The medial olivocochlear reflex strength is modulated during a visual working memory task

The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found...

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Published inJournal of neurophysiology Vol. 125; no. 6; pp. 2309 - 2321
Main Authors Marcenaro, Bruno, Leiva, Alexis, Dragicevic, Constantino, López, Vladimir, Delano, Paul H.
Format Journal Article
LanguageEnglish
Published United States 01.06.2021
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Abstract The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory. Top-down modulation of sensory responses to distracting stimuli by selective attention has been proposed as an important mechanism by which our brain can maintain relevant information during working memory tasks. Previous works in visual working memory (VWM) have reported modulation of neural responses to distracting sounds at different levels of the central auditory pathways. Whether these modulations occur also at the level of the auditory receptor is unknown. Here, we hypothesize that cochlear responses to irrelevant auditory stimuli can be modulated by the medial olivocochlear system during VWM. Twenty-one subjects (13 males, mean age 25.3 yr) with normal hearing performed a visual change detection task with different VWM load conditions (high load = 4 visual objects; low load = 2 visual objects). Auditory stimuli were presented as distractors and allowed the measurement of distortion product otoacoustic emissions (DPOAEs) and scalp auditory evoked potentials. In addition, the medial olivocochlear reflex strength was evaluated by adding contralateral acoustic stimulation. We found larger contralateral acoustic suppression of DPOAEs during the visual working memory period ( n = 21) compared with control experiments ( n = 10), in which individuals were passively exposed to the same experimental conditions. These results show that during the visual working memory period there is a modulation of the medial olivocochlear reflex strength, suggesting a possible common mechanism for top-down filtering of auditory responses during cognitive processes. NEW & NOTEWORTHY The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory.
AbstractList Top-down modulation of sensory responses to distracting stimuli by selective attention has been proposed as an important mechanism by which our brain can maintain relevant information during working memory tasks. Previous works in visual working memory (VWM) have reported modulation of neural responses to distracting sounds at different levels of the central auditory pathways. Whether these modulations occur also at the level of the auditory receptor is unknown. Here, we hypothesize that cochlear responses to irrelevant auditory stimuli can be modulated by the medial olivocochlear system during VWM. Twenty-one subjects (13 males, mean age 25.3 yr) with normal hearing performed a visual change detection task with different VWM load conditions (high load = 4 visual objects; low load = 2 visual objects). Auditory stimuli were presented as distractors and allowed the measurement of distortion product otoacoustic emissions (DPOAEs) and scalp auditory evoked potentials. In addition, the medial olivocochlear reflex strength was evaluated by adding contralateral acoustic stimulation. We found larger contralateral acoustic suppression of DPOAEs during the visual working memory period ( = 21) compared with control experiments ( = 10), in which individuals were passively exposed to the same experimental conditions. These results show that during the visual working memory period there is a modulation of the medial olivocochlear reflex strength, suggesting a possible common mechanism for top-down filtering of auditory responses during cognitive processes. The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory.
Top-down modulation of sensory responses to distracting stimuli by selective attention has been proposed as an important mechanism by which our brain can maintain relevant information during working memory tasks. Previous works in visual working memory (VWM) have reported modulation of neural responses to distracting sounds at different levels of the central auditory pathways. Whether these modulations occur also at the level of the auditory receptor is unknown. Here, we hypothesize that cochlear responses to irrelevant auditory stimuli can be modulated by the medial olivocochlear system during VWM. Twenty-one subjects (13 males, mean age 25.3 yr) with normal hearing performed a visual change detection task with different VWM load conditions (high load = 4 visual objects; low load = 2 visual objects). Auditory stimuli were presented as distractors and allowed the measurement of distortion product otoacoustic emissions (DPOAEs) and scalp auditory evoked potentials. In addition, the medial olivocochlear reflex strength was evaluated by adding contralateral acoustic stimulation. We found larger contralateral acoustic suppression of DPOAEs during the visual working memory period (n = 21) compared with control experiments (n = 10), in which individuals were passively exposed to the same experimental conditions. These results show that during the visual working memory period there is a modulation of the medial olivocochlear reflex strength, suggesting a possible common mechanism for top-down filtering of auditory responses during cognitive processes.NEW & NOTEWORTHY The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory.Top-down modulation of sensory responses to distracting stimuli by selective attention has been proposed as an important mechanism by which our brain can maintain relevant information during working memory tasks. Previous works in visual working memory (VWM) have reported modulation of neural responses to distracting sounds at different levels of the central auditory pathways. Whether these modulations occur also at the level of the auditory receptor is unknown. Here, we hypothesize that cochlear responses to irrelevant auditory stimuli can be modulated by the medial olivocochlear system during VWM. Twenty-one subjects (13 males, mean age 25.3 yr) with normal hearing performed a visual change detection task with different VWM load conditions (high load = 4 visual objects; low load = 2 visual objects). Auditory stimuli were presented as distractors and allowed the measurement of distortion product otoacoustic emissions (DPOAEs) and scalp auditory evoked potentials. In addition, the medial olivocochlear reflex strength was evaluated by adding contralateral acoustic stimulation. We found larger contralateral acoustic suppression of DPOAEs during the visual working memory period (n = 21) compared with control experiments (n = 10), in which individuals were passively exposed to the same experimental conditions. These results show that during the visual working memory period there is a modulation of the medial olivocochlear reflex strength, suggesting a possible common mechanism for top-down filtering of auditory responses during cognitive processes.NEW & NOTEWORTHY The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory.
