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General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion

Following general anaesthesia (GA), patients frequently experience sleep disruption and fatigue, which has been hypothesized to result at least in part by GA affecting the circadian clock. Here, we provide the first comprehensive time-dependent analysis of the effects of the commonly administered in...

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Autores principales: Ludin, Nicola M., Orts-Sebastian, Alma, Cheeseman, James F., Chong, Janelle, Merry, Alan F., Cumin, David, Yamazaki, Shin, Pawley, Matthew D. M., Warman, Guy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930986/
https://www.ncbi.nlm.nih.gov/pubmed/33530488
http://dx.doi.org/10.3390/clockssleep3010006
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author Ludin, Nicola M.
Orts-Sebastian, Alma
Cheeseman, James F.
Chong, Janelle
Merry, Alan F.
Cumin, David
Yamazaki, Shin
Pawley, Matthew D. M.
Warman, Guy R.
author_facet Ludin, Nicola M.
Orts-Sebastian, Alma
Cheeseman, James F.
Chong, Janelle
Merry, Alan F.
Cumin, David
Yamazaki, Shin
Pawley, Matthew D. M.
Warman, Guy R.
author_sort Ludin, Nicola M.
collection PubMed
description Following general anaesthesia (GA), patients frequently experience sleep disruption and fatigue, which has been hypothesized to result at least in part by GA affecting the circadian clock. Here, we provide the first comprehensive time-dependent analysis of the effects of the commonly administered inhalational anaesthetic, isoflurane, on the murine circadian clock, by analysing its effects on (a) behavioural locomotor rhythms and (b) PER2::LUC expression in the suprachiasmatic nuclei (SCN) of the mouse brain. Behavioural phase shifts elicited by exposure of mice (n = 80) to six hours of GA (2% isoflurane) were determined by recording wheel-running rhythms in constant conditions (DD). Phase shifts in PER2::LUC expression were determined by recording bioluminescence in organotypic SCN slices (n = 38) prior to and following GA exposure (2% isoflurane). Full phase response curves for the effects of GA on behaviour and PER2::LUC rhythms were constructed, which show that the effects of GA are highly time-dependent. Shifts in SCN PER2 expression were much larger than those of behaviour (c. 0.7 h behaviour vs. 7.5 h PER2::LUC). We discuss the implications of this work for understanding how GA affects the clock, and how it may inform the development of chronotherapeutic strategies to reduce GA-induced phase-shifting in patients.
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spelling pubmed-79309862021-03-05 General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion Ludin, Nicola M. Orts-Sebastian, Alma Cheeseman, James F. Chong, Janelle Merry, Alan F. Cumin, David Yamazaki, Shin Pawley, Matthew D. M. Warman, Guy R. Clocks Sleep Article Following general anaesthesia (GA), patients frequently experience sleep disruption and fatigue, which has been hypothesized to result at least in part by GA affecting the circadian clock. Here, we provide the first comprehensive time-dependent analysis of the effects of the commonly administered inhalational anaesthetic, isoflurane, on the murine circadian clock, by analysing its effects on (a) behavioural locomotor rhythms and (b) PER2::LUC expression in the suprachiasmatic nuclei (SCN) of the mouse brain. Behavioural phase shifts elicited by exposure of mice (n = 80) to six hours of GA (2% isoflurane) were determined by recording wheel-running rhythms in constant conditions (DD). Phase shifts in PER2::LUC expression were determined by recording bioluminescence in organotypic SCN slices (n = 38) prior to and following GA exposure (2% isoflurane). Full phase response curves for the effects of GA on behaviour and PER2::LUC rhythms were constructed, which show that the effects of GA are highly time-dependent. Shifts in SCN PER2 expression were much larger than those of behaviour (c. 0.7 h behaviour vs. 7.5 h PER2::LUC). We discuss the implications of this work for understanding how GA affects the clock, and how it may inform the development of chronotherapeutic strategies to reduce GA-induced phase-shifting in patients. MDPI 2021-01-26 /pmc/articles/PMC7930986/ /pubmed/33530488 http://dx.doi.org/10.3390/clockssleep3010006 Text en © 2021 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
Ludin, Nicola M.
Orts-Sebastian, Alma
Cheeseman, James F.
Chong, Janelle
Merry, Alan F.
Cumin, David
Yamazaki, Shin
Pawley, Matthew D. M.
Warman, Guy R.
General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion
title General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion
title_full General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion
title_fullStr General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion
title_full_unstemmed General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion
title_short General Anaesthesia Shifts the Murine Circadian Clock in a Time-Dependant Fashion
title_sort general anaesthesia shifts the murine circadian clock in a time-dependant fashion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930986/
https://www.ncbi.nlm.nih.gov/pubmed/33530488
http://dx.doi.org/10.3390/clockssleep3010006
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