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Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations

This study’s primary objective is to analyze human EEG spindle oscillations during propofol-induced anesthesia and to address possible activation sources. Such an analysis also has a secondary role of investigating the short- term spectral patterns and their functional role. Artifact-free epochs of...

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Autores principales: Ozgoren, Murat, Bayazit, Onur, Gokmen, Necati, Oniz, Adile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141347/
https://www.ncbi.nlm.nih.gov/pubmed/21792383
http://dx.doi.org/10.2174/1874440001004010121
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author Ozgoren, Murat
Bayazit, Onur
Gokmen, Necati
Oniz, Adile
author_facet Ozgoren, Murat
Bayazit, Onur
Gokmen, Necati
Oniz, Adile
author_sort Ozgoren, Murat
collection PubMed
description This study’s primary objective is to analyze human EEG spindle oscillations during propofol-induced anesthesia and to address possible activation sources. Such an analysis also has a secondary role of investigating the short- term spectral patterns and their functional role. Artifact-free epochs of spindle activations were selected from the electroencephalograms of patients undergoing propofol anesthesia. Power spectral analysis and source localization using standardized low-resolution-brain-electromagnetic-tomography (sLORETA) were performed. Additionally, spectrograms were obtained by means of using the Complex Morlet-based algorithm. In order to highlight the functional properties, auditory stimulations were conducted during the propofol administration. The loss of consciousness was reached at a level of 0.8-1.2 µg/mL, which also provided distinct spindle oscillations in the continuous EEG. The un-evoked (spontaneous) and evoked (auditory) conditions were examined across non-medicated and medicated conditions (propofol). The propofol administration resulted in appearance of 12-14 Hz spindle activity mostly localized in BA6, BA9, BA10, BA21, BA24 and BA37 areas. The presence of auditory stimulations slightly shifted these maximum activities to different locations. Between the medicated and non-medicated conditions, there was a significant reduction of spindle activity, which was pinpointed to BA7 (precuneus area). The findings indicate that spindle oscillations may have a dual nature. That is, spindle oscillations may be activity dependent and disruptive for large-scale information processing networks in the brain. Hence, the study of spindle oscillation may provide a basis for understanding the short-term spectral patterns of human EEG.
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spelling pubmed-31413472011-07-26 Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations Ozgoren, Murat Bayazit, Onur Gokmen, Necati Oniz, Adile Open Neuroimag J Article This study’s primary objective is to analyze human EEG spindle oscillations during propofol-induced anesthesia and to address possible activation sources. Such an analysis also has a secondary role of investigating the short- term spectral patterns and their functional role. Artifact-free epochs of spindle activations were selected from the electroencephalograms of patients undergoing propofol anesthesia. Power spectral analysis and source localization using standardized low-resolution-brain-electromagnetic-tomography (sLORETA) were performed. Additionally, spectrograms were obtained by means of using the Complex Morlet-based algorithm. In order to highlight the functional properties, auditory stimulations were conducted during the propofol administration. The loss of consciousness was reached at a level of 0.8-1.2 µg/mL, which also provided distinct spindle oscillations in the continuous EEG. The un-evoked (spontaneous) and evoked (auditory) conditions were examined across non-medicated and medicated conditions (propofol). The propofol administration resulted in appearance of 12-14 Hz spindle activity mostly localized in BA6, BA9, BA10, BA21, BA24 and BA37 areas. The presence of auditory stimulations slightly shifted these maximum activities to different locations. Between the medicated and non-medicated conditions, there was a significant reduction of spindle activity, which was pinpointed to BA7 (precuneus area). The findings indicate that spindle oscillations may have a dual nature. That is, spindle oscillations may be activity dependent and disruptive for large-scale information processing networks in the brain. Hence, the study of spindle oscillation may provide a basis for understanding the short-term spectral patterns of human EEG. Bentham Open 2010-09-08 /pmc/articles/PMC3141347/ /pubmed/21792383 http://dx.doi.org/10.2174/1874440001004010121 Text en © Ozgoren et al.; Licensee Bentham Open. http://creativecommons.org/-licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/-licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Ozgoren, Murat
Bayazit, Onur
Gokmen, Necati
Oniz, Adile
Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations
title Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations
title_full Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations
title_fullStr Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations
title_full_unstemmed Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations
title_short Spectral Pattern Analysis of Propofol Induced Spindle Oscillations in the Presence of Auditory Stimulations
title_sort spectral pattern analysis of propofol induced spindle oscillations in the presence of auditory stimulations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141347/
https://www.ncbi.nlm.nih.gov/pubmed/21792383
http://dx.doi.org/10.2174/1874440001004010121
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