Comparative Study of 3 kinds of Black Soybean on Murine Immune Cells

생쥐의 면역세포에 대한 검은콩 3종의 비교 연구

  • Received : 2010.07.13
  • Accepted : 2010.07.30
  • Published : 2010.08.25

Abstract

The purpose of this research was the comparative study of 3 kinds of black soybean on murine immune cells. The 3 kinds of black soybean are Glycine max Merr. with inner color-yellow (GY), Glycine max Merr. with inner color-greenish (GG) and Rhynchosia volubilis Lour. (RV). All of the black soybean increased the viability of murine thymocytes in vitro. The combined treatment of GY or GG and mitogen did not affect the viability of splenic T- and B-lymphocytes compared with mitogen-treated group, but the combined treatment of RV and mitogen increased their action compared with mitogen-treated group. Also, the 3 kinds of black soybean were given p.o. once a day for 7 days, respectively. RV increased the population of thymic-$CD8^+$, splenic-$CD8^+$ and $B220^+$ cells in vivo. Furthermore, GY and GG did not affect the phagocytic activity and the production of nitric oxide in peritoneal macrophages in vitro, but RV enhanced their action. These results suggest that immunopotentiative action of Rhynchosia volubilis Lour. is more potent than their of Glycine max Merr.

Keywords

References

  1. 李時珍. 本草綱目. 北京, 人民衛生出版社, p 1501, 1982.
  2. 김창민 외. 완역중약대사전. 도서출판정담, p 1014, 6635, 1997.
  3. 許浚. 東醫寶鑑. 서울, 南山堂, p 589, 1987.
  4. Sakai, T. and Kogiso, M. Soy isoflavones and immunity. J. Med. Invest., 55: 167-173, 2008. https://doi.org/10.2152/jmi.55.167
  5. Wu, D., Meydani, M., Leka, L.S., Nightingale, Z., Handelman, G.J., Blumberg, J.B., Meydani, S.N. Effect of dietary supplementation with black currant seed oil on the immune response of healthy elderly subjects. Am. J. Clin. Nutr., 70(4):536-543, 1999. https://doi.org/10.1093/ajcn/70.4.536
  6. Cassileth, B.R., Vickers, A.J. Soy: an anticancer agent in wide use despite some troubling data. Cancer Invest., 21(5):817-818, 2003. https://doi.org/10.1081/CNV-120023782
  7. Maeda, H., Katsuki, T., Akaike, T., Yasutake, R. High correlation between lipid peroxide radical and tumor-promoter effect: suppression of tumor promotion in the Epstein-Barr virus/B-lymphocyte system and scavenging of alkyl peroxide radicals by various vegetable extracts. Jpn. J. Cancer Res., 83(9):923-928, 1992. https://doi.org/10.1111/j.1349-7006.1992.tb02001.x
  8. Liao, H.F., Chou, C.J., Wu, S.H., Khoo, K.H., Chen, C.F., Wang, S.Y. Isolation and characterization of an active compound from black soybean [Glycine max (L.) Merr.] and its effect on proliferation and differentiation of human leukemic U937 cells. Anticancer Drugs. 12(10):841-846,2001. https://doi.org/10.1097/00001813-200111000-00008
  9. Jang, E.H., Moon, J.S., Ko, J.H., Ahn, C.W., Lee, H.H., Shin, J.K., Park, C.S., Kang, J.H. Novel black soy peptides with antiobesity effects: activation of leptin-like signaling and AMP-activated protein kinase. Int. J. Obes. (Lond). 32(7):1161-1170, 2008. https://doi.org/10.1038/ijo.2008.60
  10. Kim, H.J., Bae, I.Y., Ahn, C.W., Lee, S., Lee, H.G. Purification and identification of adipogenesis inhibitory peptide from black soybean protein hydrolysate. Peptides. 28(11):2098-2103, 2007. https://doi.org/10.1016/j.peptides.2007.08.030
