The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
The Cytokine Response to Physical Activity and Training
Open accessAbstract
AbstractCytokines are soluble glycoproteins that are produced by and mediate communication between and within immune and nonimmune cells, organs and organ systems throughout the body. Pro- and anti-inflammatory mediators constitute the inflammatory cytokines, which are modulated by various stimuli, including physical activity, trauma and infection. Physical activity affects local and systemic cytokine production at different levels, often exhibiting striking similarity to the cytokine response to trauma and infection.The present review examines the cytokine response to short term exercise stress, with an emphasis on the balance between pro- and anti-inflammatory mechanisms and modulation of both innate and specific immune parameters through cytokine regulation. The effects of long term exercise on cytokine responses and the possible impact on various facets of the immune system are also discussed, with reference to both cross-sectional and longitudinal studies of exercise training. Finally, the validity of using exercise as a model for trauma and sepsis is scrutinised in the light of physiological changes, symptomatology and outcome, and limitations of the model are addressed.Further studies, examining the effect of exercise, trauma and infection on novel cytokines and cytokine systems are needed to elucidate the significance of cytokine regulation by physical activity and, more importantly, to clarify the health implications of short and long term physical activity with respect to overall immune function and resistance to infection.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Detection of circulating tumor necrosis factor after endotoxin administration
Michie, H. R., Manogue, K. R., Spriggs, D. R., Revhaug, A., O'Dwyer, S., Dinarello, C. A., Cerami, A., Wolff, S. M., & Wilmore, D. W. (1988) · New England Journal of Medicine · doi:10.1056/nejm198806093182301 · Cited by 1,677 · cited 1×
“IL-1β ↑ P (H, O) 3h after bacterial infection[190,191]”
BackgroundT cell interleukin-17 induces stromal cells to produce proinflammatory and hematopoietic cytokines
Fossiez, F., Djossou, O., Chomarat, P., Flores-Romo, L., Ait-Yahia, S., Maat, C., Pin, J. J., Garrone, P., Garcia, E., Saeland, S., et al. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.183.6.2593 · Cited by 1,526 · cited 1×
“of pro-inflammatory and haemopoietic cytokines, as well as the IFNγ-inducing factor, IL-18, may also be revealing.[208-210] LIF, a pleiotropic cytok-”
BackgroundRegulation of the Hypothalamic-Pituitary-Adrenal Axis by Cytokines: Actions and Mechanisms of Action
TURNBULL, A. V., & RIVIER, C. L. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.1.1 · Cited by 1,297
Pro‐ and anti‐inflammatory cytokine balance in strenuous exercise in humans
Ostrowski, K., Rohde, T., Asp, S., Schjerling, P., & Pedersen, B. K. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.287ad.x · Cited by 1,014
Muscle function after exercise-induced muscle damage and rapid adaptation
CLARKSON, P. M., NOSAKA, K., & BRAUN, B. (1992) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-199205000-00004 · Cited by 970 · cited 6×
“Reduced heavy-light filament overlap resulting in decreased contractile force[160] Macrophage/monocyte activation, mainly for regenerative role[147,161]”
BackgroundInfluentialAdmission criteria for immunogerontological studies in man: The senieur protocol
Ligthart, G. J., Corberand, J. X., Fournier, C., Galanaud, P., Hijmans, W., Kennes, B., Müller-Hermelink, H. K., & Steinmann, G. G. (1984) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(84)90152-0 · Cited by 754 · cited 1×
“[150] determined that, compared with young individuals, the elderly (mean age 74 years) had significantly elevated IL-6, TNFα and IL-1β levels in the supernatants of mitogenstimulated cultures.”
