The influence of sleep deprivation and obesity on DNA damage in female Zucker rats

Detalhes bibliográficos
Autor(a) principal: Tenorio, Neuli M.
Data de Publicação: 2013
Outros Autores: Ribeiro, Daniel A., Alvarenga, Tathiana A., Fracalossi, Ana Carolina C., Carlin, Viviane, Hirotsu, Camila, Tufik, Sergio, Andersen, Monica L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/72138
Resumo: OBJECTIVE: The aim of this study was to evaluate overall genetic damage induced by total sleep deprivation in obese, female Zucker rats of differing ages. METHOD: Lean and obese Zucker rats at 3, 6, and 15 months old were randomly distributed into two groups for each age group: home-cage control and sleep-deprived (N = 5/group). The sleep-deprived groups were deprived sleep by gentle handling for 6 hours, whereas the home-cage control group was allowed to remain undisturbed in their home-cage. At the end of the sleep deprivation period, or after an equivalent amount of time for the home-cage control groups, the rats were brought to an adjacent room and decapitated. The blood, brain, and liver tissue were collected and stored individually to evaluate DNA damage. RESULTS: Significant genetic damage was observed only in 15-month-old rats. Genetic damage was present in the liver cells from sleep-deprived obese rats compared with lean rats in the same condition. Sleep deprivation was associated with genetic damage in brain cells regardless of obesity status. DNA damage was observed in the peripheral blood cells regardless of sleep condition or obesity status. CONCLUSION: Taken together, these results suggest that obesity was associated with genetic damage in liver cells, whereas sleep deprivation was associated with DNA damage in brain cells. These results also indicate that there is no synergistic effect of these noxious conditions on the overall level of genetic damage. In addition, the level of DNA damage was significantly higher in 15-month-old rats compared to younger rats.
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spelling The influence of sleep deprivation and obesity on DNA damage in female Zucker ratsSleep DeprivationObesityZucker RatsDNA DamageComet AssayGentle HandlingFemaleOBJECTIVE: The aim of this study was to evaluate overall genetic damage induced by total sleep deprivation in obese, female Zucker rats of differing ages. METHOD: Lean and obese Zucker rats at 3, 6, and 15 months old were randomly distributed into two groups for each age group: home-cage control and sleep-deprived (N = 5/group). The sleep-deprived groups were deprived sleep by gentle handling for 6 hours, whereas the home-cage control group was allowed to remain undisturbed in their home-cage. At the end of the sleep deprivation period, or after an equivalent amount of time for the home-cage control groups, the rats were brought to an adjacent room and decapitated. The blood, brain, and liver tissue were collected and stored individually to evaluate DNA damage. RESULTS: Significant genetic damage was observed only in 15-month-old rats. Genetic damage was present in the liver cells from sleep-deprived obese rats compared with lean rats in the same condition. Sleep deprivation was associated with genetic damage in brain cells regardless of obesity status. DNA damage was observed in the peripheral blood cells regardless of sleep condition or obesity status. CONCLUSION: Taken together, these results suggest that obesity was associated with genetic damage in liver cells, whereas sleep deprivation was associated with DNA damage in brain cells. These results also indicate that there is no synergistic effect of these noxious conditions on the overall level of genetic damage. In addition, the level of DNA damage was significantly higher in 15-month-old rats compared to younger rats.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2013-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/7213810.1590/clin.v68i3.72138Clinics; Vol. 68 No. 3 (2013); 385-389Clinics; v. 68 n. 3 (2013); 385-389Clinics; Vol. 68 Núm. 3 (2013); 385-3891980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/72138/75373Tenorio, Neuli M.Ribeiro, Daniel A.Alvarenga, Tathiana A.Fracalossi, Ana Carolina C.Carlin, VivianeHirotsu, CamilaTufik, SergioAndersen, Monica L.info:eu-repo/semantics/openAccess2014-01-28T17:05:37Zoai:revistas.usp.br:article/72138Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2014-01-28T17:05:37Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
title The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
spellingShingle The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
Tenorio, Neuli M.
Sleep Deprivation
Obesity
Zucker Rats
DNA Damage
Comet Assay
Gentle Handling
Female
title_short The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
title_full The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
title_fullStr The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
title_full_unstemmed The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
title_sort The influence of sleep deprivation and obesity on DNA damage in female Zucker rats
author Tenorio, Neuli M.
author_facet Tenorio, Neuli M.
Ribeiro, Daniel A.
Alvarenga, Tathiana A.
Fracalossi, Ana Carolina C.
Carlin, Viviane
Hirotsu, Camila
Tufik, Sergio
Andersen, Monica L.
author_role author
author2 Ribeiro, Daniel A.
Alvarenga, Tathiana A.
Fracalossi, Ana Carolina C.
Carlin, Viviane
Hirotsu, Camila
Tufik, Sergio
Andersen, Monica L.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Tenorio, Neuli M.
Ribeiro, Daniel A.
Alvarenga, Tathiana A.
Fracalossi, Ana Carolina C.
Carlin, Viviane
Hirotsu, Camila
Tufik, Sergio
Andersen, Monica L.
dc.subject.por.fl_str_mv Sleep Deprivation
Obesity
Zucker Rats
DNA Damage
Comet Assay
Gentle Handling
Female
topic Sleep Deprivation
Obesity
Zucker Rats
DNA Damage
Comet Assay
Gentle Handling
Female
description OBJECTIVE: The aim of this study was to evaluate overall genetic damage induced by total sleep deprivation in obese, female Zucker rats of differing ages. METHOD: Lean and obese Zucker rats at 3, 6, and 15 months old were randomly distributed into two groups for each age group: home-cage control and sleep-deprived (N = 5/group). The sleep-deprived groups were deprived sleep by gentle handling for 6 hours, whereas the home-cage control group was allowed to remain undisturbed in their home-cage. At the end of the sleep deprivation period, or after an equivalent amount of time for the home-cage control groups, the rats were brought to an adjacent room and decapitated. The blood, brain, and liver tissue were collected and stored individually to evaluate DNA damage. RESULTS: Significant genetic damage was observed only in 15-month-old rats. Genetic damage was present in the liver cells from sleep-deprived obese rats compared with lean rats in the same condition. Sleep deprivation was associated with genetic damage in brain cells regardless of obesity status. DNA damage was observed in the peripheral blood cells regardless of sleep condition or obesity status. CONCLUSION: Taken together, these results suggest that obesity was associated with genetic damage in liver cells, whereas sleep deprivation was associated with DNA damage in brain cells. These results also indicate that there is no synergistic effect of these noxious conditions on the overall level of genetic damage. In addition, the level of DNA damage was significantly higher in 15-month-old rats compared to younger rats.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/72138
10.1590/clin.v68i3.72138
url https://www.revistas.usp.br/clinics/article/view/72138
identifier_str_mv 10.1590/clin.v68i3.72138
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/72138/75373
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 68 No. 3 (2013); 385-389
Clinics; v. 68 n. 3 (2013); 385-389
Clinics; Vol. 68 Núm. 3 (2013); 385-389
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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