2004
DOI: 10.1016/j.ehj.2003.12.006
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Exercise reduces plasma levels of the chemokines MCP-1 and IL-8 in subjects with the metabolic syndrome

Abstract: The protective effect of exercise might in part be due to suppression of the inflammatory process.

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Cited by 160 publications
(119 citation statements)
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“…We observed reduction of markers of systemic inflammation and fatigue symptoms. The results of our study agreed with several previous studies suggesting 12-weeks aerobic exercise training program promotes the modulation of systemic inflammation and fatigue symptoms of obese patients with type 2 diabetes [27][28][29][30][31][32][33][34][35][36][37][38][39] . Rosety-Rodriguez and colleagues conducted a 12-week arm cranking exercise program for spinal cord injury patients at a moderate work intensity of 50% to 65% of heart rate reserve for of 3 sessions per week .…”
Section: African Health Sciences Vol 15 Issue 4 December 2015supporting
confidence: 93%
“…We observed reduction of markers of systemic inflammation and fatigue symptoms. The results of our study agreed with several previous studies suggesting 12-weeks aerobic exercise training program promotes the modulation of systemic inflammation and fatigue symptoms of obese patients with type 2 diabetes [27][28][29][30][31][32][33][34][35][36][37][38][39] . Rosety-Rodriguez and colleagues conducted a 12-week arm cranking exercise program for spinal cord injury patients at a moderate work intensity of 50% to 65% of heart rate reserve for of 3 sessions per week .…”
Section: African Health Sciences Vol 15 Issue 4 December 2015supporting
confidence: 93%
“…Here, again, polymorphisms in immune genes modulate risk, implying a pathogenetic significance for immune gene products Table 4 Interventions that have an impact on the inflammatory state Inflammatory mediators whose concentrations are reduced by weight loss and/or physical exercise [190][191][192][193][194][195][196][197][198][199][200][201][202][203][204][205][206][207] CRP, TNF-α, soluble TNF-α receptor 2, IL-6, IL-18, MCP-1, PAI-1, t-PA, soluble ICAM-1, soluble VCAM-1, P-selectin Inflammatory mediators whose concentrations are reduced by glucose-lowering drugs [186,188,[208][209][210][211][212][213][214][215][216][217] Sulphonylurea: TNF-α Metformin: CRP Glitazones: CRP, SAA, TNF-α, soluble CD40 ligand, PAI-1 Insulin: CRP, IL-1, IL-6, TNF-α, soluble ICAM-1, MCP-1, PAI-1 SAA Serum amyloid A, t-PA tissue plasminogen activator, VCAM-1 vascular cell adhesion molecule-1 [171][172][173]. Where studied, the upregulation of inflammatory mediators was linked to increased oxidative stress, impaired mitochondrial function and abnormal cholesterol metabolism [174][175][176].…”
Section: Low-grade Inflammation and Healthmentioning
confidence: 99%
“…Given that human adipose tissue is also metabolically active and able to secrete MCP-1 (13), it has recently been reported that reduction in visceral fat is directly correlated to a decrease in MCP-1 levels (14), supporting a role for VAT in the systemic inflammatory condition. At present, to our knowledge, literature about the correlation between MCP-1 and abdominal adiposity is still scarce and poor evidence has been provided about a correlation between MCP-1 secretion and the VAT entity in humans (12).…”
Section: Introductionmentioning
confidence: 99%