Fibromyalgia: anti-inflammatory and stress responses after acute moderate exercise

Maria Elena Bote, Juan Jose Garcia, Maria Dolores Hinchado, Eduardo Ortega, Maria Elena Bote, Juan Jose Garcia, Maria Dolores Hinchado, Eduardo Ortega

Abstract

Fibromyalgia (FM) is characterized in part by an elevated inflammatory status, and "modified exercise" is currently proposed as being a good therapeutic help for these patients. However, the mechanisms involved in the exercise-induced benefits are still poorly understood. The objective was to evaluate the effect of a single bout of moderate cycling (45 min at 55% VO2 max) on the inflammatory (serum IL-8; chemotaxis and O2 (-) production by neutrophils; and IL-1β, TNF-α, IL-6, IL-10, and IL-18 release by monocytes) and stress (cortisol; NA; and eHsp72) responses in women diagnosed with FM compared with an aged-matched control group of healthy women (HW). IL-8, NA, and eHsp72 were determined by ELISA. Cytokines released by monocytes were determined by Bio-Plex® system (LUMINEX). Cortisol was determined by electrochemoluminiscence, chemotaxis was evaluated in Boyden chambers and O2 (-) production by NBT reduction. In the FM patients, the exercise induced a decrease in the systemic concentration of IL-8, cortisol, NA, and eHsp72; as well as in the neutrophil's chemotaxis and O2 (-) production and in the inflammatory cytokine release by monocytes. This was contrary to the completely expected exercise-induced increase in all those biomarkers in HW. In conclusion, single sessions of moderate cycling can improve the inflammatory status in FM patients, reaching values close to the situation of aged-matched HW at their basal status. The neuroendocrine mechanism seems to be an exercise-induced decrease in the stress response of these patients.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Effect of an acute session…
Figure 1. Effect of an acute session of moderate exercise (+E) on the serum concentration of IL-8 in healthy women (HW; n = 8) and in FM patients (FM; n = 8).
The results are presented as the mean value ± SEM of a set of independent experiments performed in duplicate (one experiment per volunteer). ***p++p<0.01 with respect to each respective pre-exercise values.
Figure 2. Effect of an acute session…
Figure 2. Effect of an acute session of moderate exercise (+E) on the plasma concentration of cortisol in healthy women (HW; n = 8) and in FM patients (FM; n = 8).
The results are presented as the mean value ± SEM of a set of independent experiments performed in duplicate (one experiment per volunteer). *p+p<0.05 with respect to each respective pre-exercise values.
Figure 3. Effect of an acute session…
Figure 3. Effect of an acute session of moderate exercise (+E) on the plasma concentration of NA in healthy women (HW; n = 8) and in FM patients (FM; n = 8).
The results are presented as the mean value ± SEM of a set of independent experiments performed in duplicate (one experiment per volunteer). *pxp<0.05 with respect to HW (ANOVA);+p<0.05 with respect to each respective pre-exercise values.
Figure 4. Effect of an acute session…
Figure 4. Effect of an acute session of moderate exercise (+E) on the plasma concentration of eHsp72 in healthy women (HW; n = 8) and in FM patients (FM; n = 8).
The results are presented as the mean value ± SEM of a set of independent experiments performed in duplicate (one experiment per volunteer). *p+p<0.05 with respect to each respective pre-exercise values.
Figure 5. Effect of an acute session…
Figure 5. Effect of an acute session of moderate exercise (+E) on the release of cytokines by monocytes.
IL-1β (A), TNF-α (B), IL-6 (C), IL-10 (D) and IL-18 (D) released by monocytes activated by LPS from healthy women (HW; n = 8) and FM patients (FM; n = 8). The results are presented as the mean value ± SEM of a set of independent experiments performed in duplicate (one experiment per volunteer). *p+p<0.05,++p<0.01 with respect to each respective pre-exercise values.
Figure 6. Effect of an acute session…
Figure 6. Effect of an acute session of moderate exercise (+E) on chemotaxis (A) and O2 − production (B) by neutrophils from healthy women (HW; n = 8) and FM patients (FM; n = 8).
The results are presented as the mean value ± SEM of a set of independent experiments performed in duplicate (one experiment per volunteer). ***p+p<0.05,+++p<0.001 with respect to each respective pre-exercise values.

