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DOI: 10.1055/s-2006-923777
© Georg Thieme Verlag KG Stuttgart · New York
Salivary IgA Response to Intermittent and Continuous Exercise
Publication History
Accepted after revision: November 20, 2005
Publication Date:
16 February 2006 (online)
Abstract
Current evidence would support a view that intense exercise increases whereas moderate exercise reduces the susceptibility to illness, predominately upper respiratory tract infections. Concentrations of IgA and cortisol in saliva may be used to reflect changes in immune function. The aim of this study was to determine if the type of exercise (soccer-specific intermittent or continuous exercise at the same average work-rate and duration) affects salivary IgA (s-IgA) and cortisol responses. In a randomized, counterbalanced design, eight healthy males completed two trials one week apart at the same time of day on a motorized treadmill. One session entailed soccer-specific intermittent exercise, the other involved continuous exercise at the same overall work-rate. Diet and activity were standardized for 48 hours prior to and following each trial. Unstimulated saliva samples were collected via passive expectoration during the week prior to commencement of exercise, before, at half-time, immediately post-exercise, and 6 hours, 24 hours, and 48 hours post-exercise. No significant difference was observed in heart rate between the two exercise conditions (Intermittent: 142 ± 14; Continuous: 141 ± 16 beats · min-1). Average rating of perceived exertion was higher (p < 0.05) in intermittent exercise (11.9 ± 0.8) than during continuous exercise (10.8 ± 1.2). The pattern of change in salivary responses, including solute secretion rate, IgA concentration, IgA secretion rate, IgA to osmolality ratio, cortisol, and cortisol secretion rate did not differ between the two trials (p > 0.05). Concentrations of s-IgA for the intermittent and continuous protocols were 131.6 ± 61.2 vs. 146.4 ± 107.6 before, 148.4 ± 82.5 vs. 229.2 ± 159.6 after, and 125 ± 78.7 vs. 131.1 ± 80.7 48 h post-exercise, respectively. Saliva flow rate decreased and osmolality increased significantly across all time points (p < 0.05). In conclusion, soccer-specific intermittent exercise did not suppress the salivary IgA response or alter cortisol secretion compared to continuous exercise performed at the same overall work-rate.
Key words
Saliva - soccer-specific intermittent exercise - cortisol
References
- 1 Akimoto T, Kumai Y, Akama T, Hayashi E, Murakami H, Soma R, Kuno S, Kono I. Effects of 12 months of exercise training on salivary secretory IgA levels in elderly subjects. Br J Sports Med. 2003; 37 76-79
- 2 Akimoto T, Nakahori C, Aizawa K, Kimura F, Fukubayashi T, Kono I. Acupuncture and responses of immunologic and endocrine markers during competition. Med Sci Sports Exerc. 2003; 35 1296-1302
- 3 Alverdy J, Aoys E. The effect of glucocorticoid administration on bacterial translocation. Evidence for an acquired mucosal immunodeficient state. Ann Surg. 1991; 214 719-723
- 4 Asahi Y, Yoshikawa T, Watanabe I, Iwasak T, Hasegawa H, Sato Y, Shimada S, Nanno M, Matsuoka Y, Ohwaki M, Iwakura Y, Suzuki Y, Aizawa C, Sata T, Kurata T, Tamura S. Protection against influenza virus infection in polymeric Ig receptor knockout mice immunized intranasally with adjuvant-combined vaccines. J Immunol. 2002; 168 2930-2938
- 5 Atkinson G, Nevill A M. Selected issues in the design and analysis of sport performance research. J Sports Sci. 2001; 19 811-827
- 6 Bangsbo J. The physiology of soccer with special reference to intense intermittent exercise. Acta Physiol Scand Suppl. 1994; 619 1-155
- 7 Bird S, Davison R. Physiological Testing Guidelines. Leeds; British Association of Sport and Exercise Sciences 1997
- 8 Bishop N C, Blannin A K, Armstrong E, Rickman M, Gleeson M. Carbohydrate and fluid intake affect the saliva flow rate and IgA response to cycling. Med Sci Sports Exerc. 2000; 32 2046-2051