The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory. Top-down modulation of sensory responses to distracting stimuli by selective attention has been proposed as an important mechanism by which our brain can maintain relevant information during working memory tasks. Previous works in visual working memory (VWM) have reported modulation of neural responses to distracting sounds at different levels of the central auditory pathways. Whether these modulations occur also at the level of the auditory receptor is unknown. Here, we hypothesize that cochlear responses to irrelevant auditory stimuli can be modulated by the medial olivocochlear system during VWM. Twenty-one subjects (13 males, mean age 25.3 yr) with normal hearing performed a visual change detection task with different VWM load conditions (high load = 4 visual objects; low load = 2 visual objects). Auditory stimuli were presented as distractors and allowed the measurement of distortion product otoacoustic emissions (DPOAEs) and scalp auditory evoked potentials. In addition, the medial olivocochlear reflex strength was evaluated by adding contralateral acoustic stimulation. We found larger contralateral acoustic suppression of DPOAEs during the visual working memory period ( n = 21) compared with control experiments ( n = 10), in which individuals were passively exposed to the same experimental conditions. These results show that during the visual working memory period there is a modulation of the medial olivocochlear reflex strength, suggesting a possible common mechanism for top-down filtering of auditory responses during cognitive processes. NEW & NOTEWORTHY The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded electroencephalographic activity and otoacoustic emissions in response to auditory distractors during a visual working memory task in humans. We found that the olivocochlear efferent activity is modulated during the visual working memory period suggesting a common mechanism for suppressing cochlear responses during selective attention and working memory.
Author Marcenaro, Bruno
López, Vladimir
Dragicevic, Constantino
Delano, Paul H.
Leiva, Alexis
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Cites_doi 10.1038/36846
10.1016/s0021-9924(98)00019-7
10.3389/fnsys.2015.00134
10.1523/JNEUROSCI.1436-19.2019
10.1038/s41598-020-71399-8
10.1016/s0926-6410(03)00137-x
10.1002/cne.20550
10.1038/nature04171
10.3389/fpsyg.2012.00030
10.1016/j.cophys.2020.08.016
10.1371/journal.pone.0052267
10.1523/JNEUROSCI.4031-15.2016
10.1111/ejn.12746
10.1073/pnas.94.20.10979
10.3389/fnhum.2016.00380
10.3758/s13423-011-0055-3
10.3758/bf03208800
10.1007/s00359-008-0340-4
10.1523/JNEUROSCI.4861-13.2014
10.1371/journal.pone.0155991
10.1046/j.1365-2273.2002.00541.x
10.1037/a0037163
10.1016/j.neubiorev.2019.03.017
10.1016/0014-4886(71)90003-3
10.1017/s0140525x01003922
10.4324/9781315625560
10.1016/j.neuroscience.2012.07.062
10.1152/physrev.2001.81.3.1305
10.1121/1.414508
10.1111/j.1469-8986.2009.00845.x
10.1016/j.heares.2019.04.010
10.1097/AUD.0b013e31827ada02
10.1152/jn.1997.77.5.2385
10.1038/nn.3655
10.1016/j.neuron.2018.09.023
10.1523/JNEUROSCI.20-12-04701.2000
10.1097/00001756-200003200-00043
10.1016/j.tics.2011.11.014
10.3389/fnhum.2016.00221
10.1037/xhp0000413
10.1016/j.jneumeth.2003.10.009
10.1016/j.heares.2017.02.003
10.1162/jocn_a_00275
10.1111/j.1467-7687.2007.00619.x
10.1016/j.jesp.2013.03.013
10.1016/j.neuroimage.2006.07.015
10.1016/0031-9384(95)00012-8
10.1007/s12311-015-0694-4
10.55782/ane-2012-1902
10.1186/s12915-021-00992-8
10.1038/349413a0
10.1371/journal.pone.0165645
10.3389/fnsys.2018.00042
10.1093/cercor/bhj035
10.1523/JNEUROSCI.3702-06.2007
10.1371/journal.pone.0208939
10.1016/j.clinph.2003.11.021
10.1016/j.ijpsycho.2014.09.012
10.1007/s11065-012-9202-5
10.1007/s10162-015-0509-9
10.1073/pnas.1523471113
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working memory
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Schochat E (B44) 2012; 72
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Cowan N (B7) 2016
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B54
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References_xml – ident: B26
  doi: 10.1038/36846
– ident: B45
  doi: 10.1016/s0021-9924(98)00019-7
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  doi: 10.3389/fnsys.2015.00134
– ident: B61
  doi: 10.1523/JNEUROSCI.1436-19.2019
– ident: B58
