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Exercise and inflammation

炎症 医学 内科学 物理疗法 物理医学与康复
作者
Mark A. Febbraio
出处
期刊:Journal of Applied Physiology [American Physiological Society]
卷期号:103 (1): 376-377 被引量:62
标识
DOI:10.1152/japplphysiol.00414.2007
摘要

HIGHLIGHTED TOPICExercise and InflammationExercise and inflammationMark A. FebbraioMark A. FebbraioPublished Online:01 Jul 2007https://doi.org/10.1152/japplphysiol.00414.2007This is the final version - click for previous versionMoreSectionsPDF (40 KB)Download PDF ToolsExport citationAdd to favoritesGet permissionsTrack citations ShareShare onFacebookTwitterLinkedInWeChat the purpose of this review series is to highlight the tremendous advancement in knowledge that has taken place over the last five to ten years regarding the interaction between physical exercise and inflammation. Many years ago, it was recognized that regular, moderate exercise reduced the risk of infection compared with a sedentary lifestyle, whereas prolonged, heavy intensity exercise increased infection risk; the so called "J-shaped model" (16). However, the precise nexus between physical activity, inflammation, and immunity has, until recently, been unknown, as studies in this area, and the conclusions they made, were largely based on descriptive data analysis. Indeed, in a comprehensive review on exercise and immune function, published at the turn of the millennium, Pedersen and Hoffman Goetz (18) recognized this and commented, "The focus of future work in exercise immunology should move beyond descriptive, phenomenological studies to studies of underlying neural, hormonal, cytokine, and biochemical mechanisms for the observed effects." It must be said that researchers in the field have heeded this message, and this can be clearly observed from the present review series.In the first of the series, Gleeson (7) reviews the literature relating to immune function in sport and exercise. One new and exciting development in this field, from work conducted in Dr. Gleeson's laboratory, is the role that Toll-like receptors (TLRs) play in the immune response in humans during exercise. TLR's are an evolutionary, conserved family of pattern recognition receptors known to play an essential role in detecting infection in both Drosophila and mammals (9). In a paper by Lancaster et al. (13), the authors demonstrated that physical activity decreased the expression of TLR1, TLR2, and TLR4 and concluded that TLR function is subject to modulation under physiological conditions in vivo. Intriguingly, physical exercise is known to increase circulating heat shock proteins (23), which are known to activate TLR2 and TLR4 (1), highlighting the complexity of the immune system in response to physical exercise. The theme of exercise and immune function is continued in the review by Cooper (4), who proposes the theory that exercise elicits an immunological danger type of stress that, on occasions, becomes dysregulated and detrimental to well-being. This view is consistent with that of Matzinger (14), who was the first to challenge the "self versus non-self" theory of immune function, a proposed model of immunity based on the idea that the immune system is more concerned with molecules that do damage rather than those that are foreign. In his review, Dr. Cooper provides various instances of the "danger theory" in the context of strenuous exercise. For example, he points out that food-sensitizing immune cells are relatively innocuous in homeostasis. However, in cases of exercise anaphylaxis, these cells are redistributed from depots such as the spleen into the central circulation where they are no longer harmless.The other reviews in this series center on the role of the contracting skeletal muscle in the interaction between exercise and inflammation. It is in this area that a tremendous amount of knowledge has been obtained in recent years, and the muscle can no longer be regarded as the organ whose