Abstract
Background: Circadian variation in bodily functions has been shown to impact health in acute and chronic medical conditions. Little is known about the relationship between circadian rhythm and sepsis in humans. We aimed to investigate circadian variations in the host response in a human endotoxaemia model. Design and Methods: A cross-over study, where 12 healthy young men received E. coli endotoxin (lipopolysaccharide, LPS) 0.3 ng/kg at 12 noon and, on another day, at 12 midnight. Blood samples were analysed for pro- and anti-inflammatory cytokines: tumour-necrosis factor (TNF)-alpha, soluble TNF receptors (sTNF-R)-1 and -2, interleukin (IL)-1beta, IL-1 receptor antagonist (IL-1Ra), IL-6, and IL-10 as well as YKL-40 and the oxidative stress markers malondialdehyde (MDA), ascorbic acid (AA) and dehydroascorbic acid (DHA) before and at 2, 4, 6 and 8 hours after LPS administration. Results: The levels of MDA and IL-10 where significantly higher during the day time (P<0.05) whereas levels of TNF-alpha, sTNF-RI, sTNF-RII, IL-1Ra, IL-6, and YKL-40 were higher (P<0.01 for all comparisons) during the night time. No significant differences were seen in the levels of AA and DHA. Conclusion: A day-night difference in the acute phase response to endotoxaemia exists in healthy volunteers with a more pronounced inflammatory response during the night time. This circadian difference in the response to endotoxaemia may play an important role in the clinical setting and should be investigated further.
Original language | English |
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Article number | e87413 |
Journal | PloS one |
Volume | 9 |
Issue number | 1 |
Number of pages | 7 |
ISSN | 1932-6203 |
DOIs | |
Publication status | Published - 27 Jan 2014 |
Keywords
- Adipokines
- Analysis of Variance
- Circadian Rhythm
- Cross-Over Studies
- Cytokines
- Endotoxemia
- Humans
- Inflammation
- Interleukin 1 Receptor Antagonist Protein
- Interleukin-10
- Interleukin-1beta
- Interleukin-6
- Lectins
- Lipopolysaccharides
- Male
- Malondialdehyde
- Oxidative Stress
- Receptors, Tumor Necrosis Factor
- Time Factors
- Tumor Necrosis Factor-alpha