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Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice

OBJECTIVE: This study aimed to explore the relationship among several indices of circadian rhythms and lipid peroxidation of brain tissue in mice. METHODS: After entrainment of 4-week-old mice, one group was disrupted their circadian rhythms for three days and the other group for seven days (n = 10,...

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Autores principales: Oh, Chi Eun, Lim, Hyun Ju, Park, Jeounghyun, Moon, Eunsoo, Park, Ji Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606440/
https://www.ncbi.nlm.nih.gov/pubmed/36263640
http://dx.doi.org/10.9758/cpn.2022.20.4.649
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author Oh, Chi Eun
Lim, Hyun Ju
Park, Jeounghyun
Moon, Eunsoo
Park, Ji Kyoung
author_facet Oh, Chi Eun
Lim, Hyun Ju
Park, Jeounghyun
Moon, Eunsoo
Park, Ji Kyoung
author_sort Oh, Chi Eun
collection PubMed
description OBJECTIVE: This study aimed to explore the relationship among several indices of circadian rhythms and lipid peroxidation of brain tissue in mice. METHODS: After entrainment of 4-week-old mice, one group was disrupted their circadian rhythms for three days and the other group for seven days (n = 10, respectively). After a recovery period, the Y-maze test, the elevated plus maze test, the tail suspension test, and the forced swimming test were conducted. To assess lipid peroxidation in brain tissue, thiobarbituric acid reactive substances were measured in the cortex, hippocampus, and cerebellum. RESULTS: When circadian rhythms were disrupted and adapted back to their original rhythm, the recovery time of the 7-day disruption group (median 3.35 days) was significiantly faster than one of the 3-day disruption group (median 4.87 days). In the group with a 7-day disruption, mice that had recovered their rhythms early had higher malondialdehyde levels in their hippocampus compared to those with delayed recovery. The entrainment of circadian rhythms was negatively correlated with the malondialdehyde level of brain tissue. The behavioral test results showed no differences depending on the disruption durations or recovery patterns of circadian rhythms. CONCLUSION: These results suggest that disruption types, recovery patterns, and the entrainment of circadian rhythms are likely to affect oxidative stress in adolescents or young adult mice. Future study is needed to confirm and specify these results on the effects of circadian rhythms on oxidative stress and age-dependent effects.
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spelling pubmed-96064402022-11-30 Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice Oh, Chi Eun Lim, Hyun Ju Park, Jeounghyun Moon, Eunsoo Park, Ji Kyoung Clin Psychopharmacol Neurosci Original Article OBJECTIVE: This study aimed to explore the relationship among several indices of circadian rhythms and lipid peroxidation of brain tissue in mice. METHODS: After entrainment of 4-week-old mice, one group was disrupted their circadian rhythms for three days and the other group for seven days (n = 10, respectively). After a recovery period, the Y-maze test, the elevated plus maze test, the tail suspension test, and the forced swimming test were conducted. To assess lipid peroxidation in brain tissue, thiobarbituric acid reactive substances were measured in the cortex, hippocampus, and cerebellum. RESULTS: When circadian rhythms were disrupted and adapted back to their original rhythm, the recovery time of the 7-day disruption group (median 3.35 days) was significiantly faster than one of the 3-day disruption group (median 4.87 days). In the group with a 7-day disruption, mice that had recovered their rhythms early had higher malondialdehyde levels in their hippocampus compared to those with delayed recovery. The entrainment of circadian rhythms was negatively correlated with the malondialdehyde level of brain tissue. The behavioral test results showed no differences depending on the disruption durations or recovery patterns of circadian rhythms. CONCLUSION: These results suggest that disruption types, recovery patterns, and the entrainment of circadian rhythms are likely to affect oxidative stress in adolescents or young adult mice. Future study is needed to confirm and specify these results on the effects of circadian rhythms on oxidative stress and age-dependent effects. Korean College of Neuropsychopharmacology 2022-11-30 2022-11-30 /pmc/articles/PMC9606440/ /pubmed/36263640 http://dx.doi.org/10.9758/cpn.2022.20.4.649 Text en Copyright© 2022, Korean College of Neuropsychopharmacology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Oh, Chi Eun
Lim, Hyun Ju
Park, Jeounghyun
Moon, Eunsoo
Park, Ji Kyoung
Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice
title Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice
title_full Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice
title_fullStr Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice
title_full_unstemmed Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice
title_short Relationship of Circadian Rhythm in Behavioral Characteristics and Lipid Peroxidation of Brain Tissues in Mice
title_sort relationship of circadian rhythm in behavioral characteristics and lipid peroxidation of brain tissues in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606440/
https://www.ncbi.nlm.nih.gov/pubmed/36263640
http://dx.doi.org/10.9758/cpn.2022.20.4.649
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