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Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition
The auditory evoked startle reflex is a conserved response resulting in neurological and motor activity. The presence of a mild prepulse immediately before the main pulse inhibits startle responses, though the mechanism for this remains unknown. In this study, the electroencephalography (EEG) data r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593922/ https://www.ncbi.nlm.nih.gov/pubmed/28894145 http://dx.doi.org/10.1038/s41598-017-11191-3 |
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author | Potter, Thomas Li, Sheng Nguyen, Thinh Nguyen, Trac Ince, Nuri Zhang, Yingchun |
author_facet | Potter, Thomas Li, Sheng Nguyen, Thinh Nguyen, Trac Ince, Nuri Zhang, Yingchun |
author_sort | Potter, Thomas |
collection | PubMed |
description | The auditory evoked startle reflex is a conserved response resulting in neurological and motor activity. The presence of a mild prepulse immediately before the main pulse inhibits startle responses, though the mechanism for this remains unknown. In this study, the electroencephalography (EEG) data recorded from 15 subjects was analyzed to study the N1 and P2 components of cortical auditory evoked potentials (CAEPs) evoked by 70, 80, 90, 100, and 110 dB stimuli both in the presence and absence of 70 dB prepulses. Results without a prepulse showed an evolution of N1 amplitudes, increasing with stimulus intensity and showing largely significant differences. Results from prepulse trials only showed noteworthy changes in peak-to-peak amplitude in the 100 dB condition. Prepulse and non-prepulse conditions were then compared using peak amplitudes and theta power. Prepulse conditions significantly decreased the amplitude for both components in the 110 dB condition, i.e., pre-pulse inhibition, but significantly increased the N1 amplitude in the 70 dB condition, i.e., pre-pulse facilitation. Similarly theta band power significantly increased in the 70 dB prepulse condition and significantly decreased in the 110 dB prepulse condition. These results expand the basis of knowledge regarding how CAEPs change and elaborate on their neural function and representation. |
format | Online Article Text |
id | pubmed-5593922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55939222017-09-13 Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition Potter, Thomas Li, Sheng Nguyen, Thinh Nguyen, Trac Ince, Nuri Zhang, Yingchun Sci Rep Article The auditory evoked startle reflex is a conserved response resulting in neurological and motor activity. The presence of a mild prepulse immediately before the main pulse inhibits startle responses, though the mechanism for this remains unknown. In this study, the electroencephalography (EEG) data recorded from 15 subjects was analyzed to study the N1 and P2 components of cortical auditory evoked potentials (CAEPs) evoked by 70, 80, 90, 100, and 110 dB stimuli both in the presence and absence of 70 dB prepulses. Results without a prepulse showed an evolution of N1 amplitudes, increasing with stimulus intensity and showing largely significant differences. Results from prepulse trials only showed noteworthy changes in peak-to-peak amplitude in the 100 dB condition. Prepulse and non-prepulse conditions were then compared using peak amplitudes and theta power. Prepulse conditions significantly decreased the amplitude for both components in the 110 dB condition, i.e., pre-pulse inhibition, but significantly increased the N1 amplitude in the 70 dB condition, i.e., pre-pulse facilitation. Similarly theta band power significantly increased in the 70 dB prepulse condition and significantly decreased in the 110 dB prepulse condition. These results expand the basis of knowledge regarding how CAEPs change and elaborate on their neural function and representation. Nature Publishing Group UK 2017-09-11 /pmc/articles/PMC5593922/ /pubmed/28894145 http://dx.doi.org/10.1038/s41598-017-11191-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Potter, Thomas Li, Sheng Nguyen, Thinh Nguyen, Trac Ince, Nuri Zhang, Yingchun Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition |
title | Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition |
title_full | Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition |
title_fullStr | Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition |
title_full_unstemmed | Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition |
title_short | Characterization of Volume-Based Changes in Cortical Auditory Evoked Potentials and Prepulse Inhibition |
title_sort | characterization of volume-based changes in cortical auditory evoked potentials and prepulse inhibition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593922/ https://www.ncbi.nlm.nih.gov/pubmed/28894145 http://dx.doi.org/10.1038/s41598-017-11191-3 |
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