Cited by 74Systemic Lupus Erythematosus ResearchSleep and Wakefulness ResearchSleep and Work-Related Fatigue

Effects of sleep deprivation on the development of autoimmune disease in an experimental model of systemic lupus erythematosus

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Palma, Beatriz Duarte, Gabriel, Alexandre, Colugnati, Fernando A. B., Tufik, Sergio·2006·American Journal of Physiology-Regulatory, Integrative and Comparative Physiology

Abstract

Sleep is hypothesized to play a restorative role on immune system. In addition, disturbed sleep is thought to impair host defense mechanisms. Chronic sleep deprivation is a common occurrence in modern society and has been observed in a number of chronic inflammatory conditions, such as systemic lupus erythematosus (SLE). New Zealand Black/New Zealand White (NZB/NZW) F 1 mice develop an autoimmune disease that strongly resembles SLE in humans, exhibiting high titers of antinuclear antibodies associated with the development of rapidly progressive and lethal glomerulonephritis. On the basis of this evidence, the present study examined the onset and progress of lupus in as-yet healthy female mice submitted to sleep deprivation. Sleep deprivation was accomplished by two 96-h periods in the multiple-platform method when mice were 10 wk old, and they were observed until 28 wk of age. Blood samples were collected from the orbital plexus fortnightly to evaluate serum antinuclear antibodies and anti-double-stranded DNA. Proteinuria and longevity as well as body weight were also assessed. The results indicated that mice submitted to sleep deprivation exhibited an earlier onset of the disease, as reflected by the increased number of antinuclear antibodies. However, no statistical difference was found in the other parameters analyzed. According to these results, sleep deprivation could be considered as a risk factor for the onset but not for the evolution of the disease.

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Crossref · 10.1152/ajpregu.00186.2006

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66 of 66 references verified0 citation errors · 0 not checkable

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  • Some reports show increased numbers of lymphocyte subsets (CD4 T cells, CD8 T cells, and NK cells), particularly when measured in the evening after a regular night of sleep.

    “However, there are some reports of increased numbers of lymphocyte subsets (i.e., CD4 T cells, CD8 T cells, and NK cells), particularly when measured in the evening after a regular night of sleep (152, 234, 418, 556, 580).”

    From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [418]

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Authors
Palma, B. D., Gabriel, A., Colugnati, F. A. B., & Tufik, S.
Affiliations
Universidade Federal de São Paulo (BR)
Venue
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Published
2006-11
Volume
291
Issue
5
Pages
R1527-R1532
ISSN
  • 0363-6119 (ISSN-L)
  • 1522-1490
OpenAlex
W2128745305
Cited by
74
References
65
Citations by year
2026: 3 · 2025: 4 · 2024: 4 · 2023: 3 · 2022: 12 · 2021: 4 · 2020: 7 · 2019: 5 · 2018: 5 · 2017: 4 · 2016: 1 · 2015: 4 · 2014: 2 · 2013: 2 · 2012: 2
FWCI
1.31
Type
journal article
Language
en
Open access
Licence
other-oa
Locations
  • American Journal of Physiology-Regulatory, Integrative and Comparative Physiology (publishedVersion)
  • PubMed (publishedVersion)
  • Americanae (AECID Library) (submittedVersion, other-oa)
  • LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, other-oa)
Funders
Fundação de Amparo à Pesquisa do Estado de São Paulo
Topics
  • Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
Keywords
sleep deprivation, systemic lupus erythematosus, NZB/W F1 mice, autoimmune disease onset, antinuclear antibodies, anti-dsDNA antibodies, glomerulonephritis, proteinuria, longevity, sleep disorders, risk factors
MeSH terms
Animals, Antibodies, Antinuclear, Autoimmune Diseases, Body Weight, Disease Models, Animal, Female, Longevity, Lupus Erythematosus, Systemic, Male, Mice, Inbred NZB, Mice, Inbred Strains, Proteinuria, Risk Factors, Sleep Deprivation, Disease Progression, Mice

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