role is purely to allow for locomotion. In their review, Pedersen and colleagues (17) suggest that, like the adipose tissue that produces adipokines that circulate and affect metabolic processes (20), skeletal muscle produces "myokines" that also affect metabolism. This work was largely based on important findings that skeletal muscle is the site for production of the cytokine interleukin-6 (IL-6; Ref. 88), contracting muscle releases this cytokine into the circulation (21), and during exercise the release of this cytokine is one of the so-called "work factors" that modulates hepatic glucose production during physical exercise (5). On the basis of the papers by Pedersen and her coworkers, the authors argue that the skeletal muscle can now be viewed as an endocrine organ. The authors provide a review of recent papers from both their group and others that show that other interleukins, namely IL-8 and IL-15, are also produced by skeletal muscle.What leads to cytokine production in skeletal muscle with the onset of contraction? In the next review article (11), Kramer and Goodyear (11) present an informative review that suggests that two major signal transduction pathways, namely the mitogen-activated protein kinases (MAPK) and nuclear factor-κB (NF-κB), are upregulated by muscle contraction. In their review the authors suggest that during low-intensity exercise, contraction activates the extracellular signal-regulated kinases (ERK1/2), which enhance fat metabolism, possibly via the recruitment of the putative fatty acid transporter CD36 (22). In contrast, during heavy activity, p38 MAPK is activated and leads to the upregulation of various metabolic genes via activation of key transcription factors myocyte enhancing factor (MEF)-2 and activating transcription factor (ATF)-2. Next, the authors review the literature relating to NF-κB, which is known as the master controller of inflammation and critical to the life and/or death of a cell (10). Drs. Kramer and Goodyear point out that activation of NF-κB can be paradoxical, resulting in health benefits in some circumstances and disease in others. In doing so, this review highlights some important questions that suggest that NF-κB in skeletal muscle may indeed be unique when compared with other tissues or organs or cells. Why, for example does chronic activation of the upstream kinase, I Kappa kinase (IKK), result in profound insulin resistance and production of IL-6 in liver (3), whereas no such effects are seen in skeletal muscle (2)? It may well be because skeletal muscle is dynamic and undergoes rapid homeostatic alterations during contraction, and, as such, evolution has allowed for it to be protected against such disruption to homeostasis.Finally, Frost and Lang (6) review the literature with respect to the role of acute transforming retrovirus thymoma (Akt), also known as protein kinase B (PKB). This is indeed an heroic task as there are three isoforms of this kinase (Akt1–3); multiple inputs into activation, including growth factor receptors, nutrients, and muscle contraction per se; and several downstream targets associated with anabolism and nutrient delivery to the cell. One section of their review that is both thought provoking and important is the role of Akt in the regulation of the important transcriptional coactivator, peroxisome proliforator-activated receptor gamma coactivator (PGC)-1α. In skeletal muscle, PGC-1α inhibits the expression of atrogenes MuRF-1 and MAFbx (19), and it is known that PGC-1α expression is reduced in diseases such as Type 2 diabetes (15). During exercise, PGC-1α expression is increased (24), and, importantly, in a recent study, treatment of mice with resveratrol, a polyphenol found in red wine and known to extend life span in Drosophila and Caenorhabdtis elegans (25), protected mice against diet-induced obesity and insulin resistance (12). Importantly, in this recent study (12), the authors were able to show that the