  doi: 10.1038/s41598-020-71399-8
– ident: B35
  doi: 10.1016/s0926-6410(03)00137-x
– ident: B46
  doi: 10.1002/cne.20550
– ident: B52
  doi: 10.1038/nature04171
– ident: B55
  doi: 10.3389/fpsyg.2012.00030
– ident: B13
  doi: 10.1016/j.cophys.2020.08.016
– ident: B34
  doi: 10.1371/journal.pone.0052267
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  doi: 10.1523/JNEUROSCI.4031-15.2016
– ident: B56
  doi: 10.1111/ejn.12746
– ident: B32
  doi: 10.1073/pnas.94.20.10979
– ident: B22
  doi: 10.3389/fnhum.2016.00380
– ident: B29
  doi: 10.3758/s13423-011-0055-3
– ident: B28
  doi: 10.3758/bf03208800
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  doi: 10.1007/s00359-008-0340-4
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  doi: 10.1523/JNEUROSCI.4861-13.2014
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  doi: 10.1371/journal.pone.0155991
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  doi: 10.1046/j.1365-2273.2002.00541.x
– ident: B4
  doi: 10.1037/a0037163
– ident: B6
  doi: 10.1016/j.neubiorev.2019.03.017
– ident: B16
  doi: 10.1016/0014-4886(71)90003-3
– ident: B27
  doi: 10.1017/s0140525x01003922
– volume-title: Working Memory Capacity
  year: 2016
  ident: B7
  doi: 10.4324/9781315625560
– ident: B14
  doi: 10.1016/j.neuroscience.2012.07.062
– ident: B20
  doi: 10.1152/physrev.2001.81.3.1305
– ident: B49
  doi: 10.1121/1.414508
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  doi: 10.1111/j.1469-8986.2009.00845.x
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  doi: 10.1016/j.heares.2019.04.010
– ident: B41
  doi: 10.1097/AUD.0b013e31827ada02
– ident: B21
  doi: 10.1152/jn.1997.77.5.2385
– ident: B3
  doi: 10.1038/nn.3655
– ident: B1
  doi: 10.1016/j.neuron.2018.09.023
– ident: B57
  doi: 10.1523/JNEUROSCI.20-12-04701.2000
– ident: B36
  doi: 10.1097/00001756-200003200-00043
– ident: B8
  doi: 10.1016/j.tics.2011.11.014
– ident: B23
  doi: 10.3389/fnhum.2016.00221
– ident: B5
  doi: 10.1037/xhp0000413
– ident: B31
  doi: 10.1016/j.jneumeth.2003.10.009
– ident: B47
  doi: 10.1016/j.heares.2017.02.003
– ident: B25
  doi: 10.1162/jocn_a_00275
– volume: 10
  start-page: 565
  year: 2007
  ident: B39
  publication-title: Dev Sci
  doi: 10.1111/j.1467-7687.2007.00619.x
– ident: B33
  doi: 10.1016/j.jesp.2013.03.013
– ident: B37
  doi: 10.1016/j.neuroimage.2006.07.015
– ident: B50
  doi: 10.1016/0031-9384(95)00012-8
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  doi: 10.1007/s12311-015-0694-4
– volume: 72
  start-page: 296
  year: 2012
  ident: B44
  publication-title: Acta Neurobiol Exp
  doi: 10.55782/ane-2012-1902
– ident: B60
  doi: 10.1186/s12915-021-00992-8
– ident: B30
  doi: 10.1038/349413a0
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  doi: 10.1371/journal.pone.0165645
– ident: B59
  doi: 10.3389/fnsys.2018.00042
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  doi: 10.1093/cercor/bhj035
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  doi: 10.1523/JNEUROSCI.3702-06.2007
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  doi: 10.1371/journal.pone.0208939
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  doi: 10.1016/j.clinph.2003.11.021
– ident: B42
  doi: 10.1016/j.ijpsycho.2014.09.012
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  doi: 10.1007/s11065-012-9202-5
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  doi: 10.1007/s10162-015-0509-9
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  doi: 10.1073/pnas.1523471113
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Snippet The auditory efferent system has been proposed to function as a biological filter of cochlear responses during selective attention. Here, we recorded...
Top-down modulation of sensory responses to distracting stimuli by selective attention has been proposed as an important mechanism by which our brain can...
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SubjectTerms Acoustic Stimulation
Adult
Auditory Perception - physiology
Cochlea - physiology
Cochlear Nucleus - physiology
Efferent Pathways - physiology
Electroencephalography
Evoked Potentials, Auditory - physiology
Female
Hearing - physiology
Humans
Male
Memory, Short-Term - physiology
Reflex - physiology
Superior Olivary Complex - physiology
Visual Perception - physiology
Young Adult
Title The medial olivocochlear reflex strength is modulated during a visual working memory task
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