scholarly journals Aging of the medial olivocochlear reflex and associations with speech perception

2014 ◽  
Vol 135 (2) ◽  
pp. 754-765 ◽  
Author(s):  
Carolina Abdala ◽  
Sumitrajit Dhar ◽  
Mahnaz Ahmadi ◽  
Ping Luo
2021 ◽  
pp. 108246
Author(s):  
Miriam I. Marrufo-Pérez ◽  
Leire Araquistain-Serrat ◽  
Almudena Eustaquio-Martín ◽  
Enrique A. Lopez-Poveda

2013 ◽  
Vol 34 (5) ◽  
pp. 784-789 ◽  
Author(s):  
Erdem Eren ◽  
Ece Harman ◽  
Seçil Arslanoğlu ◽  
Kazm Önal ◽  
Hüseyin Katlmiş

Author(s):  
Shawn Goodman ◽  
Sriram Boothalingam ◽  
Jeffery T Lichtenhan

Functional outcomes of medial olivocochlear reflex (MOCR) activation, such as improved hearing in background noise and protection from noise damage, involve moderate to high sound levels. Previous noninvasive measurements of MOCR in humans focused primarily on otoacoustic emissions (OAEs) evoked at low sound levels. Interpreting MOCR effects on OAEs at higher levels is complicated by the possibility of the middle-ear muscle reflex and by components of OAEs arising from different locations along the length of the cochlear spiral. We overcame these issues by presenting click stimuli at a very slow rate and by time-frequency windowing the resulting click-evoked (CE)OAEs into short-latency (SL) and long-latency (LL) components. We characterized the effects of MOCR on CEOAE components using multiple measures to more comprehensively assess these effects throughout much of the dynamic range of hearing. These measures included CEOAE amplitude attenuation, equivalent input attenuation, phase, and slope of growth functions. Results show that MOCR effects are smaller on SL components than LL components, consistent with SL components being generated slightly basal of the characteristic frequency region. Amplitude attenuation measures showed the largest effects at the lowest stimulus levels, but slope change and equivalent input attenuation measures did not decrease at higher stimulus levels. These latter measures are less commonly reported and may provide insight into the variability in listening performance and noise susceptibility seen across individuals.


2014 ◽  
Vol 150 (6) ◽  
pp. 1033-1039 ◽  
Author(s):  
Erdem Eren ◽  
Ece Harman ◽  
Seçil Arslanoğlu ◽  
Kazım Önal

2008 ◽  
Vol 13 (5) ◽  
pp. 328-334 ◽  
Author(s):  
Siti Zamratol-Mai Sarah Mukari ◽  
Wan Hasyimah Wan Mamat

2017 ◽  
Vol 348 ◽  
pp. 134-137 ◽  
Author(s):  
Enrique A. Lopez-Poveda ◽  
Almudena Eustaquio-Martín ◽  
Joshua S. Stohl ◽  
Robert D. Wolford ◽  
Reinhold Schatzer ◽  
...  

2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Kristina E. Froud ◽  
Ann Chi Yan Wong ◽  
Jennie M. E. Cederholm ◽  
Matthias Klugmann ◽  
Shaun L. Sandow ◽  
...  

2012 ◽  
Vol 131 (2) ◽  
pp. 1296-1306 ◽  
Author(s):  
Peter G. Jacobs ◽  
Dawn Konrad-Martin ◽  
Garnett P. Mcmillan ◽  
Daniel McDermott ◽  
Stephen A. Fausti ◽  
...  

2021 ◽  
Vol 15 ◽  
Author(s):  
Sriram Boothalingam ◽  
Shawn S. Goodman ◽  
Hilary MacCrae ◽  
Sumitrajit Dhar

The auditory efferent system, especially the medial olivocochlear reflex (MOCR), is implicated in both typical auditory processing and in auditory disorders in animal models. Despite the significant strides in both basic and translational research on the MOCR, its clinical applicability remains under-utilized in humans due to the lack of a recommended clinical method. Conventional tests employ broadband noise in one ear while monitoring change in otoacoustic emissions (OAEs) in the other ear to index efferent activity. These methods, (1) can only assay the contralateral MOCR pathway and (2) are unable to extract the kinetics of the reflexes. We have developed a method that re-purposes the same OAE-evoking click-train to also concurrently elicit bilateral MOCR activity. Data from click-train presentations at 80 dB peSPL at 62.5 Hz in 13 young normal-hearing adults demonstrate the feasibility of our method. Mean MOCR magnitude (1.7 dB) and activation time-constant (0.2 s) are consistent with prior MOCR reports. The data also suggest several advantages of this method including, (1) the ability to monitor MEMR, (2) obtain both magnitude and kinetics (time constants) of the MOCR, (3) visual and statistical confirmation of MOCR activation.


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