Cytokines and sleep
Abstract
Personal experience and empirical data indicate sleep is altered during sickness. Important signaling molecules of the peripheral immune system called cytokines orchestrate responses to infection. Through a variety of mechanisms, the brain detects activation of the peripheral immune system. The brain responds to infection by altering physiological processes and complex behavior, including sleep. These changes in physiology and behavior collectively function to support the immune system, and under normal circumstances the health of the host is restored. Several of these cytokines, and their receptors, are present in normal healthy brain. Some cytokines regulate sleep under physiological conditions, in the absence of infection or immune challenge. For example, interleukin-1 directly alters discharge patterns of neurons in hypothalamic and brainstem circuits implicated in the regulation of sleep-wake behavior. Many other cytokines modulate sleep because they interact with neurotransmitter, peptide, and/or hormone systems to initiate a cascade of responses that subsequently alter sleep-wake behavior. Because cytokines regulate/modulate sleep-wake behavior in the absence of immune challenge, and cytokine concentrations and profiles are altered during infection, it is likely that cytokines mediate infection-induced alterations in sleep. Whether the changes in sleep that occur during infection are beneficial and aid in recovery remains to be determined.
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Administration of either IL-1 or TNF promotes NREM sleep.
“Administration of either IL-1 or TNF promotes NREM sleep (Obal and Krueger, 2003;Opp, 2005;Krueger, 2008).”
From Sleep health: Reciprocal regulation of sleep and innate immunity (2017) · cites this paper as Opp, 2005
In humans, DAMPs increase in the brain, CSF, and blood following acute sleep deprivation.
“in humans, DAMPs increase in the brain (509), CSF (410), and blood (35) following acute sleep deprivation.”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [410]
Amyloid beta was found to be lower following a night of regular sleep compared with a night of total sleep deprivation or SWS disruption.
“amyloid beta was found to be lower following a night of regular sleep compared with a night of total sleep deprivation (410, 509) or SWS disruption”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [410]
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References 371 · Cited by 393
- Authors
- Opp, M. R.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Opp, Mark R.
- ORCID
- Opp, Mark R.
- Venue
- Sleep Medicine Reviews
- Publisher
- Elsevier BV
- Published
- 2005-10
- Volume
- 9
- Issue
- 5
- Pages
- 355-364
- ISSN
- 1087-0792 (ISSN-L)
- OpenAlex
- W2047445016
- Cited by
- 393
- References
- 371
- Citations by year
- 2026: 12 · 2025: 17 · 2024: 20 · 2023: 13 · 2022: 20 · 2021: 29 · 2020: 20 · 2019: 17 · 2018: 11 · 2017: 17 · 2016: 25 · 2015: 16 · 2014: 19 · 2013: 27 · 2012: 23
- FWCI
- 1.46
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Sleep Medicine Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical School, University of Michigan
- National Institutes of Health (MH64843)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Keywords
- cytokines, sleep, sleep-wake behavior, infection, immune system, neuroimmune interactions, interleukin-1, hypothalamus, brainstem, sleep regulation, cytokine receptors
- MeSH terms
- Bacterial Infections, Brain Stem, Humans, Hypothalamus, Cytokines, Sleep Disorders, Circadian Rhythm
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