ResultCarbohydrate and the cytokine response to 2.5 h of running
Nehlsen-Cannarella, S. L., Fagoaga, O. R., Nieman, D. C., Henson, D. A., Butterworth, D. E., Schmitt, R. L., Bailey, E. M., Warren, B. J., Utter, A., & Davis, J. M. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.82.5.1662 · Cited by 311
St Pierre, B. A., & Tidball, J. G. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.1.290 · Cited by 251 · cited 1×
“At the molecular level, thiol proteases such as calpain mediate protein degradation of muscle myofibrillar complexes, with depletion of sarcomeric Disruption of striation pattern [158] Mild neutrophil activation but not cause of tissue damage [159] Reduced heavy-light filament overlap resulting in decreased contractil…”
BackgroundInfluence of mode and carbohydrate on the cytokine response to heavy exertion
NIEMAN, D. C., NEHLSEN-CANNARELLA, S. L., FAGOAGA, O. R., HENSON, D. A., UTTER, A., DAVIS, J. M., WILLIAMS, F., & BUTTERWORTH, D. E. (1998) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199805000-00005 · Cited by 233
Cited by
Sawka, M. N., Leon, L. R., Montain, S. J., & Sonna, L. A. (2011) · Comprehensive Physiology · doi:10.1002/cphy.c100082 · Cited by 470
Nicklas, B. J., Ambrosius, W., Messier, S. P., Miller, G. D., Penninx, B. W., Loeser, R. F., Palla, S., Bleecker, E., & Pahor, M. (2004) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.4.544 · Cited by 443
Exercise modulates oxidative stress and inflammation in aging and cardiovascular diseases
Sallam, N., & Laher, I. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/7239639 · Cited by 334
Nicklas, B. J. (2005) · Canadian Medical Association Journal · doi:10.1503/cmaj.1040769 · Cited by 259
Exercise training changes IL-10/TNF-α ratio in the skeletal muscle of post-MI rats
Batista Jr., M. L., Rosa, J. C., Lopes, R. D., Lira, F. S., Martins Jr., E., Yamashita, A. S., Brum, P. C., Lancha Jr., A. H., Lopes, A. C., & Seelaender, M. (2010) · Cytokine · doi:10.1016/j.cyto.2009.10.007 · Cited by 117
Pakiz, B., Flatt, S. W., Bardwell, W. A., Rock, C. L., & Mills, P. J. (2011) · International Journal of Behavioral Medicine · doi:10.1007/s12529-010-9079-8 · Cited by 104
Cytokine levels in euthymic bipolar patients
Guloksuz, S., Aktas Cetin, E., Cetin, T., Deniz, G., Oral, E. T., & Nutt, D. J. (2010) · Journal of Affective Disorders · doi:10.1016/j.jad.2010.04.027 · Cited by 102
Beyond muscles: The untapped potential of creatine
Riesberg, L. A., Weed, S. A., McDonald, T. L., Eckerson, J. M., & Drescher, K. M. (2016) · International Immunopharmacology · doi:10.1016/j.intimp.2015.12.034 · Cited by 95
Chronic exercise decreases cytokine production in healthy rat skeletal muscle
Lira, F. S., Koyama, C. H., Yamashita, A. S., Rosa, J. C., Zanchi, N. E., Batista, M. L., & Seelaender, M. C. (2009) · Cell Biochemistry and Function · doi:10.1002/cbf.1594 · Cited by 82
Brupbacher, G., Gerger, H., Zander-Schellenberg, T., Straus, D., Porschke, H., Gerber, M., von Känel, R., & Schmidt-Trucksäss, A. (2021) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2021.101452 · Cited by 64
Kinugawa, T., Kato, M., Ogino, K., Osaki, S., Tomikura, Y., Igawa, O., Hisatome, I., & Shigemasa, C. (2003) · International Journal of Cardiology · doi:10.1016/s0167-5273(02)00200-0 · Cited by 48
Gundersen, Y., Opstad, P. K., Reistad, T., Thrane, I., & Vaagenes, P. (2006) · European Journal of Applied Physiology · doi:10.1007/s00421-006-0150-8 · Cited by 34
Molecular Dambusters: What Is Behind Hyperpermeability in Bradykinin-Mediated Angioedema?
Debreczeni, M. L., Németh, Z., Kajdácsi, E., Farkas, H., & Cervenak, L. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-021-08851-8 · Cited by 25
Metadata
- Authors
- Moldoveanu, A. I., Shephard, R. J., & Shek, P. N.
- Venue
- Sports Medicine
- Published
- 2001
- Volume
- 31
- Issue
- 2
- Pages
- 115-144
- ISSN
- 0112-1642 (ISSN-L)
- OpenAlex
- W2016723372
- Cited by
- 325
- References
- 9
- FWCI
- 10.71
- Type
- journal article
- Language
- en
- Open access
- bronze
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.