References

    1. Wolfe F, Smythe HA, Yunus MB, Bennett RM, Bombardier C, et al. (1990) The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee. Arthritis Rheum 33: 160–172.
    1. Mannerkorpi K, Iversen MD (2003) Physical exercise in fibromyalgia and related syndromes. Best Pract Res Clin Rheumatol 21: 513–534.
    1. Van West D, Maes M (2001) Neuroendocrine and immune aspects of fibromyalgia. Biodrugs 15: 521–531.
    1. Ploeger HE, Takken T, de Greef MH, Timmons BW (2009) The effects of acute and chronic exercise on inlammatory markers in children and adults with a chronic inflammatory disease: a systematic review. Exerc Immunol Rev 15: 6–41.
    1. Petersen AMW, Pedersen BK (2005) The anti-inflammatory effect of exercise. J Appl Physiol 98: 1154–1162.
    1. Woods JA, Vieira VJ, Keylock KT (2006) Exercise, inflammation, and innate immunity. Neurol Clin 24: 585–599.
    1. Ortega E, García JJ, Bote ME, Martín Cordero L, Escalante Y, et al. (2009) Exercise in fibromyalgia and related inflammatory disorders: Known effects and unknown chances. Exerc Immunol Rev 15: 42–65.
    1. Ortega E, Bote ME, Giraldo E, García JJ (2012) Aquatic exercise improves the Monocyte pro- and anti-inflammatory cytokine production balance in fibromialgia patients. Scand J Med Sci Sports 22: 104–112.
    1. Bote ME, García JJ; Hinchado MD, Ortega E (2012) Inflammatory/Stress feedback dysregulation in women wih fibromyalgia. Neuroimmunomodulation 19: 343–351.
    1. Ortega E, Collazos ME, Maynar M, Barriga C, De la Fuente M (1993) Stimulation of the phagocytic function of neutrophils in sedentary men after acute moderate exercise. Eur J Appl Physiol Occup Physiol 60–64.
    1. Northoff H, Weinstock C, Berg A (1994) The cytokine response to strenuous exercise. Int J Sports Med 15: S167–S171.
    1. Suzuki K, Nakaji S, Yamada M, Totsuka M, Sato K, et al. (2002) Systemic inflammatory response to exhaustive exercise. Cytokine kinetics. Exerc Immunol Rev 8: 6–48.
    1. Meksawan K, Venkatraman JT, Awad AB, Pendergast DR (2004) Effect of dietary fat intake and exercise on inflammatory meidators of the immune system in sedentary men and women. J Am Coll Nutr 23: 331–340.
    1. Peake J, Nosaka K, Suzuki K (2005) Characterization of inflammatory responses to eccentric exercise in humans. Exerc Immunol Rev 11: 64–85.
    1. Giraldo E, García JJ, Hinchado MD, Ortega E (2009) Exercise intensity-dependent changes in the inflammatory response in sedentary women: role of neuroendocrine parameters in the neutrophil phagocytic process and the pro−/anti- inflammatory cytokine balance. Neuroimmunomodulation 16: 237–244.
    1. Ortega E (2003) Neuroendocrine mediators in the modulation of phagocytosis by exercise: physiological implications. Exerc Immunol Rev 9: 70–94.
    1. Ortega E, Giraldo E, Hinchado MD, Martín-Cordero L, De la Fuente M (2007) Neuroimmunomodulation during exercise: role of catecholamines as “stress mediator” and/or “danger signal” for the innate immune response. Neuroimmunomodulation 14: 206–212.
    1. Fleshner M, Campisi J, Johnson JD (2003) Can exercise stress facilitate innate immunity? A functional role for stress-induced extracellular Hsp72. Exerc Immunol Rev 9: 6–24.
