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The Chemical Characteristics and Immune-Modulating Activity of Polysaccharides Isolated from Cold-Brew Coffee

  • Shin, Kwang-Soon (Department of Food Science and Biotechnology, Kyonggi University)
  • Received : 2017.03.17
  • Accepted : 2017.04.09
  • Published : 2017.06.30

Abstract

To elucidate new biological ingredients in cold-brew coffee extracted with cold water, crude polysaccharide (CCP-0) was isolated by ethanol precipitation, and its immune-stimulating activities were assayed. CCP-0 mainly comprised galactose (53.6%), mannose (15.7%), arabinose (11.9%), and uronic acid (12.4%), suggesting that it might exist as a mixture of galactomannan and arabinogalactan. CCP-0 significantly increased cell proliferation on both murine peritoneal macrophages and splenocytes in a dose dependent manner. CCP-0 also significantly augmented nitric oxide and reactive oxygen species production by murine peritoneal macrophages. In addition, macrophages stimulated by CCP-0 enhanced production of various cytokines such as tumor necrosis factor-${\alpha}$, interleukin (IL)-6, and IL-12. In an in vitro assay for intestinal immune-modulating activity, CCP-0 showed higher bone-marrow cell-proliferation activity through Peyer's patch cells at $100{\mu}g/mL$ than the negative control. These results suggest that CCP-0 may potentially enhance macrophage functions and the intestinal immune system.

