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Immunomodulatory Effects of Eisenia bicyclis on Innate Immune Cells in Acute Exercise-Stress Rat Model

  • NamKoong, Seung (Department of Physical Therapy, Kangwon National University) ;
  • Cheoung, Eui-Su (DanjeongBio Co., Ltd.) ;
  • Joo, Hae-Mi (Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., Ltd.) ;
  • Jang, Seon-A (Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., Ltd.) ;
  • Yang, Yoon-Jung (Department of Natural Medicine Resources, Semyung University) ;
  • Kang, Se-Chan (Department of Natural Medicine Resources, Semyung University) ;
  • Jang, Ki-Hyo (Department of Food and Nutrition) ;
  • Sohn, Eun-Hwa (Department of Herbal Medicine Resource, Kangwon National University)
  • Received : 2011.05.02
  • Accepted : 2011.05.31
  • Published : 2011.06.30

Abstract

In this study we investigated effects of supplementation with ethyl acetate extracts of the brown alga Eisenia bicyclis on innate immune cells to evaluate the possibilities as an immunomoulator in exercise stress. Twenty male SD rats were divided into four groups and the treatments were as follows: A, no Eisenia bicyclis extract (EBE) (200 mg/kg) intake and maintained at rest ; B, no EBE intake and undergoing exercise ; C, EBE intake and undergoing exercise ; D, EBE intake and maintained at rest. After 5 weeks of oral supplementation, rats were undergoing intensive swimming exercises for 2 h and sacrificed to assess the effects on peritoneal macrophages, spleen cells and natural killer (NK) cells. We showed increasing effects on nitric oxide-inducible nitric oxide synthase (NO-iNOS) production by macrophages and no effects of NK tumoricidal activity and suppressive effects on spleen cell proliferation in exercise group. However, EBE supplementation suppressed NO-iNOS production by macrophages and increased NK tumoricidal activity and spleen cell proliferative response to mitogen in exercise group. Overall, these results that EBE supplementation has differential effects on innate immune response and could be useful as sports nutrition.