effects of resveratrol were largely mediated by increased activation of PGC-1α. Could it be that much of the beneficial health effects of exercise are due to the upregulation of PGC-1α in muscle by contraction? These questions and many others are raised by this comprehensive series of reviews published in this Highlighted Topic series in the Journal of Applied Physiology.REFERENCES1 Asea A, Rehli M, Kabingu E, Boch JA, Bare O, Auron PE, Stevenson MA, Calderwood SK. Novel signal transduction pathway utilized by extracellular HSP70: role of toll-like receptor (TLR) 2 and TLR4. J Biol Chem 277: 15028–10534, 2002.Crossref | PubMed | ISI | Google Scholar2 Cai D, Frantz JD, Tawa NE Jr, Melendez PA, Oh BC, Lidov HG, Hasselgren PO, Frontera WR, Lee J, Glass DJ, Shoelson SE. IKKbeta/NF-kappaB activation causes severe muscle wasting in mice. Cell 119: 285–298, 2004.Crossref | PubMed | ISI | Google Scholar3 Cai D, Yuan M, Frantz DF, Melendez PA, Hansen L, Lee J, Shoelson SE. Local and systemic insulin resistance resulting from hepatic activation of IKK-beta and NF-kappaB. Nat Med 11: 183–190, 2005.Crossref | PubMed | ISI | Google Scholar4 Cooper DM. Dangerous exercise—lessons learned from dysregulated inflammatory responses to physical activity. J Appl Physiol. In press; doi:10.1152/japplphysiol.00225.2007.Google Scholar5 Febbraio MA, Hiscock N, Sacchetti M, Fischer CP, Pedersen BK. Interleukin-6 is a novel factor mediating glucose homeostasis in skeletal muscle contraction. Diabetes 53: 1643–1648, 2004.Crossref | PubMed | ISI | Google Scholar6 Frost RA, Lang CH. Protein kinase B/Akt: a nexus of growth factor and cytokine signaling in determining muscle mass. J Appl Physiol. In press; doi:10.1152/jappl.00089.2007.Google Scholar7 Gleeson M. Immune function in sport and exercise. J Appl Physiol. In press; doi:101152/japplphysiol.00008.2007.Google Scholar8 Hiscock N, Chan MH, Bisucci T, Darby IA, Febbraio MA. Skeletal myocytes are the source of interleukin-6 mRNA expression and protein release during contraction: evidence of fiber type specificity. FASEB J 18: 992–994, 2004.Crossref | PubMed | ISI | Google Scholar9 Janeway CA, Medzhitov R. Innate immune recognition. Annu Rev Immunol 20: 197–216, 2002.Crossref | PubMed | ISI | Google Scholar10 Karin M, Lin A. NF-kappaB at the crossroads of life and death. Nat Immunol 3: 221–227, 2002.Crossref | PubMed | ISI | Google Scholar11 Kramer HF, Goodyear LJ. Exercise, MAPK, and NF-κB signaling in skeletal muscle. J Appl Physiol. In press; doi:10.1152/japplphysiol.00085-2007.Google Scholar12 Lagouge M, Argmann C, Gerhart-Hines Z, Meziane H, Lerin C, Daussin F, Messadeq N, Milne J, Lambert P, Elliott P, Geny B, Laakso M, Puigserver P, Auwerx J. Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha. Cell 127: 1109–1122, 2006.Crossref | PubMed | ISI | Google Scholar13 Lancaster GI, Khan Q, Drysdale P, Wallace F, Jeukendrup AE, Drayson MT, Gleeson M. The physiological regulation of toll-like receptor expression and function in humans. J Physiol 563: 945–955, 2005.Crossref | PubMed | ISI | Google Scholar14 Matzinger P. The danger model: a renewed sense of self. Science 296: 301–305, 2002.Crossref | PubMed | ISI | Google Scholar15 Mootha VK, Lindgren CM, Eriksson KF, Subramanian A, Sihag S, Lehar J, Puigserver P, Carlsson E, Ridderstrale M, Laurila E, Houstis N, Daly MJ, Patterson N, Mesirov JP, Golub TR, Tamayo P, Spiegelman B, Lander ES, Hirschhorn JN, Altshuler D, Groop LC. PGC-1α responsive genes involved in oxidative phosphorylation are co-ordinately downregulated in human diabetes. Nat Genet 34: 267–273, 2003.Crossref | PubMed | ISI | Google Scholar16 Nieman DC. Exercise, infection, immunity. Int J Sports Med. 15, Suppl 3: S131–S141, 1994.Crossref | ISI | Google Scholar17 Pedersen BK, Akerstrom TC, Nielsen AR, Fischer CP. Role of myokines in exercise and metabolism. J Appl Physiol. In press; doi:10.1152/japplphysiol.00080.2007.Google Scholar18 Pedersen BK, Hoffman-Goetz