- 9 Bishop N C, Blannin A K, Robson P J, Walsh N P, Gleeson M. The effects of carbohydrate supplementation on immune responses to a soccer-specific exercise protocol. J Sports Sci. 1999; 17 787-796
- 10 Blannin A K, Robson P J, Walsh N P, Clark A M, Glennon L, Gleeson M. The effect of exercising to exhaustion at different intensities on saliva immunoglobulin A, protein and electrolyte secretion. Int J Sports Med. 1998; 19 547-552
- 11 Borg G A. Psychophysical bases of perceived exertion. Med Sci Sports Exerc. 1982; 14 377-381
- 12 Carli G, Bonifazi M, Lodi L, Lupo C, Marteli G, Viti A. Hormonal and metabolic effects following a football match. Int J Sports Med. 1986; 7 36-38
- 13 Chard T. An Introduction to Radioimmunoassay and Related Techniques. Amsterdam; Elsevier 1990
- 14 Chicharro J L, Lucia A, Perez M, Vaquero A F, Urena R. Saliva composition and exercise. Sports Med. 1998; 26 17-27
- 15 Cole A, Eastoe J. Biochemistry and Oral Biology. London; Wright 1988
- 16 Cupps T R, Fauci A S. Corticosteroid-mediated immunoregulation in man. Immunol Rev. 1982; 65 133-155
- 17 Dawes C. Rhythms in salivary flow rate and composition. Int J Chronobiol. 1974; 2 253-279
- 18 Dimitriou L, Sharp N C, Doherty M. Circadian effects on the acute responses of salivary cortisol and IgA in well trained swimmers. Br J Sports Med. 2002; 36 260-264
- 19 Drust B, Reilly T, Cable N T. Physiological responses to laboratory-based soccer-specific intermittent and continuous exercise. J Sports Sci. 2000; 18 885-892
- 20 Durnin J V, Womersley J. Body fat assessed from total body density and its estimation from skinfold thickness: measurements on 481 men and women aged from 16 to 72 years. Br J Nutr. 1974; 32 77-97
- 21 Filaire E, Lac G, Pequignot J M. Biological, hormonal, and psychological parameters in professional soccer players throughout a competitive season. Percept Mot Skills. 2003; 97 1061-1072
- 22 Fischer H P, Eich W, Russell I J. A possible role for saliva as a diagnostic fluid in patients with chronic pain. Semin Arthritis Rheum. 1998; 27 348-359
- 23 Fox P C, van der Ven P F, Sonies B C, Weiffenbach J M, Baum B J. Xerostomia: evaluation of a symptom with increasing significance. J Am Dent Assoc. 1985; 110 519-525
- 24 Francis J L, Gleeson M, Pyne D B, Callister R, Clancy R L. Variation of salivary immunoglobulins in exercising and sedentary population. Med Sci Sports Exerc. 2005; 37 571-578
- 25 Galbo H. Hormonal and Metabolic Adaptation to Exercise. New York; Thieme-Stratton 1983
- 26 Gleeson M, Hall S T, McDonald W A, Flanagan A J, Clancy R L. Salivary IgA subclasses and infection risk in elite swimmers. Immunol Cell Biol. 1999; 77 351-355
- 27 Gleeson M, McDonald W A, Pyne D B, Cripps A W, Francis J L, Fricker P A, Clancy R L. Salivary IgA levels and infection risk in elite swimmers. Med Sci Sports Exerc. 1999; 31 67-73
- 28 Gleeson M, Pyne D B. Special feature for the Olympics: effects of exercise on the immune system: exercise effects on mucosal immunity. Immunol Cell Biol. 2000; 78 536-544
- 29 Gleeson M, Pyne D B, Callister R. The missing links in exercise effects on mucosal immunity. Exerc Immunol Rev. 2004; 10 107-128
- 30 Goodrich M E, McGee D W. Regulation of mucosal B cell immunoglobulin secretion by intestinal epithelial cell-derived cytokines. Cytokine. 1998; 10 948-955
- 31 Herbert T B, Cohen S. Stress and immunity in humans: a meta-analytic review. Psychosom Med. 1993; 55 364-379
- 32 Hooper S L, MacKinnon L T, Gordon R D, Bachmann A W. Hormonal responses of elite swimmers to overtraining. Med Sci Sports Exerc. 1993; 25 741-747
- 33 Hucklebridge F, Clow A, Evans P. The relationship between salivary secretory immunoglobulin A and cortisol: neuroendocrine response to awakening and the diurnal cycle. Int J Psychophysiol. 1998; 31 69-76
- 34 Isaacs D, Webster A D, Valman H B. Immunoglobulin levels and function in pre-school children with recurrent respiratory infections. Clin Exp Immunol. 1984; 58 335-340
- 35 Jacks D E, Sowash J, Anning J, McGloughlin T, Andres F. Effect of exercise at three exercise intensities on salivary cortisol. J Strength Cond Res. 2002; 16 286-289
