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Circadian disruption and metabolic disease: Findings from animal models
Open accessAbstract
Social opportunities and work demands have caused humans to become increasingly active during the late evening hours, leading to a shift from the predominantly diurnal lifestyle of our ancestors to a more nocturnal one. This voluntarily decision to stay awake long into the evening hours leads to circadian disruption at the system, tissue, and cellular levels. These derangements are in turn associated with clinical impairments in metabolic processes and physiology. The use of animal models for circadian disruption provides an important opportunity to determine mechanisms by which disorganization in the circadian system can lead to metabolic dysfunction in response to genetic, environmental, and behavioral perturbations. Here we review recent key animal studies involving circadian disruption and discuss the possible translational implications of these studies for human health and particularly for the development of metabolic disease.
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“A major finding to link chrono-disruption and metabolic homeostasis at the molecular level was the discovery of a specific 24-h circadian rhythmicity in adipose tissue genes in 2005 (49,50) .”
From Meal irregularity and cardiometabolic consequences: results from observational and intervention studies (2016) · cites this paper as [50]
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Metadata
- Authors
- Arble, D. M., Ramsey, K. M., Bass, J., & Turek, F. W.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Turek, Fred W.
- Venue
- Best Practice & Research Clinical Endocrinology & Metabolism
- Publisher
- Elsevier BV
- Published
- 2010-10
- Volume
- 24
- Issue
- 5
- Pages
- 785-800
- ISSN
- 1521-690X (ISSN-L)
- PMC
- PMC3011935
- OpenAlex
- W2043741320
- Cited by
- 192
- References
- 94
- Citations by year
- 2026: 5 · 2025: 17 · 2024: 12 · 2023: 11 · 2022: 8 · 2021: 13 · 2020: 12 · 2019: 12 · 2018: 12 · 2017: 16 · 2016: 12 · 2015: 14 · 2014: 8 · 2013: 14 · 2012: 18
- FWCI
- 1.26
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Best Practice & Research Clinical Endocrinology & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- e-Publications@Marquette (Marquette University) (submittedVersion)
- Funders
- National Institute on Aging (P01AG011412)
- National Heart, Lung, and Blood Institute (T32HL007909)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Health Sciences › Medicine › Physiology (medical) › Dietary Effects on Health
- Keywords
- circadian rhythm disruption, metabolic disorders, animal models, nocturnal activity, circadian system, metabolic dysfunction, translational research
- MeSH terms
- Animals, Biological Clocks, Brain, Circadian Rhythm, Disease Models, Animal, Humans, Metabolic Diseases, Models, Biological, Photoperiod, Sleep Disorders, Circadian Rhythm
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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