Browse > Article
http://dx.doi.org/10.3746/jkfn.2013.42.12.1930

Effects of Fermented Soybean Paste Chungkukjang on the Immunoreactivity in Ovariectomized Mice  

Park, Hyunjin (Div. of Food and Nutrition, College of Human Ecology, Sookmyung Women's University)
Yoon, Leena (Div. of Food and Nutritional Science & Life Systems, Sookmyung Women's University)
Kim, Hyun-Sook (Div. of Food and Nutrition, College of Human Ecology, Sookmyung Women's University)
Publication Information
Journal of the Korean Society of Food Science and Nutrition / v.42, no.12, 2013 , pp. 1930-1939 More about this Journal
Abstract
It has been reported that Chungkukjang, one of Korean traditional fermented soybean products, may improve hypertension, diabetes, and hyperlipidemia. In this study, we sought to investigate the immunoenhancing effects of Chungkukjang in ovariectomized mice. For the first period, female SLC ddy mice were either sham-operated (Sham; n=27) or ovariectomized (OVX; n=27). As a basal diet, ovariectomized mice were fed low-calcium diet for faster induction of osteoporosis for six weeks, and those in the Sham group were fed AIN-76 diet. For the second period, half of the OVX group (n=9) and the Sham group (n=9) were fed a Chungkukjang-based diet (CKJ); whereas the other half (OVX; n=9/ Sham; n=9) were fed a casein-based diet (CSI) for 8 weeks. After a second period, we collected the blood via heart puncture and measured the splenocytes proliferation, T lymphocyte subsets by flowcytometry, and levels of serum cytokines (IL-2, IL-4, IL-6, IL-10, IFN-${\gamma}$ and TNF-${\alpha}$) by ELISA assay. The OVX+CKJ group showed higher splenocytes proliferation, higher ratio of CD4/CD8, and lower levels of IL-6 and TNF-${\alpha}$ cytokines compared to the OVX+CSI group. The Sham+CKJ group showed cytokine productions, such as higher levels of IL-10 and IFN-${\gamma}$, and lower levels of IL-6 and TNF-${\alpha}$ compared to the Sham+CSI group. The result of this study suggests that Chungkukjang may lower the proinflammatory cytokine levels in both the OVX and Sham groups. In addition, Chungkukjang could make a balance of T cell subset proliferations and enhance the splenocyte proliferations in the OVX group.
Keywords
Chungkukjang; ovariectomized mice; splenocytes proliferation; T lymphocyte subsets; cytokine production;
Citations & Related Records
Times Cited By KSCI : 5  (Citation Analysis)
연도 인용수 순위
1 Manolagas SC. 2000. Birth and death of bone cells: basic regulatory mechanisms and implications for the pathogenesis and treatment of osteoporosis. Endocr Rev 21: 115-137.
2 McCormick RK. 2007. Osteoporosis: integrating biomarkers and other diagnostic correlates into the management of bone fragility. Altern Med Rev 12: 113-145.
3 Zou W, Amcheslavsky A, Takeshita S, Drissi H, Bar-Shavit Z. 2005. TNF-${\alpha}$ expression is transcriptionally regulated by RANK ligand. J Cell Physiol 202: 371-378.   DOI   ScienceOn
4 Kudo O, Fujikawa Y, Itonaga I, Sabokbar A, Torisu T, Athanasou NA. 2002. Proinflammatory cytokine (TNF${\alpha}$/ IL-1${\alpha}$) induction of human osteoclast formation. J Pathol 198: 220-227.   DOI
5 Komine M, Kukita A, Kukita T, Ogata Y, Hotokebuchi T, Kohashi O. 2001. Tumor necrosis factor-${\alpha}$ cooperates with receptor activator of nuclear factor κB ligand in generation of osteoclasts in stromal cell-depleted rat bone marrow cell culture. Bone 28: 474-483.   DOI   ScienceOn
6 Pacifici R. 1996. Estrogen, cytokines, and pathogenesis of postmenopausal osteoporosis. J Bone Miner Res 11: 1043-1051.