L. Exercise and the immune system: regulation, integration, and adaptation. Physiol Rev 80: 1055–1081, 2000.Link | ISI | Google Scholar19 Sandri M, Lin J, Handschin C, Yang W, Arany ZP, Lecker SH, Goldberg AL, Spiegelman BM. PGC-1alpha protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription. Proc Natl Acad Sci USA 103: 16260–16265, 2006.Crossref | PubMed | ISI | Google Scholar20 Scherer PE. Adipose tissue: from lipid storage compartment to endocrine organ. Diabetes 55: 1537–1545, 2006.Crossref | PubMed | ISI | Google Scholar21 Steensberg A, van Hall G, Osada T, Sacchetti M, Saltin B, Klarlund Pedersen B. Production of interleukin-6 in contracting human skeletal muscles can account for the exercise-induced increase in plasma interleukin-6. J Physiol 529: 237–242, 2000.Crossref | PubMed | ISI | Google Scholar22 Turcotte LP, Raney MA, Todd MK. ERK1/2 inhibition prevents contraction-induced increase in plasma membrane FAT/CD36 content and FA uptake in rodent muscle. Acta Physiol Scand 184: 131–139, 2004.Google Scholar23 Walsh RC, Koukoulas I, Garnham A, Moseley PL, Hargreaves M, Febbraio MA. Exercise increases serum HSP72 in humans. Cell Stress Chaperon 6: 386–393, 2001.Crossref | PubMed | ISI | Google Scholar24 Watt MJ, Southgate RJ, Holmes AG, Febbraio MA. Suppression of plasma free fatty acids upregulates peroxisome proliferator-activated receptor (PPAR) alpha and delta and PPAR coactivator 1alpha in human skeletal muscle, but not lipid regulatory genes. J Mol Endocrinol 33: 533–544, 2004.Crossref | PubMed | ISI | Google Scholar25 Wood JG, Rogina B, Lavu S, Howitz K, Helfand SL, Tatar M, Sinclair D. Sirtuin activators mimic caloric restriction and delay ageing in metazoans. Nature 430: 686–689, 2004.Crossref | PubMed | ISI | Google ScholarAUTHOR NOTESAddress for reprint requests and other correspondence: M. A. Febbraio, Cellular & Molecular Metabolism Laboratory, Diabetes & Metabolism Division, Baker Heart Research Institute, PO Box 6492 St Kilda Road Central VIC, 8008, Australia (e-mail: [email protected]) Download PDF Previous Back to Top Next FiguresReferencesRelatedInformation Cited ByEx vivo LPS-stimulated cytokine production is associated with hydration status in community-dwelling middle-to-older-aged adults15 February 2023 | European Journal of Nutrition, Vol. 62, No. 4Endothelial Function14 April 2023Effect of high-intensity exercise on endoplasmic reticulum stress and proinflammatory cytokine levelsScience & Sports, Vol. 9Comparisons of the Prevalence, Severity, and Risk Factors of Dysmenorrhea between Japanese Female Athletes and Non-Athletes in Universities21 December 2021 | International Journal of Environmental Research and Public Health, Vol. 19, No. 1Endometriosis: Epidemiology, Classification, Pathogenesis, Treatment and Genetics (Review of Literature)29 September 2021 | 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Blood Biomarkers Related to Brain Injury28 September 2018 | Frontiers in Physiology, Vol. 9White matter pathways as both a target and mediator of health behaviors11 May 2018 | Annals of the New York Academy of Sciences, Vol. 1428, No. 1Physical Inactivity is not the Same as Sedentarism: The Harm of Prolonged Sitting to Human Health5 June 2017 | MOJ Anatomy & Physiology, Vol. 3, No. 5Factors influencing the post-exercise hepcidin-25 response in elite athletes13 April 2017 | European Journal of Applied Physiology, Vol. 117, No. 6Level and correlates of physical activity and sedentary behavior in patients with type 2 diabetes: A cross-sectional analysis of the Italian Diabetes and Exercise Study_214 March 2017 | PLOS ONE, Vol. 12, No. 3Factors associated with increased irisin levels in the type 1 diabetes mellitus17 February 2017 | Endocrine Regulations, Vol. 51, No. 1Efficacy of exercise on pelvic pain and posture associated with endometriosis: within subject designJournal of Physical Therapy Science, Vol. 29, No. 12Post-traumatic Stress Disorder and