from transient OAEs and potential SSOAEs caused by IAS and CEblock clicks. SSOAEs were not measured in the current study, however, Marshall et al 35 reported that presence of SSOAEs in their chirp-evoked OAE sample did not affect the observed of MOC inhibition between participants withand without-SSOAEs. Also, considering that the amount of MOC inhibition caused by both IAS and CAS is statistically the same and numerically very similar, it is unlikely that the SSOAEs and transient OAEs evoked by IAS/CE-block clicks, if present, had a large effect on the observed MOC inhibition in the current study.…”
Section: Caveatsmentioning
confidence: 67%
“…However, a recent study tested the influence of SSOAEs on MOC inhibition of CEOAEs, and found no difference in the strength of MOC inhibition between individuals with SSOAEs and individuals with no SSOAEs. 35 This report suggests that the presence of SSOAE in the CEOAE spectrum may not significantly influence the observed MOC inhibition. Most studies that investigate the MOC using clicks have used a 50 Hz click presentation rate as a safe cut-off to avoid evoking ipsilateral MOC activity.…”
Section: A Optimal Click Presentation Ratementioning
Click evoked otoacoustic emissions (CEOAEs) are commonly used both in research and clinics to assay the medial olivocochlear system (MOC). Clicks presented at rates >50 Hz in the contralateral ear have previously been reported to evoke contralateral MOC activity. However, in typical MOC assays, clicks are presented in the ipsilateral ear in conjunction with MOC elicitor (noise) in the contralateral ear. The effect of click rates in such an arrangement is currently unknown. A forward masking paradigm was used to emulate typical MOC assays to elucidate the influence of ipsilateral click presentation rates on MOC inhibition of CEOAEs in 28 normal hearing adults. Influence of five click rates (20.83, 25, 31.25, 41.67, and 62.5 Hz) presented at 55 dB peSPL was tested. Results indicate that click rates as low as 31.25 Hz significantly enhance contralateral MOC inhibition, possibly through the activation of ipsilateral and binaural MOC neurons with potential contributions from the middle ear muscle reflex. Therefore, click rates ≤25 Hz are recommended for use in MOC assays, at least for 55 dB peSPL click level.
“…Therefore, the change in CEOAE level due to the presence of IAS and CE-block could arise from transient OAEs and potential SSOAEs caused by IAS and CEblock clicks. SSOAEs were not measured in the current study, however, Marshall et al 35 reported that presence of SSOAEs in their chirp-evoked OAE sample did not affect the observed of MOC inhibition between participants withand without-SSOAEs. Also, considering that the amount of MOC inhibition caused by both IAS and CAS is statistically the same and numerically very similar, it is unlikely that the SSOAEs and transient OAEs evoked by IAS/CE-block clicks, if present, had a large effect on the observed MOC inhibition in the current study.…”
Section: Caveatsmentioning
confidence: 67%
“…However, a recent study tested the influence of SSOAEs on MOC inhibition of CEOAEs, and found no difference in the strength of MOC inhibition between individuals with SSOAEs and individuals with no SSOAEs. 35 This report suggests that the presence of SSOAE in the CEOAE spectrum may not significantly influence the observed MOC inhibition. Most studies that investigate the MOC using clicks have used a 50 Hz click presentation rate as a safe cut-off to avoid evoking ipsilateral MOC activity.…”
Section: A Optimal Click Presentation Ratementioning
Click evoked otoacoustic emissions (CEOAEs) are commonly used both in research and clinics to assay the medial olivocochlear system (MOC). Clicks presented at rates >50 Hz in the contralateral ear have previously been reported to evoke contralateral MOC activity. However, in typical MOC assays, clicks are presented in the ipsilateral ear in conjunction with MOC elicitor (noise) in the contralateral ear. The effect of click rates in such an arrangement is currently unknown. A forward masking paradigm was used to emulate typical MOC assays to elucidate the influence of ipsilateral click presentation rates on MOC inhibition of CEOAEs in 28 normal hearing adults. Influence of five click rates (20.83, 25, 31.25, 41.67, and 62.5 Hz) presented at 55 dB peSPL was tested. Results indicate that click rates as low as 31.25 Hz significantly enhance contralateral MOC inhibition, possibly through the activation of ipsilateral and binaural MOC neurons with potential contributions from the middle ear muscle reflex. Therefore, click rates ≤25 Hz are recommended for use in MOC assays, at least for 55 dB peSPL click level.
“…Each participant was tested for the presence of spontaneous OAEs (SOAEs) using the synchronized SOAE technique (reported in Marshall et al, 2014). Briefly, responses to 1000 clicks at 55 dB peSPL, presented every 64 ms, were recorded in a linear mode.…”
Section: Recording Of Ceoaesmentioning
confidence: 99%
“…For instance, CEOAE latency can be used to objectively estimate cochlear tuning in the pediatric population, in whom psychophysical tuning curves may be difficult to obtain (Moleti and Sisto, 2003;Moleti et al, 2008). The latency can be applied to accurately characterize the efferent effects on cochlear mechanisms (Francis and Guinan, 2010) and compute a vector metric to index efferent reflex (Abdala et al, 2013;Marshall et al, 2014;Mishra and Abdala, 2015).…”
“…OAE-based measurements have revealed characteristics of MOC reflex tuning (e.g., Veuillet et al 1991; Chéry-Croze et al 1993; Lilaonitkul and Guinan 2007; Zhao & Dhar, 2012), strength (e.g., Backus & Guinan, 2007; Marshall et al, 2014), and the mechanism’s possible involvement in directed auditory attention (e.g., Froehlich et al, 1993; de Boer & Thornton, 2007; Garinis et al, 2011) or listening in noise tasks (e.g., Giraud et al, 1997; Kumar & Vanaja, 2004; de Boer & Thornton, 2008; Smith & Cone, 2015; de Boer et al, 2012). However, a major limitation of this approach is that OAEs are insensitive to MOC reflex effects on the neural ensembles that mediate human hearing, and the functional consequences of this mechanism remain unclear.…”
Distortion product otoacoustic emissions (DPOAEs) and distortion product frequency following responses (DPFFRs) are respectively pre-neural and neural measurements associated with cochlear nonlinearity. Because cochlear nonlinearity is putatively linked to outer hair cell electromotility, DPOAEs and DPFFRs may provide complementary measurements of the human medial olivocochlear (MOC) reflex, which directly modulates outer hair cell function. In this study, we first quantified MOC reflex-induced DPOAE inhibition at spectral fine structure peaks in 22 young human adults with normal hearing. The f1 and f2 tone pairs producing the largest DPOAE fine structure peak for each subject were then used to evoke DPFFRs with and without MOC reflex activation to provide a related neural measure of efferent inhibition. We observed significant positive relationships between DPOAE fine structure peak inhibition and inhibition of DPFFR components representing neural phase locking to f2 and 2f1-f2, but not f1. These findings may support previous observations that the MOC reflex inhibits DPOAE sources differentially. That these effects are maintained and represented in the auditory brainstem suggests that the MOC reflex may exert a potent influence on subsequent subcortical neural representation of sound.
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