-
36 Kugler J.
Biobehavioural influences on respiratory immunity. Schedlowski M, Tewes U Translator and Editor. Psychoneuroimmunology: An Interdisciplinary Introduction. New York; Kluwer Academic/Plenum Publishers 1999 - 37 Lamm M E. Current concepts in mucosal immunity. IV. How epithelial transport of IgA antibodies relates to host defense. Am J Physiol. 1998; 274 G614-G617
- 38 Ljungberg G, Ericson T, Ekblom B, Birkhed D. Saliva and marathon running. Scand J Med Sci Sports. 1997; 7 214-219
- 39 Mackinnon L T. Exercise and Immunology. Champaign, IL; Human Kinetics 1992: 1-115
- 40 Mackinnon L T. Immunoglobulin, antibody and exercise. Exercise Immunology Review. 1996; 2 1-34
- 41 Mackinnon L T, Chick T W, van As A, Tomasi T B. The effect of exercise on secretory and natural immunity. Adv Exp Med Biol. 1987; 216 A 869-876
- 42 Mackinnon L T, Hooper S. Mucosal (secretory) immune system responses to exercise of varying intensity and during overtraining. Int J Sports Med. 1994; 15 (Suppl 3) S179-S183
- 43 Malm C, Ekblom O, Ekblom B. Immune system alteration in response to two consecutive soccer games. Acta Physiol Scand. 2004; 180 143-155
- 44 Mandel I D. Salivary diagnosis: more than a lick and a promise. J Am Dent Assoc. 1993; 124 85-87
- 45 McDowell S L, Chaloa K, Housh T J, Tharp G D, Johnson G O. The effect of exercise intensity and duration on salivary immunoglobulin A. Eur J Appl Physiol. 1991; 63 108-111
- 46 Nieman D C. Current perspective on exercise immunology. Curr Sports Med Rep. 2003; 2 239-242
- 47 Nieman D C. Exercise, upper respiratory tract infection, and the immune system. Med Sci Sports Exerc. 1994; 26 128-139
- 48 Nieman D C, Henson D A, Fagoaga O R, Utter A C, Vinci D M, Davis J M, Nehlsen-Cannarella S L. Change in salivary IgA following a competitive marathon race. Int J Sports Med. 2002; 23 69-75
- 49 Novas A M, Rowbottom D G, Jenkins D G. Tennis, incidence of URTI and salivary IgA. Int J Sports Med. 2003; 24 223-229
- 50 Ostergaard P A. IgA levels, bacterial carrier rate, and the development of bronchial asthma in children. Acta Pathol Microbiol Scand [C]. 1977; 85 187-195
- 51 Pedersen B K, Hoffman-Goetz L. Exercise and the immune system: regulation, integration, and adaptation. Physiol Rev. 2000; 80 1055-1081
- 52 Pilardeau P, Richalet J P, Bouissou P, Vaysse J, Larmignat P, Boom A. Saliva flow and composition in humans exposed to acute altitude hypoxia. Eur J Appl Physiol. 1990; 59 450-453
-
53 Purvis A J, Cable N T.
Effects of exercise mode on foot skin temperature. Spinks W, Reilly T, Murphy A Science and Football IV. London; Routledge 2002: 355-360 - 54 Reilly T, Brooks G A. Exercise and the circadian variation in body temperature measures. Int J Sports Med. 1986; 7 358-362
- 55 Shirreffs S M. Markers of hydration status. J Sports Med Phys Fitness. 2000; 40 80-84
- 56 Tharp G D. Basketball exercise and secretory immunoglobulin A. Eur J Appl Physiol. 1991; 63 312-314
- 57 Tharp G D, Barnes M W. Reduction of saliva immunoglobulin levels by swim training. Eur J Appl Physiol. 1990; 60 61-64
- 58 Thomas J R, Salazar W, Landers D M. What is missing in p less than 0.05? Effect size. Res Q Exerc Sport. 1991; 62 344-348
- 59 Tomasi T B, Trudeau F B, Czerwinski D, Erredge S. Immune parameters in athletes before and after strenuous exercise. J Clin Immunol. 1982; 2 173-178
-
60 Van Gool D, Van Gervan D, Boutmans J.
The physiological load imposed on soccer players during real match play. Reilly T, Lees A, Davids K, Murphy JW Translator and Editor. Science and Football. London; E & FN Spon 1988: 51-59 - 61 Walsh N P, Blannin A K, Clark A M, Cook L, Robson P J, Gleeson M. The effects of high-intensity intermittent exercise on saliva IgA, total protein and alpha-amylase. J Sports Sci. 1999; 17 129-134
- 62 Walsh N P, Montague J C, Callow N, Rowlands A V. Saliva flow rate, total protein concentration and osmolality as potential markers of whole body hydration status during progressive acute dehydration in humans. Arch Oral Biol. 2004; 49 149-154
- 63 Wira C R, Sandoe C P, Steele M G. Glucocorticoid regulation of the humoral immune system. I. In vivo effects of dexamethasone on IgA and IgG in serum and at mucosal surfaces. J Immunol. 1990; 144 142-146
Prof. Thomas Reilly
Liverpool John Moores University, Research Institute for Sport and Exercise Sciences, Henry Cotton Campus
15 - 21 Webster Street
Liverpool, L3 2ET
England
Phone: + 441512314324
Fax: + 44 15 12 31 43 53
Email: t.p.reilly@ljmu.ac.uk