Cited by 243Circadian rhythm and melatoninAdipose Tissue and MetabolismLipid metabolism and biosynthesis

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Circadian Regulation of Lipid Mobilization in White Adipose Tissues

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Shostak, Anton, Meyer-Kovac, Judit, Oster, Henrik·2013·Diabetes

DOI 10.2337/db12-1449PMC PMC3712056

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Abstract

In mammals, a network of circadian clocks regulates 24-h rhythms of behavior and physiology. Circadian disruption promotes obesity and the development of obesity-associated disorders, but it remains unclear to which extent peripheral tissue clocks contribute to this effect. To reveal the impact of the circadian timing system on lipid metabolism, blood and adipose tissue samples from wild-type, ClockΔ19, and Bmal1(-/-) circadian mutant mice were subjected to biochemical assays and gene expression profiling. We show diurnal variations in lipolysis rates and release of free fatty acids (FFAs) and glycerol into the blood correlating with rhythmic regulation of two genes encoding the lipolysis pacemaker enzymes, adipose triglyceride (TG) lipase and hormone-sensitive lipase, by self-sustained adipocyte clocks. Circadian clock mutant mice show low and nonrhythmic FFA and glycerol blood content together with decreased lipolysis rates and increased sensitivity to fasting. Instead circadian clock disruption promotes the accumulation of TGs in white adipose tissue (WAT), leading to increased adiposity and adipocyte hypertrophy. In summary, circadian modulation of lipolysis rates regulates the availability of lipid-derived energy during the day, suggesting a role for WAT clocks in the regulation of energy homeostasis.

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Authors: Shostak, A., Meyer-Kovac, J., & Oster, H.
Affiliations: Max Planck Institute for Biophysical Chemistry (DE)
Circadian Rhythms Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany
Corresponding author: Oster, Henrik
ORCID: Shostak, Anton
Oster, Henrik
Venue: Diabetes
Publisher: American Diabetes Association
Published: 2013-06-14
Volume: 62
Issue: 7
Pages: 2195-2203
ISSN: 0012-1797 (ISSN-L)
1939-327X
DOI: 10.2337/db12-1449
PMC: PMC3712056
OpenAlex: W2098360522
Cited by: 243
References: 54
Citations by year: 2026: 12 · 2025: 22 · 2024: 17 · 2023: 23 · 2022: 26 · 2021: 14 · 2020: 22 · 2019: 19 · 2018: 16 · 2017: 17 · 2016: 20 · 2015: 16 · 2014: 14 · 2013: 5
FWCI: 9.90
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-nd
creativecommons.org/licenses/by-nc-nd/3.0/ (vor, 2999 d)
Locations: Diabetes (publishedVersion, cc-by-nc-nd)
PubMed Central (publishedVersion, cc-by-nc-nd)
PubMed (publishedVersion)
MPG.PuRe (Max Planck Society) (submittedVersion)
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
Keywords: circadian clock, white adipose tissue, lipolysis, lipid mobilization, free fatty acids, glycerol, adipose triglyceride lipase, hormone-sensitive lipase, Clock mutant mice, Bmal1, adipocyte hypertrophy, adiposity, energy homeostasis, circadian rhythm disruption
MeSH terms: Animals, Sterol Esterase, Circadian Rhythm, Fatty Acids, Nonesterified, Glycerol, Mice, Knockout, Adiposity, Lipid Metabolism, Mice, Adipose Tissue, White, CLOCK Proteins

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Circadian Regulation of Lipid Mobilization in White Adipose Tissues

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