    1. Ortega E, Hinchado MD, Martín-Cordero L, Asea A (2009b) The effect of stress inducible extracellular Hsp72 on human neutrophil chemotaxis: a role during acute intense exercise. Stress 12: 240–249.
    1. Ortega E, Giraldo E, Hinchado MD, Martínez M, Ibáñez S, et al. (2006) Role of Hsp72 and norepinephrine in the moderate exercise-induced stimulation of neutrophils’ microbicide capacity. Eur J Appl Physiol 98: 250–255.
    1. Ortega E, Giraldo E, Hinchado MD, Martín-Cordero L, García JJ (2010) 72 kDa extracellular heat shock protein (eHsp72), norepinephrine (NE), and the innate immune response following moderate exercise. In: Asea A, Pedersen BK, ed. Heat Shock Proteins and Whole Body Physiology. Springer, USA 329–350.
    1. Giraldo E, Hinchado MD, García JJ, Ortega E (2008) Influence of gender and oral contraceptives intake on innate and inflammatory response. Role of neuroendocrine factors. Mol Cell Biochem 313: 147–153.
    1. Müller W, Schneider EM, Stratz T (2007) The classification of fibromyalgia syndrome. Rheumatol Int 27: 1005–1010.
    1. Astrand PO, Ryhming I (1954) A nomogram for calculation of aerobic capacity (physical fitness) from pulse rate during sub-maximal work. J Appl Physiol 7: 218–221.
    1. Ortega E, Forner MA, Barriga C (1997) Exercise-induced stimulation of murine macrophage chemotaxis: role of corticosterone and prolactin as mediators. J Physiol 498: 729–734.
    1. Boyden S (1962) The chemotactic effect of mixtures of antibody and antigen on polymorphonuclear leucocytes. J Exp Med 115: 453–466.
    1. Pedersen BK, Saltin B (2006) Evidence for prescribing exercise as therapy in chronic disease. Scand J Med Sci Sports 16: 3–63.
    1. Iizasa H, Matsushima K (2001) Cytokine reference. Oppenheim J.J y Feldman Med, ed. Academic Press. London 1061–1067.
    1. Wallace DJ, Linker-Israeli M, Hallegua D, Silverman S, Silver D, et al. (2001) Cytokines play an aetiopathogenetic role in fibromyalgia: a hypothesis and pilot study. Rheumatol 40: 743–749.
    1. Bazzichi L, Rossi A, Massimetti G, Giannaccini G, Giuliano T, et al. (2007) Cytokine patterns in fibromyalgia and their correlation with clinical manifestations. Clin Exp Rheumatol 25: 225–230.
    1. Giraldo E, Mülthoff G, Ortega E (2010) Noradrenaline increases the expression and release of Hsp72 by human neutrophils. Brain Behav Immun 24: 672–677.
    1. Asea A, Kraeft SK, Kurt-Jones EA, Kurt-Jones EA, Stevenson MA, et al. (2000) Calderwood SK. HSP70 stimulates cytokine production through acd14-dependant pathway, demonstrating its dual role as a chaperone and cytokine. Nat Med 6: 435–442.
    1. Dinarello CA, Novick D, Puren AJ, Fantuzzi G, Shapiro L, et al. (1998) Overview of interleukin-18: more than an interferon-gamma inducing factor. J Leukoc Biol 63: 658–664.
    1. Kohno K, Kurimoto M (1998) Interleukin 18, a cytokine which resembles IL-1 structurally and IL-12 functionally but exerts its effect independently of both. Clin Immunol Immunopathol 86: 11–15.
    1. Ortega Rincón E (1994) Physiology and biochemistry: influence of exercise on phagocytosis. Int J Sports Med 15: 173–178.

Source: PubMed

Подписаться