  11. Zhao, Q.W., Lou, Y.J. Estrogenic activity and its mechanism of ethanol extract from black soybean. Zhongguo Zhong Yao Za Zhi. 31(10):825-828, 2006.
  12. Takahashi, R., Ohmori, R., Kiyose, C., Momiyama, Y., Ohsuzu, F., Kondo, K. Antioxidant activities of black and yellow soybeans against low density lipoprotein oxidation. J. Agric. Food Chem., 53(11):4578-4582, 2005. https://doi.org/10.1021/jf048062m
  13. Yamai, M., Tsumura, K., Kimura, M., Fukuda, S., Murakami, T., Kimura, Y. Antiviral activity of a hot water extract of black soybean against a human respiratory illness virus. Biosci. Biotechnol. Biochem., 67(5):1071-1079, 2003.
  14. Sakai, T., Kogiso, M. Soy isoflavones and immunity. J. Med. Invest., 55(3-4):167-173, 2008. https://doi.org/10.2152/jmi.55.167
  15. Chan, Y.C., Wu, C.C., Chan, K.C., Lin, Y.G., Liao, J.W., Wang, M.F., Chang, Y.H., Jeng, K.C. Nanonized black soybean enhances immune response in senescenceaccelerated mice. Int. J. Nanomedicine. 4: 27-35, 2009.
  16. Wysocki, L.J. and Sato, V.L. Planning for lymphocytes: A method for cell selection. Proc. Natl. Acad. Sci. USA. 75: 2844, 1978. https://doi.org/10.1073/pnas.75.6.2844
  17. Mizel, S.B., Openheim, J.J. and Rosensteich, D.L. Characterization of lymphocyte-activating factor(LAF) produced by the macrophage cell line P388D1. J. Immunol. 120: 1497, 1979.
  18. Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxic assays. J. Immunol. methods. 65: 55, 1983. https://doi.org/10.1016/0022-1759(83)90303-4
  19. Kotnic, V. and Fleischmann, W.R.Jr. A simple and rapid method to determine hematopoietic growth factor activity. J. Immunol. methods. 129: 23, 1990. https://doi.org/10.1016/0022-1759(90)90416-S
  20. Suda, T. and Nagata, S. Purification and characterization of the Fas-ligand that induces apoptosis. J. Exp. Med., 179: 873-879, 1994. https://doi.org/10.1084/jem.179.3.873
  21. Boudard, F., Vallot, N., Cabaner, C. and Bastide, M. Chemiluminenscence and nitrite determinations by the MALU macrophage cell line. J. Immunol. Methods, 174: 259, 1994. https://doi.org/10.1016/0022-1759(94)90030-2
  22. Blair, A.L., Cree, I.A., Beck, J.S. and Hating, M.J.G. Measurement of phagocyte chemiluminenscence in a microtiter plate format. J. Immunol. Methods, 112: 163, 1988. https://doi.org/10.1016/0022-1759(88)90352-3
  23. Rockett, K.A., Awburn, M.M., Cowden, W.B. and Clark, I.A. Killing of Plasmodium faciparum in vitro by nitric oxide derivatives. Infec. Immunity, 59(9):3280, 1991.
  24. Seo, S.Y., Pang, J., Li, R.H., Kwon, J., Ahn, M.S. and Eun, J.S. Effects of the Combined Extracts of Glycine Max Merr. and Glycyrrhiza Uralensis on the Activity of Murine Splenocytes and Macrophages. Kor. J. Oriental Physiology & Pathology, 23(6):1385-1391, 2009
  25. Miceli, M.C. and Parnes, J.R. The role of CD4 and CD8 in T cell activation and differentiation. Advances in Immunology, 53: 59, 1993. https://doi.org/10.1016/S0065-2776(08)60498-8
  26. Charles, A.J., Paul, T., Mark, W. The immune system in health and disease. 4ed, Garland Pub., p 463, 2000.
  27. Channon, J.Y., Leslie, C.C. and Johnston, Jr.R.B. Zymosan-stimulated production of phosphatidic acid by macrophages: relationship to release of superoxide anion and inhibition by agents that increase intracellular cyclic AMP. J. Leucocyte Biol., 41: 450-455, 1987. https://doi.org/10.1002/jlb.41.5.450