Cardiovascular Disease27 August 2016 | Current Cardiology Reports, Vol. 18, No. 10Modulation of Hallmarks of Brain Aging by Environmental Enrichment15 December 2016New trends in food science: the use of nutraceuticals as an antiinflammatory therapeutic tool in exerciseHepatoprotective Effect of Quercetin on Endoplasmic Reticulum Stress and Inflammation after Intense Exercise in Mice through Phosphoinositide 3-Kinase and Nuclear Factor-Kappa BOxidative Medicine and Cellular Longevity, Vol. 2016Impact of Physical Activity on Pain Perception in an Animal Model of Endometriosis24 December 2015 | Journal of Endometriosis and Pelvic Pain Disorders, Vol. 7, No. 3Changes in circulating cytokines and markers of muscle damage in elite cyclists during a multi-stage competition26 May 2014 | Clinical Physiology and Functional Imaging, Vol. 35, No. 5Effect of a 12-week walking exercise program on body composition and immune cell count in patients with breast cancer who are undergoing chemotherapy30 September 2015 | Journal of Exercise Nutrition & Biochemistry, Vol. 19, No. 3Inflammatory cytokine expression in the quadriceps of rats with posttraumatic knee stiffness: A preliminary studyCytokine, Vol. 73, No. 2An official European Respiratory Society statement on physical activity in COPD30 October 2014 | European Respiratory Journal, Vol. 44, No. 6Docosahexanoic acid diet supplementation attenuates the peripheral mononuclear cell inflammatory response to exercise following LPS activationCytokine, Vol. 69, No. 2The many roles of PGC-1α in muscle — recent developmentsMetabolism, Vol. 63, No. 4Endometriosis and physical exercises: a systematic reviewReproductive Biology and Endocrinology, Vol. 12, No. 1The Effects of Diet, Exercise, and Sleep on Brain Metabolism and Function28 January 2014Cardiometabolic Risk Factors in Children18 March 2013 | American Journal of Lifestyle Medicine, Vol. 7, No. 5Physiological Responses to Passive Exercise in Adults Receiving Mechanical VentilationAmerican Journal of Critical Care, Vol. 22, No. 4Physical Activity and Inflammation28 August 2012Resistance exercise training influences skeletal muscle immune activation: a microarray analysisPaul M. Gordon*, Dongmei Liu*, Maureen A. Sartor, Heidi B. IglayReger, Emidio E. Pistilli, Laurie Gutmann, Gustavo A. Nader, and Eric P. Hoffman1 February 2012 | Journal of Applied Physiology, Vol. 112, No. 3The effects of exercise on macrophage functionThe Journal of Physical Fitness and Sports Medicine, Vol. 1, No. 1Increased inflammatory cytokine expression in the vastus lateralis of patients with knee osteoarthritis28 April 2011 | Arthritis & Rheumatism, Vol. 63, No. 5Low Physical Activity and Risk of Cardiovascular and All-Cause Mortality in Renal Transplant RecipientsClinical Journal of the American Society of Nephrology, Vol. 6, No. 4Insulin resistance induced by physical inactivity is associated with multiple transcriptional changes in skeletal muscle in young menA. C. Alibegovic, M. P. Sonne, L. Højbjerre, J. Bork-Jensen, S. Jacobsen, E. Nilsson, K. Færch, N. Hiscock, B. Mortensen, M. Friedrichsen, B. Stallknecht, F. Dela, and A. Vaag1 November 2010 | American Journal of Physiology-Endocrinology and Metabolism, Vol. 299, No. 5Peroxisome proliferator-activated receptor-γ coactivator-1α in muscle links metabolism to inflammationClinical and Experimental Pharmacology and Physiology, Vol. 36, No. 12Inflammation, hepatic enzymes and resistance training in individuals with metabolic risk factorsDiabetic Medicine, Vol. 26, No. 3The role of exercise and PGC1α in inflammation and chronic disease1 July 2008 | Nature, Vol. 454, No. 7203 More from this issue > Volume 103Issue 1July 2007Pages 376-377 Copyright & PermissionsCopyright © 2007 the American Physiological Societyhttps://doi.org/10.1152/japplphysiol.00414.2007PubMed17446409History Published online 1 July 2007 Published in print 1 July 2007 Metrics
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