Stress induces endotoxemia and low-grade inflammation by increasing barrier permeability

被引:208
作者
de Punder, Karin [1 ,2 ]
Pruimboom, Leo [2 ]
机构
[1] Charite, Inst Med Psychol, D-10117 Berlin, Germany
[2] Natura Fdn, Numansdorp, Netherlands
来源
FRONTIERS IN IMMUNOLOGY | 2015年 / 6卷
关键词
endotoxemia; endotoxin; inflammation; intestinal permeability; lipopolysaccharide; stress; tight junction; LIPOPOLYSACCHARIDE-BINDING PROTEIN; PITUITARY-ADRENAL AXIS; HIGH-FAT DIET; INCREASED INTESTINAL PERMEABILITY; SYMPATHETIC-NERVOUS-SYSTEM; ACUTE PSYCHOLOGICAL STRESS; CORONARY-ARTERY-DISEASE; FATIGUE-SYNDROME CFS; FUNCTION IN-VITRO; TIGHT JUNCTION;
D O I
10.3389/fimmu.2015.00223
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic non-communicable diseases (NCDs) are the leading causes of work absence, disability, and mortality worldwide. Most of these diseases are associated with low-grade inflammation. Here, we hypothesize that stresses (defined as homeostatic disturbances) can induce low-grade inflammation by increasing the availability of water, sodium, and energy rich substances to meet the increased metabolic demand induced by the stressor. One way of triggering low-grade inflammation is by increasing intestinal barrier permeability through activation of various components of the stress system. Although beneficial to meet the demands necessary during stress, increased intestinal barrier permeability also raises the possibility of the translocation of bacteria and their toxins across the intestinal lumen into the blood circulation. In combination with modern life-style factors, the increase in bacteria/bacterial toxin translocation arising from a more permeable intestinal wall causes a low-grade inflammatory state. We support this hypothesis with numerous studies finding associations with NCDs and markers of endotoxemia, suggesting that this process plays a pivotal and perhaps even a causal role in the development of low-grade inflammation and its related diseases.
引用
收藏
页数:12
相关论文
共 160 条
[1]   Effect of Lactobacilli on Paracellular Permeability in the Gut [J].
Ahrne, Siv ;
Hagslatt, Marie-Louise Johansson .
NUTRIENTS, 2011, 3 (01) :104-117
[2]   Prevention of gut leakiness by a probiotic treatment leads to attenuated HPA response to an acute psychological stress in rats [J].
Ait-Belgnaoui, Afifa ;
Durand, Henri ;
Cartier, Christel ;
Chaumaz, Gilles ;
Eutamene, Helene ;
Ferrier, Laurent ;
Houdeau, Eric ;
Fioramonti, Jean ;
Bueno, Lionel ;
Theodorou, Vassilia .
PSYCHONEUROENDOCRINOLOGY, 2012, 37 (11) :1885-1895
[3]   Changes in endotoxin levels in T2DM subjects on anti-diabetic therapies [J].
Al-Attas, Omar S. ;
Al-Daghri, Nasser M. ;
Al-Rubeaan, Khalid ;
da Silva, Nancy F. ;
Sabico, Shaun L. ;
Kumar, Sudhesh ;
McTernan, Philip G. ;
Harte, Alison L. .
CARDIOVASCULAR DIABETOLOGY, 2009, 8
[4]   Energy intake is associated with endotoxemia in apparently healthy men [J].
Amar, Jacques ;
Burcelin, Remy ;
Ruidavets, Jean Bernard ;
Cani, Patrice D. ;
Fauvel, Josette ;
Alessi, Marie Christine ;
Chamontin, Bernard ;
Ferrieres, Jean .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 87 (05) :1219-1223
[5]   Physiology and Function of the Tight Junction [J].
Anderson, James M. ;
Van Itallie, Christina M. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2009, 1 (02) :a002584
[6]   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
[7]   Glucose uptake via SGLT-1 is stimulated by β2-adrenoceptors in the ruminal epithelium of sheep [J].
Aschenbach, JR ;
Borau, T ;
Gäbel, G .
JOURNAL OF NUTRITION, 2002, 132 (06) :1254-1257
[8]   Exercise-induced endotoxemia: The effect of ascorbic acid supplementation [J].
Ashton, T ;
Young, IS ;
Davison, GW ;
Rowlands, CC ;
McEneny, J ;
Van Blerk, C ;
Jones, E ;
Peters, JR ;
Jackson, SK .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (03) :284-291
[9]   Exposure to a social stressor alters the structure of the intestinal microbiota: Implications for stressor-induced immunomodulation [J].
Bailey, Michael T. ;
Dowd, Scot E. ;
Galley, Jeffrey D. ;
Hufnagle, Amy R. ;
Allen, Rebecca G. ;
Lyte, Mark .
BRAIN BEHAVIOR AND IMMUNITY, 2011, 25 (03) :397-407
[10]  
Bailey MT, 1999, DEV PSYCHOBIOL, V35, P146, DOI 10.1002/(SICI)1098-2302(199909)35:2<146::AID-DEV7>3.3.CO