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On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise

The spectral analysis of the spontaneous activity recorded with an electrode positioned near the round window of the guinea pig cochlea shows a broad energy peak between 800 and 1,000 Hz. This spontaneous electric activity is called round window noise or ensemble background activity. In guinea pigs,...

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Autores principales: Pardo-Jadue, Javiera, Dragicevic, Constantino D., Bowen, Macarena, Delano, Paul H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504225/
https://www.ncbi.nlm.nih.gov/pubmed/28744193
http://dx.doi.org/10.3389/fnins.2017.00395
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author Pardo-Jadue, Javiera
Dragicevic, Constantino D.
Bowen, Macarena
Delano, Paul H.
author_facet Pardo-Jadue, Javiera
Dragicevic, Constantino D.
Bowen, Macarena
Delano, Paul H.
author_sort Pardo-Jadue, Javiera
collection PubMed
description The spectral analysis of the spontaneous activity recorded with an electrode positioned near the round window of the guinea pig cochlea shows a broad energy peak between 800 and 1,000 Hz. This spontaneous electric activity is called round window noise or ensemble background activity. In guinea pigs, the proposed origin of this peak is the random sum of the extracellular field potentials generated by action potentials of auditory nerve neurons. In this study, we used a non-invasive method to record the tympanic electric noise (TEN) in humans by means of a tympanic wick electrode. We recorded a total of 24 volunteers, under silent conditions or in response to stimuli of different modalities, including auditory, vestibular, and motor activity. Our results show a reliable peak of spontaneous activity at ~1,000 Hz in all studied subjects. In addition, we found stimulus-driven responses with broad-band noise that in most subjects produced an increase in the magnitude of the energy band around 1,000 Hz (between 650 and 1,200 Hz). Our results with the vestibular stimulation were not conclusive, as we found responses with all caloric stimuli, including 37°C. No responses were observed with motor tasks, like eye movements or blinking. We demonstrate the feasibility of recording neural activity from the electric noise of the tympanic membrane with a non-invasive method. From our results, we suggest that the 1,000 Hz component of the TEN has a mixed origin including peripheral and central auditory pathways. This research opens up the possibility of future clinical non-invasive techniques for the functional study of auditory and vestibular nerves in humans.
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spelling pubmed-55042252017-07-25 On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise Pardo-Jadue, Javiera Dragicevic, Constantino D. Bowen, Macarena Delano, Paul H. Front Neurosci Neuroscience The spectral analysis of the spontaneous activity recorded with an electrode positioned near the round window of the guinea pig cochlea shows a broad energy peak between 800 and 1,000 Hz. This spontaneous electric activity is called round window noise or ensemble background activity. In guinea pigs, the proposed origin of this peak is the random sum of the extracellular field potentials generated by action potentials of auditory nerve neurons. In this study, we used a non-invasive method to record the tympanic electric noise (TEN) in humans by means of a tympanic wick electrode. We recorded a total of 24 volunteers, under silent conditions or in response to stimuli of different modalities, including auditory, vestibular, and motor activity. Our results show a reliable peak of spontaneous activity at ~1,000 Hz in all studied subjects. In addition, we found stimulus-driven responses with broad-band noise that in most subjects produced an increase in the magnitude of the energy band around 1,000 Hz (between 650 and 1,200 Hz). Our results with the vestibular stimulation were not conclusive, as we found responses with all caloric stimuli, including 37°C. No responses were observed with motor tasks, like eye movements or blinking. We demonstrate the feasibility of recording neural activity from the electric noise of the tympanic membrane with a non-invasive method. From our results, we suggest that the 1,000 Hz component of the TEN has a mixed origin including peripheral and central auditory pathways. This research opens up the possibility of future clinical non-invasive techniques for the functional study of auditory and vestibular nerves in humans. Frontiers Media S.A. 2017-07-11 /pmc/articles/PMC5504225/ /pubmed/28744193 http://dx.doi.org/10.3389/fnins.2017.00395 Text en Copyright © 2017 Pardo-Jadue, Dragicevic, Bowen and Delano. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Pardo-Jadue, Javiera
Dragicevic, Constantino D.
Bowen, Macarena
Delano, Paul H.
On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise
title On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise
title_full On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise
title_fullStr On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise
title_full_unstemmed On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise
title_short On the Origin of the 1,000 Hz Peak in the Spectrum of the Human Tympanic Electrical Noise
title_sort on the origin of the 1,000 hz peak in the spectrum of the human tympanic electrical noise
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504225/
https://www.ncbi.nlm.nih.gov/pubmed/28744193
http://dx.doi.org/10.3389/fnins.2017.00395
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