7 Manolagas SC, Jilka RL. 1995. Bone marrow, cytokines, and bone remodeling. Emerging insights into the pathophysiology of osteoporosis. N Engl J Med 332: 305-311.   DOI
8 Brubaker JO, Thompson CM, Morrison LA, Knipe DM, Siber GR, Finberg RW. 1996. Th1-associated immune responses to beta-galactosidase expressed by a replication-defective herpes simplex virus. J Immunol 157: 1598-1604.
9 Snapper CM, Paul WE. 1987. B cell stimulatory factor-1 (interleukin 4) prepares resting murine B cells to secrete IgG1 upon subsequent stimulation with bacterial lipopolysaccharide. J Immunol 139: 10-17.
10 Sugiyama E, Taki H, Kuroda A, Mino T, Yamashita N, Kobayashi M. 1996. Interleukin-4 inhibits prostaglandin E2 production by freshly prepared adherent rheumatoid synovial cells via inhibition of biosynthesis and gene expression of cyclo-oxygenase II but not of cyclo-oxygenase I. Ann Rheum Dis 55: 375-382.   DOI   ScienceOn
11 Suzuki H, Sugiyama E, Tunru IS, Yamashita N, Matsuno H, Hamazaki T, Kobayashi M. 1993. Suppressive effect of interleukin-4 (IL-4) on IL-6 production by adherent rheumatoid synovial cells. Clin Immunol Immunopathol 66: 67-72.   DOI   ScienceOn
12 Hart PH, Cooper RL, Finlay-Jones JJ. 1991. IL-4 suppresses IL-1 beta, TNF-alpha and PGE2 production by human peritoneal macrophages. Immunology 72: 344-349.
13 te Velde AA, Huijbens RJ, Heije K, de Vries JE, Figdor CG. 1990. Interleukin-4 (IL-4) inhibits secretion of IL-1 beta, tumor necrosis factor alpha, and IL-6 by human monocytes. Blood 76: 1392-1397.
14 Miossec P, Chomarat P, Dechanet J, Moreau JF, Roux JP, Delmas P, Banchereau J. 1994. Interleukin-4 inhibits bone resorption through an effect on osteoclasts and proinflammatory cytokines in an ex vivo model of bone resorption in rheumatoid arthritis. Arthritis Rheum 37: 1715-1722.   DOI   ScienceOn
15 Riancho JA, Zarrabeitia MT, Gonzalez-Macias J. 1993. Interleukin-4 modulates osteoclast differentiation and inhibits the formation of resorption pits in mouse osteoclast cultures. Biochem Biophys Res Commun 196: 678-685.   DOI   ScienceOn
16 Joosten LA, Lubberts E, Helsen MM, Saxne T, Coenen-de Roo CJ, Heinegård D, van den Berg WB. 1999. Protection against cartilage and bone destruction by systemic interleukin-4 treatment in established murine type II collagen-induced arthritis. Arthritis Res 1: 81-91.   DOI   ScienceOn
17 Adlercreutz H, Mazur W. 1997. Phyto-oestrogens and Western diseases. Ann Med 29: 95-120.   DOI   ScienceOn
18 Lewis DB, Liggitt HD, Effmann EL, Motley ST, Teitelbaum SL, Jepsen KJ, Goldstein SA, Bonadio J, Carpenter J, Perlmutter RM. 1993. Osteoporosis induced in mice by overproduction of interleukin 4. Proc Natl Acad Sci U S A 90: 11618-11622.   DOI
19 Takayanagi H, Ogasawara K, Hida S, Chiba T, Murata S, Sato K, Takaoka A, Yokochi T, Oda H, Tanaka K, Nakamura K, Taniguchi T. 2000. T-cell-mediated regulation of osteoclastogenesis by signalling cross-talk between RANKL and IFN-${\gamma}$. Nature 408: 600-605.   DOI   ScienceOn
20 Lee BK, Jang YS, Yi SY, Chung KS, Choi SY. 1997. Immunomodulators extracted from Korean-style fermented soybean paste and their function. 1. Isolation of B cell mitogen from Korean-style fermented soybean paste. Korean J Immunol 19: 559-570.
