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Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage

Transgenic modification of the two most common genes (APPsw, PS1ΔE9) related to familial Alzheimer’s disease (AD) in rats has produced a rodent model that develops pathognomonic signs of AD without genetic tau-protein modification. We used 17-month-old AD rats (n = 8) and age-matched controls (AC, n...

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Autores principales: Kreuzer, Matthias, Keating, Glenda L., Fenzl, Thomas, Härtner, Lorenz, Sinon, Christopher G., Hajjar, Ihab, Ciavatta, Vincent, Rye, David B., García, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730237/
https://www.ncbi.nlm.nih.gov/pubmed/33291462
http://dx.doi.org/10.3390/ijms21239290
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author Kreuzer, Matthias
Keating, Glenda L.
Fenzl, Thomas
Härtner, Lorenz
Sinon, Christopher G.
Hajjar, Ihab
Ciavatta, Vincent
Rye, David B.
García, Paul S.
author_facet Kreuzer, Matthias
Keating, Glenda L.
Fenzl, Thomas
Härtner, Lorenz
Sinon, Christopher G.
Hajjar, Ihab
Ciavatta, Vincent
Rye, David B.
García, Paul S.
author_sort Kreuzer, Matthias
collection PubMed
description Transgenic modification of the two most common genes (APPsw, PS1ΔE9) related to familial Alzheimer’s disease (AD) in rats has produced a rodent model that develops pathognomonic signs of AD without genetic tau-protein modification. We used 17-month-old AD rats (n = 8) and age-matched controls (AC, n = 7) to evaluate differences in sleep behavior and EEG features during wakefulness (WAKE), non-rapid eye movement sleep (NREM), and rapid eye movement sleep (REM) over 24-h EEG recording (12:12h dark–light cycle). We discovered that AD rats had more sleep–wake transitions and an increased probability of shorter REM and NREM bouts. AD rats also expressed a more uniform distribution of the relative spectral power. Through analysis of information content in the EEG using entropy of difference, AD animals demonstrated less EEG information during WAKE, but more information during NREM. This seems to indicate a limited range of changes in EEG activity that could be caused by an AD-induced change in inhibitory network function as reflected by increased GABAAR-β2 expression but no increase in GAD-67 in AD animals. In conclusion, this transgenic rat model of Alzheimer’s disease demonstrates less obvious EEG features of WAKE during wakefulness and less canonical features of sleep during sleep.
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spelling pubmed-77302372020-12-12 Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage Kreuzer, Matthias Keating, Glenda L. Fenzl, Thomas Härtner, Lorenz Sinon, Christopher G. Hajjar, Ihab Ciavatta, Vincent Rye, David B. García, Paul S. Int J Mol Sci Article Transgenic modification of the two most common genes (APPsw, PS1ΔE9) related to familial Alzheimer’s disease (AD) in rats has produced a rodent model that develops pathognomonic signs of AD without genetic tau-protein modification. We used 17-month-old AD rats (n = 8) and age-matched controls (AC, n = 7) to evaluate differences in sleep behavior and EEG features during wakefulness (WAKE), non-rapid eye movement sleep (NREM), and rapid eye movement sleep (REM) over 24-h EEG recording (12:12h dark–light cycle). We discovered that AD rats had more sleep–wake transitions and an increased probability of shorter REM and NREM bouts. AD rats also expressed a more uniform distribution of the relative spectral power. Through analysis of information content in the EEG using entropy of difference, AD animals demonstrated less EEG information during WAKE, but more information during NREM. This seems to indicate a limited range of changes in EEG activity that could be caused by an AD-induced change in inhibitory network function as reflected by increased GABAAR-β2 expression but no increase in GAD-67 in AD animals. In conclusion, this transgenic rat model of Alzheimer’s disease demonstrates less obvious EEG features of WAKE during wakefulness and less canonical features of sleep during sleep. MDPI 2020-12-05 /pmc/articles/PMC7730237/ /pubmed/33291462 http://dx.doi.org/10.3390/ijms21239290 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kreuzer, Matthias
Keating, Glenda L.
Fenzl, Thomas
Härtner, Lorenz
Sinon, Christopher G.
Hajjar, Ihab
Ciavatta, Vincent
Rye, David B.
García, Paul S.
Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage
title Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage
title_full Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage
title_fullStr Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage
title_full_unstemmed Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage
title_short Sleep/Wake Behavior and EEG Signatures of the TgF344-AD Rat Model at the Prodromal Stage
title_sort sleep/wake behavior and eeg signatures of the tgf344-ad rat model at the prodromal stage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730237/
https://www.ncbi.nlm.nih.gov/pubmed/33291462
http://dx.doi.org/10.3390/ijms21239290
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