Keywords

References

  1. Adams, D. O. and T. A. Hamilton. 1984. The cell biology of macrophage activation. Annu. Rev. Immunol. 2:283-318. https://doi.org/10.1146/annurev.iy.02.040184.001435
  2. Bredt, D. S. and S. H. Snyder. 1994. Nitric oxide: a physiologic messenger molecule. Annu. Rev. Biochem. 63:175-195. https://doi.org/10.1146/annurev.bi.63.070194.001135
  3. Burleson, G. R., J. H. Dean and A. E. Munson. 1995. Methods in immunotoxicology. Wiley-Liss, New York: 197-210.
  4. Ding, A. H., C. F. Nathan and D. J. Stuehr. 1988. Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production. J. Immunol. 141:2407-2412.
  5. Hemmi, H. and N. Ishida. 1980. The immune response of splenic lymphocytes after cimicifugoside treatment in vitro and pretreatment in vivo. J. Pharmacobiodyn. 3:643-648. https://doi.org/10.1248/bpb1978.3.643
  6. Hibbs, J. B., Jr., R. R. Taintor and Z. Vavrin. 1987. Macrophage cytotoxicity: role for L-arginine deiminase and imino nitrogen oxidation to nitrite. Science 235:473-476. https://doi.org/10.1126/science.2432665
  7. Hibbs, J. B., Jr., R. R. Taintor, Z. Vavrin and E. M. Rachlin. 1988. Nitric oxide: a cytotoxic activated macrophage effector molecule. Biochem. Biophys. Res. Commun. 157:87-94. https://doi.org/10.1016/S0006-291X(88)80015-9
  8. Hoffman-Goetz, L., K. M. May and Y. Arumugam. 1994. Exercise training and mouse mammary tumour metastasis. Anticancer Res. 14:2627-2631.
  9. Hu, T., D. Liu, Y. Chen, J. Wu and S. Wang. 2010. Antioxidant activity of sulfated polysaccharide fractions extracted from Undaria pinnitafida in vitro. Int. J. Biol. Macromol. 46: 193-198. https://doi.org/10.1016/j.ijbiomac.2009.12.004
  10. Joe, M. J., S. N. Kim, H. Y. Choi, W. S. Shin, G. M. Park, D. W. Kang and Y. K. Kim. 2006. The inhibitory effects of eckol and dieckol from Ecklonia stolonifera on the expression of matrix metalloproteinase-1 in human dermal fibroblasts. Biol. Pharm. Bull. 29:1735-1739. https://doi.org/10.1248/bpb.29.1735
  11. Kang, K., H. J. Hwang, D. H. Hong, Y. Park, S. H. Kim, B. H. Lee and H. C. Shin. 2004. Antioxidant and antiinflammatory activities of ventol, a phlorotannin-rich natural agent derived from Ecklonia cava, and its effect on proteoglycan degradation in cartilage explant culture. Res. Commun. Mol. Pathol. Pharmacol. 115-116:77-95.
  12. Keller, R., R. Keist and K. Frei. 1990. Lymphokines and bacteria, that induce tumoricidal activity, trigger a different secretory response in macrophages. Eur. J. Immunol. 20: 695-698. https://doi.org/10.1002/eji.1830200334
  13. Madden, K. S. and D. L. Felten. 1995. Experimental basis for neural-immune interactions. Physiol. Rev. 75:77-106. https://doi.org/10.1152/physrev.1995.75.1.77
  14. Mosmann, T. 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65:55-63. https://doi.org/10.1016/0022-1759(83)90303-4
  15. Nielsen, H. B. and B. K. Pedersen. 1997. Lymphocyte proliferation in response to exercise. Eur. J. Appl. Physiol. Occup. Physiol. 75:375-379. https://doi.org/10.1007/s004210050175
  16. Nieman, D. C., A. R. Miller, D. A. Henson, B. J. Warren, G. Gusewitch, R. L. Johnson, J. M. Davis, D. E. Butterworth and S. L. Nehlsen-Cannarella. 1993. Effects of high- vs moderate-intensity exercise on natural killer cell activity. Med. Sci. Sports Exerc. 25:1126-1134.
  17. Okada, Y., A. Ishimaru, R. Suzuki and T. Okuyama. 2004. A new phloroglucinol derivative from the brown alga Eisenia bicyclis: potential for the effective treatment of diabetic complications. J. Nat. Prod. 67:103-105. https://doi.org/10.1021/np030323j
  18. Ostrowski, K., C. Hermann, A. Bangash, P. Schjerling, J. N. Nielsen and B. K. Pedersen. 1998a. A trauma-like elevation of plasma cytokines in humans in response to treadmill running. J. Physiol. 513:889-894. https://doi.org/10.1111/j.1469-7793.1998.889ba.x
  19. Ostrowski, K., T. Rohde, S. Asp, P. Schjerling and B. K. Pedersen. 1999. Pro- and anti-inflammatory cytokine balance in strenuous exercise in humans. J. Physiol. 515:287-291. https://doi.org/10.1111/j.1469-7793.1999.287ad.x
  20. Ostrowski, K., T. Rohde, M. Zacho, S. Asp and B. K. Pedersen. 1998b. Evidence that interleukin-6 is produced in human skeletal muscle during prolonged running. J. Physiol. 508: 949-953. https://doi.org/10.1111/j.1469-7793.1998.949bp.x
  21. Palmo, J., S. Asp, J. R. Daugaard, E. A. Richter, M. Klokker and B. K. Pedersen. 1995. Effect of eccentric exercise on natural killer cell activity. J. Appl. Physiol. 78:1442-1446. https://doi.org/10.1152/jappl.1995.78.4.1442
  22. Pedersen, B. K. and L. Hoffman-Goetz. 2000. Exercise and the immune system: regulation, integration, and adaptation. Physiol. Rev. 80:1055-1081. https://doi.org/10.1152/physrev.2000.80.3.1055
  23. Sprenger, H., C. Jacobs, M. Nain, A. M. Gressner, H. Prinz, W. Wesemann and D. Gemsa. 1992. Enhanced release of cytokines, interleukin-2 receptors, and neopterin after long-distance running. Clin. Immunol. Immunopathol. 63:188-195. https://doi.org/10.1016/0090-1229(92)90012-D
  24. Whitaker, D. M. and G. P. Carlson. 1975. Anti-inflammation mechanism of extract from Eisenia bicyclis (Kjellman) Setchell. J. Pharm. Sci. 64:1258-1259. https://doi.org/10.1002/jps.2600640735
  25. Whiteside, T. L. and R. B. Herberman. 1989. The role of natural killer cells in human disease. Clin. Immunol. Immunopathol. 53:1-23. https://doi.org/10.1016/0090-1229(89)90096-2

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