21 Joo EY, Park CS. 2011. Antioxidant and fibrinolytic activities of extracts from soybean and Chungkukjang (fermented soybean paste). Korean J Food Preserv 18: 930-937.   과학기술학회마을   DOI   ScienceOn
22 Ko HS, Cho DH, Hwang SY, Kim YM. 1999. The effect of quality improvement by Chungkuk-jang's processing methods. Korean J Food & Nutr 12: 1-6.   과학기술학회마을
23 Youn KC, Kim DH, Kim JO, Park BJ, Yook HS, Cho JM, Byun MW. 2002. Quality characteristics of the chungkookjang fermented by the mixed culture of Bacillus natto and B. licheniformis. J Korean Soc Food Sci Nutr 31: 204-210.   과학기술학회마을   DOI   ScienceOn
24 Kim J, Yoo S, Choe J, Park HJ, Hong S, Chang C. 1998. Physicochemical properties of traditional Chonggugjang produced in different regions. Agric Chem Biotechnol 41: 377-383.   과학기술학회마을
25 Lee KH, Rye SH, Lee YS, Kim YM, Moon GS. 2005. Changes of antioxidative activity and related compounds on the Chungkukjang preparation by adding drained boiling water. Korean J Food Cookery Sci 21: 163-170.   과학기술학회마을
26 Choi YB, Sohn HS. 1998. Isoflavone content in Korean fermented and unfermented soybean foods. Korean J Food Sci Technol 30: 745-750.   과학기술학회마을
27 Chung WY, Kim SK, Son JY. 2008. Isoflavones contents and physiological activities of soybeans fermented with Aspergillus oryzae or Bacillus natto. J Korean Soc Food Sci Nutr 37: 141-147.   과학기술학회마을   DOI   ScienceOn
28 Potter SM, Baum JA, Teng H, Stillman RJ, Shay NF, Erdman JW Jr. 1998. Soy protein and isoflavones: their effects on blood lipids and bone density in postmenopausal women. Am J Clin Nutr 68: 1375S-1379S.   DOI
29 Alekel DL, Germain AS, Peterson CT, Hanson KB, Stewart JW, Toda T. 2000. Isoflavone-rich soy protein isolate attenuates bone loss in the lumbar spine of perimenopausal women. Am J Clin Nutr 72: 844-852.   DOI
30 Tsuchida K, Mizushima S, Toba M, Soda K. 1999. Dietary soybeans intake and bone mineral density among 995 middle-aged women in Yokohama. J Epidemiol 9: 14-19.
31 Masilamani M, Wei J, Sampson HA. 2012. Regulation of the immune response by soybean isoflavones. Immunol Res 54: 95-110.   DOI   ScienceOn
32 Baeza I, De Castro NM, Arranz L, De la Fuente M. 2010. Soybean and green tea polyphenols improve immune function and redox status in very old ovariectomized mice. Rejuvenation Res 13: 665-674   DOI   ScienceOn
33 Kim JI, Kang MJ, Kwon TW. 2003. Antidiabetic effect of soybean and Chongkukjang. Korea Soybean Digest 20: 44-52.
34 Makino T, Ono T, Muso E, Honda G. 1998. Inhibitory effect of Perilla frutescens and its phenolic constituents on cultured murine mesangial cell proliferation. Planta Med 64: 541-545.   DOI   ScienceOn
35 Coligan EJ, Kruisbeek MA, Margulies HD, Shevach ME, Strober W. 1993. Current protocols in immunology. Wiley Interscience, New York, NY, USA. p 532-534.
36 Kurachi H, Adachi H, Ohtsuka S, Morishige K, Amemiya K, Keno Y, Shimomura I, Tokunaga K, Miyake A, Matsuzawa Y. 1993. Involvement of epidermal growth factor in inducing obesity in ovariectomized mice. Am J Physiol 265: E323-E231.