Keywords

References

  1. Higdon JV, Frei B. 2006. Coffee and health: a review of recent human research. Crit Rev Food Sci Nutr 46: 101-123. https://doi.org/10.1080/10408390500400009
  2. Kim AR, Kim JS. 2014. Flavor contributing nonvolatile chemical and sensory characterization of cold water extractionbased coffee by different extraction methods (dripping vs steeping) and time. Journal of The Korea Society for Coffee Industry 3: 1-9.
  3. Oh YA, Kim GJ, Yoo SM. 2014. A study on anti-bacterial activity of cold-brewed coffee extracts. Journal of The Korea Society for Coffee Industry 3: 26-33.
  4. Panchal SK, Poudyal H, Waanders J, Brown L. 2012. Coffee extract attenuates changes in cardiovascular and hepatic structure and function without decreasing obesity in highcarbohydrate, high-fat diet-fed male rats. J Nutr 142: 690-697. https://doi.org/10.3945/jn.111.153577
  5. Yukawa GS, Mune M, Otani H, Tone Y, Liang XM, Iwahashi H, Sakamoto W. 2004. Effects of coffee consumption on oxidative susceptibility of low-density lipoproteins and serum lipid levels in humans. Biochemistry 69: 70-74.
  6. Jia H, Aw W, Egashira K, Takahashi S, Aoyama S, Saito K, Kishimoto Y, Kato H. 2014. Coffee intake mitigated inflammation and obesity-induced insulin resistance in skeletal muscle of high-fat diet-induced obese mice. Genes Nutr 9: 389. https://doi.org/10.1007/s12263-014-0389-3
  7. Cano-Marquina A, Tarín JJ, Cano A. 2013. The impact of coffee on health. Maturitas 75: 7-21. https://doi.org/10.1016/j.maturitas.2013.02.002
  8. Arendash GW, Cao C. 2010. Caffeine and coffee as therapeutics against Alzheimer’s disease. J Alzheimers Dis 20: S117-S126. https://doi.org/10.3233/JAD-2010-091249
  9. Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F. 1956. Colorimetric method for determination of sugars and related substances. Anal Chem 28: 350-356. https://doi.org/10.1021/ac60111a017
  10. Blumenkrantz N, Asboe-Hansen G. 1973. New method for quantitative determination of uronic acids. Anal Biochem 54: 484-489. https://doi.org/10.1016/0003-2697(73)90377-1
  11. Bradford MM. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248-254. https://doi.org/10.1016/0003-2697(76)90527-3
  12. Karkhanis YD, Zeltner JY, Jackson JJ, Carlo DJ. 1978. A new and improved microassay to determine 2-keto-3-deoxyoctonate in lipopolysaccharide of Gram-negative bacteria. Anal Biochem 85: 595-601. https://doi.org/10.1016/0003-2697(78)90260-9
  13. Jones TM, Albersheim P. 1972. A gas chromatographic method for the determination of aldose and uronic acid constitulents of plant cell wall polysaccharides. Plant Physiol 49: 926-936. https://doi.org/10.1104/pp.49.6.926
  14. Suzuki I, Tanaka H, Kinoshita A, Oikawa S, Osawa M, Yadomae T. 1990. Effect of orally administered $\beta$-glucan on macrophage function in mice. Int J Immunopharmacol 12: 675-684. https://doi.org/10.1016/0192-0561(90)90105-V
  15. Nunes FM, Coimbra MA. 2002. Chemical characterization of galactomannans and arabinogalactans from two arabica coffee infusions as affected by the degree of roast. J Agric Food Chem 50: 1429-1434. https://doi.org/10.1021/jf0109625
  16. Gordon S. 1998. The role of the macrophage in immune regulation. Res Immunol 149: 685-688. https://doi.org/10.1016/S0923-2494(99)80039-X
  17. Keller R, Keist R, Wechsler A, Leist TP, van der Meide PH. 1990. Mechanisms of macrophage-mediated tumor cell killing: a comparative analysis of the roles of reactive nitrogen intermediates and tumor necrosis factor. Int J Cancer 46: 682-686. https://doi.org/10.1002/ijc.2910460422
  18. Hamilton TA, Adams DO. 1987. Molecular mechanisms of signal transduction in macrophages. Immunol Today 8: 151-158. https://doi.org/10.1016/0167-5699(87)90145-9
  19. Gately MK, Carvajal DM, Connaughton SE, Gillessen S, Warrier RR, Kolinsky KD, Wilkinson VL, Dwyer CM, Higgins GF Jr, Podlaski FJ, Faherty DA, Familletti PC, Stern AS, Presky DH. 1996. Interleukin-12 antagonist activity of mouse interleukin-12 p40 homodimer in vitro and in vivo. Ann NY Acad Sci 795: 1-12. https://doi.org/10.1111/j.1749-6632.1996.tb52650.x
  20. Lasek W, Giermasz A, Kuc K, Wankowicz A, Feleszko W, Golab J, Zagozdzon R, Stoklosa T, Jakobisiak M. 1996. Potentiation of the anti-tumor effect of actinomycin D by tumor necrosis factor $\alpha$ in mice: correlation between in vitro and in vivo results. Int J Cancer 66: 374-379. https://doi.org/10.1002/(SICI)1097-0215(19960503)66:3<374::AID-IJC18>3.0.CO;2-B
  21. Rodriguez-Serrano M, Barany I, Prem D, Coronado MJ, Risueno MC, Testillano PS. 2012. NO, ROS, and cell death associated with caspase-like activity increase in stress-induced microspore embryogenesis of barley. J Exp Bot 63: 2007-2024. https://doi.org/10.1093/jxb/err400
  22. Coleman JW. 2001. Nitric oxide in immunity and inflammation. Int Immunopharmacol 1: 1397-1406. https://doi.org/10.1016/S1567-5769(01)00086-8
  23. Guinazu N, Carrera-Silva EA, Becerra MC, Pellegrini A, Albesa I, Gea S. 2010. Induction of NADPH oxidase activity and reactive oxygen species production by a single Trypanosoma cruzi antigen. Int J Parasitol 40: 1531-1538. https://doi.org/10.1016/j.ijpara.2010.05.012
  24. Gelderman KA, Hultqvist M, Olsson LM, Bauer K, Pizzolla A, Olofsson P, Holmdahl R. 2007. Rheumatoid arthritis: the role of reactive oxygen species in disease development and therapeutic strategies. Antioxid Redox Signal 9: 1541-1568. https://doi.org/10.1089/ars.2007.1569
  25. Ryu DS, Oh SM, Kim KH, Kim SH, Choi HJ, Lee DS. 2010. Immunomodulating activity of Laminaria japonica polysaccharides. Korean J Food Sci Technol 42: 350-354.
  26. Lee SD, Kim DW, Lee I, Lee JH, Hyun SK, Kang KH, Hwang HJ, Kim CM, Kim BW, Chung KT. 2016. Ulmus macrocarpa Hance water extract improved splenocytes survival and NK cell cytotoxicity. J Life Sci 26: 109-116. https://doi.org/10.5352/JLS.2016.26.1.109
  27. Hong T, Matsumoto T, Kiyohara H, Yamada H. 1998. Enhanced production of hematopoietic growth factors through T cell activation in Peyer's patches by oral administration of Kampo (Japanese herbal) medicine, "Juzen-Taiho-To". Phytomedicine 5: 353-360. https://doi.org/10.1016/S0944-7113(98)80017-2
  28. Mestecky J, Elson CO. 2008. Peyer’s patches as the inductive site for IgA responses. J Immunol 180: 1293-1294. https://doi.org/10.4049/jimmunol.180.3.1293
  29. David CW, Norrman J, Hammon HM, Davis WC, Blum JW. 2003. Cell proliferation, apoptosis, and B- and T-lymphocytes in Peyer's patches of the ileum, in thymus and in lymph nodes of preterm calves, and in full-term calves at birth and on day 5 of life. J Dairy Sci 86: 3321-3329. https://doi.org/10.3168/jds.S0022-0302(03)73934-4
  30. Onishi S, Yokoyama T, Chin K, Yuji M, Inamoto T, Qi WM, Warita K, Hoshi N, Kitagawa H. 2007. Ultrastructural study on the differentiation and the fate of M cells in follicle-associated epithelium of rat Peyer’s patch. J Vet Med Sci 69: 501-508. https://doi.org/10.1292/jvms.69.501
  31. Yoon JA, Yu KW, Shin SH, Cho HY. 2010. Activation of intestinal immune system by an orally administered methanol extract from pine needles. J Korean Soc Food Sci Nutr 39: 356-362. https://doi.org/10.3746/jkfn.2010.39.3.356
  32. Parmiani G, Castelli C, Pilla L, Santinami M, Colombo MP, Rivoltini L. 2007. Opposite immune functions of GM-CSF administered as vaccine adjuvant in cancer patients. Ann Oncol 18: 226-232.

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