Pronounced Inflammatory Response to Endotoxaemia during Nighttime: A Randomised Cross-Over Trial

被引:31
作者
Alamili, Mahdi [1 ]
Bendtzen, Klaus [2 ]
Lykkesfeldt, Jens [3 ]
Rosenberg, Jacob [1 ]
Gogenur, Ismail [1 ]
机构
[1] Univ Copenhagen, Herlev Hosp, Dept Surg Gastroenterol, DK-2730 Herlev, Denmark
[2] Rigshosp, Copenhagen Univ Hosp, Inst Inflammat Res, Dept Rheumatol, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Dept Vet Dis Biol, Copenhagen, Denmark
关键词
PLACEBO-CONTROLLED TRIAL; OXIDATIVE STRESS; MENSTRUAL-CYCLE; FREE-RADICALS; IN-VIVO; CYTOKINE RESPONSE; CIRCADIAN-RHYTHM; IMMUNE-SYSTEM; SEPTIC SHOCK; MALONDIALDEHYDE;
D O I
10.1371/journal.pone.0087413
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:7
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共 43 条
[1]  
Alamili M, 2013, CHRONOBIOLOL INT, DOI [10.3109/07420528.2013. 808653, DOI 10.3109/07420528.2013.808653)]
[2]  
Alamili M, 2010, DAN MED BULL, V57
[3]   Human Endotoxemia as a model of systemic inflammation [J].
Andreasen, A. S. ;
Krabbe, K. S. ;
Krogh-Madsen, R. ;
Taudorf, S. ;
Pedersen, B. K. ;
Moller, K. .
CURRENT MEDICINAL CHEMISTRY, 2008, 15 (17) :1697-1705
[4]   Circadian rhythms, sleep, and the menstrual cycle [J].
Baker, Fiona C. ;
Driver, Helen S. .
SLEEP MEDICINE, 2007, 8 (06) :613-622
[5]   Mode of action of endotoxin: Role of free radicals and antioxidants [J].
Bhattacharyya, J ;
Biswas, S ;
Datta, AG .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (03) :359-368
[6]   Endotoxin tolerance: new mechanisms, molecules and clinical significance [J].
Biswas, Subhra K. ;
Lopez-Collazo, Eduardo .
TRENDS IN IMMUNOLOGY, 2009, 30 (10) :475-487
[7]   SPIN TRAPPING OF FREE-RADICALS PRODUCED INVIVO IN HEART AND LIVER DURING ENDOTOXEMIA [J].
BRACKETT, DJ ;
LAI, EK ;
LERNER, MR ;
WILSON, MF ;
MCCAY, PB .
FREE RADICAL RESEARCH COMMUNICATIONS, 1989, 7 (3-6) :315-324
[8]   Crosstalk between the circadian clock circuitry and the immune system [J].
Cermakian, Nicolas ;
Lange, Tanja ;
Golombek, Diego ;
Sarkar, Dipak ;
Nakao, Atsuhito ;
Shibata, Shigenobu ;
Mazzoccoli, Gianluigi .
CHRONOBIOLOGY INTERNATIONAL, 2013, 30 (07) :870-888
[9]   TLR4 and CD14 receptors expressed in rat pineal gland trigger NFKB pathway [J].
Cruz-Machado, Sanseray da Silveira ;
Carvalho-Sousa, Claudia Emanuele ;
Tamura, Eduardo Koji ;
Pinato, Luciana ;
Cecon, Erika ;
Magno Fernandes, Pedro Augusto Carlos ;
Werneck de Avellar, Maria Christina ;
Ferreira, Zulma Silva ;
Markus, Regina Pekelmann .
JOURNAL OF PINEAL RESEARCH, 2010, 49 (02) :183-192
[10]   Proinflammatory cytokines [J].
Dinarello, CA .
CHEST, 2000, 118 (02) :503-508