37 Lee DJ, Kim SM. 2001. Correlation of the bone mineral density and weight reduction therapy in estrogen replaced obese postmenopausal women. Korean J Obes 10: 306-313.
38 Bray GA. 1992. Genetic, hypothalamic and endocrine features of clinical and experimental obesity. Prog Brain Res 93: 333-340.   DOI
39 Lorden JF, Caudle A. 1986. Behavioral and endocrinological effects of single injections of monosodium glutamate in the mouse. Neurobehav Toxicol Teratol 8: 509-519.
40 Wegorzewska IN, Walters K, Weiser MJ, Cruthirds DF, Ewell E, Larco DO, Handa RJ, Wu TJ. 2008. Postovariectomy weight gain in female rats is reversed by estrogen receptor ${\alpha}$ agonist, propylpyrazoletriol. Am J Obstet Gynecol 199: e1-e5.   DOI   ScienceOn
41 Turcato E, Zamboni M, De Pergola G, Armellini F, Zivelonghi A, Bergamo-Andreis IA, Giorgino R, Bosello O. 1997. Interrelationships between weight loss, body fat distribution and sex hormones in pre- and postmenopausal obese women. J Intern Med 241: 363-372.   DOI   ScienceOn
42 Haffner SM, Katz MS, Dunn JF. 1991. Increased upper body and overall adiposity is associated with decreased sex hormone binding globulin in postmenopausal women. Int J Obes 15: 471-478.
43 Lee MR, Park MN, Mun JY, Lee YS. 2011. Effects of a low calcium diet and oxalate intake on calcium deposits in soft tissues and bone metabolism in ovariectomized rats. Korean J Nutr 44: 101-111.   과학기술학회마을   DOI   ScienceOn
44 Effros RB. 2004. Replicative senescence of CD8 T cells: effect on human ageing. Exp Gerontol 39: 517-524.   DOI   ScienceOn
45 Arron JR, Choi Y. 2000. Bone versus immune system. Nature 408: 535-536.   DOI   ScienceOn
46 John V, Hock JM, Short LL, Glasebrook AL, Galvin RJ. 1996. A role for CD8+ T lymphocytes in osteoclast differentiation in vitro. Endocrinology 137: 2457-2463.   DOI
47 Roggia C, Gao Y, Cenci S, Weitzmann MN, Toraldo G, Isaia G, Pacifici R. 2001. Up-regulation of TNF-producing T cells in the bone marrow: a key mechanism by which estrogen deficiency induces bone loss in vivo. Proc Natl Acad Sci U S A 98: 13960-13965.   DOI   ScienceOn
48 Weitzmann MN, Cenci S, Rifas L, Brown C, Pacifici R. 2000. Interleukin-7 stimulates osteoclast formation by upregulating the T-cell production of soluble osteoclastogenic cytokines. Blood 96: 1873-1878.
49 Buchinsky FJ, Ma Y, Mann GN, Rucinski B, Bryer HP, Romero DF, Jee WS, Epstein S. 1996. T lymphocytes play a critical role in the development of cyclosporin A-induced osteopenia. Endocrinology 137: 2278-2285.   DOI
50 Pietschmann P, Grisar J, Thien R, Willheim M, Kerschan- Schindl K, Preisinger E, Peterlik M. 2001. Immune phenotype and intracellular cytokine production of peripheral blood mononuclear cells from postmenopausal patients with osteoporotic fractures. Exp Gerontol 36: 1749-1759.   DOI   ScienceOn
51 Teitelbaum SL. 2004. Postmenopausal osteoporosis, T cells, and immune dysfunction. Proc Natl Acad Sci U S A 101: 16711-16712.   DOI   ScienceOn
52 Jilka RL. 1998. Cytokines, bone remodeling, and estrogen deficiency: a 1998 update. Bone 23: 75-81.   DOI   ScienceOn
53 Pacifici R. 1998. Cytokines, estrogen, and postmenopausal osteoporosis-the second decade. Endocrinology 139: 2659-2661.   DOI
54 Manolagas SC. 1995. Role of cytokines in bone resorption. Bone 17: 63S-67S.   DOI   ScienceOn