Free Redical Scavenging and Cytotoxicity Activitives of Soybean Germ Saponin

대두배아 사포닌의 유리기 생성 억제 및 세포독성

  • 류병호 (경성대학교 의용공학부 식품공학과) ;
  • 이홍수 (동부산대학 호텔외식조리과) ;
  • 김현대 (동부산대학 호텔외식조리과)
  • Published : 2002.06.01

Abstract

This study was carried out to investigate functional activities of the free radical scavenging and germ of Glycin max. Merrill fur cytotoxicity toward P338 and L1210 cells derived from mouse. Effect of crude saponin were examined to oxygen radicals and their scavenger enzymes in liver fractions of Spragae-Dawley(SD) rats. Male rats were fed basic diets of control and experiment diets of 0.5∼1.0% crude saponin. There were no significant differences in hydroxy radical($.$OH) formation of liver mitochondria and microsomes in 1.0% group, while $.$OH formations were significantly decrease in 0.5% and 1.0% saponin compared with control group. Their oxygen radical(O$_2$$\^$$.$/) scavenging activities were significantly decrease in liver cytosol of 0.5% and 1.0% saponin group compared with control group. Soybean germ saponin was isolated purified by the method of HPLC to investigate the cytotoxicity of mouse cells by using the MTT assay. SA-1 saponin fraction of soybean germ showed to inhibit toward growth cell of P338 and L1210 cells and its showed less than 50% cytotoxicity These results suggest that the saponin may play a effective role in attenuating a oxygen radical formations and increasing a scavenger enzyme activities.

대두 배아로부터 saponin을 분리.정제하여 유리기 억제효과 및 동물의 암세포에 대한 세포 독성을 조사하였다. 유리기 억제활성에 대한결과를 보면 대두 배아 saponin을 0.5 및 1.0%씩 첨가한 급여 식에서 4주 동안 사육한 후 간장을 절취하여 간장 획분의 활성산소 및 항산화 관련 효소에 대하여 평가하였다. 간장의 mitochondria 및 microtome 획분의 hydroxy radical(.OH)의 생성에 미치는 영향에서 급여식에 사포닌을 첨가한 급여군에서 .OH기의 생성억제 효과를 나타내었다. 간장의 microsome 획 분에서도 0.5 및 1.0% 투여군에서 $H_2O$$_2$생성억제 효과가 인정되었다. 또한 간장의 cytosol획분에서 $O_2$.$^{-}$의 생성은 대조군에 비하여 현저한 억제 효과를 나타내었다. 대두 배아 사포닌의 세포독성을 P338 (mouse Iyoupoid neoplasm)과 L1210 (mouse leukemia) 세포주를 사용하여 실시한 결과 200 $\mu$g/mL 농도에서 높은 성장억제효과를 나타내었다. 그리고 처리 농도에 따른 대두배아 추출물이 P338과 L1210에 대한 성장 효과 실험에서도 200 $\mu$g/mL에서 은 성장억제 효과가 나타났으며 농도가 높을 수록 완전히 억제되는 것을 볼 수 있었다.

Keywords

References

  1. 大久保一良:吉城由美子, 吉城昌樹, 本知玄, 工藤重光:大豆配糖體成分の種類, 構造, 遺伝性, 生理活性:ニューフードインダストリー, 36, 17-27 (1994)
  2. Wang, H. and Murphy, P. A. : Isoflavone composition of American and Japanese soybeans in Iowa, Effects of variety crop tear and location, J. Agric. Food Chem., 42, 1674-1677(1994) https://doi.org/10.1021/jf00044a017
  3. Sharma, O. P., Adlercreutz, H., Strandberg, J. D., Zirkin, B. R., Coffey, D. S. and Ewing, L. L. : Soy of dietary source plays a preventive role against the pathogenesis of prostatitis in rats. J. Steroid Biochem. Mol. Biol., 43, 557-564(1992) https://doi.org/10.1016/0960-0760(92)90244-D
  4. Adlercreutz, H. : Phytoestrogens : Epidemiology and a possible role in cancer protection. Environ. Health Perspect., 103, 103-112(1995) https://doi.org/10.1289/ehp.95103s9103
  5. Aklecreutz, H., Hockerstedt, K., Bannwart, C., Bloigu, S., Hamalainen, E., Fotsis, T. and Ollus, A. : Effect of dietar y components, including lignans and phytoestrogens on sex hormone binding globulin. J. Steroid Biochem., 27. 1135-1144(1987) https://doi.org/10.1016/0022-4731(87)90200-7
  6. Wei, H., Cai, Q. and Rahn, R. : Inhibition of UV light and Feton reaction-induced oxidative DNA damage by the soybean isoflavone genistein. Carcinogenesis, 17, 73(1996) https://doi.org/10.1093/carcin/17.1.73
  7. Messina, M. J., Persky, V., Setchell, K. D. R. and Barnes, S. : Soy intake and cancer risk, a review of in vitro and in vivo data, Nutr. and Cancer, 21, 113-124(1994) https://doi.org/10.1080/01635589409514310
  8. Price, K. R., Johnson, I. T. and Fenwick, C. R. : The chemistry and biological significance of saponins in foods and feeding stuffs. CRC Crit. Rev. Food Sci. Nutr., 26, 27-135(1987) https://doi.org/10.1080/10408398709527461
  9. Shiraiwa, M., Kudou, S., Shimoyamada, M., Harada, K. and Okubo, K. : Composition and structure of 'group A'saponin in soybean seed. Agric. Biol. Chem., 55 (2), 315-22(1991) https://doi.org/10.1271/bbb1961.55.315
  10. Tsukamoto, C., Kikuchi, A., Harada, K., Kitamura, K., Kudoh, S., Wasaki, T. and Okubo, K. : Group A acetyl saponin deficient mutant from the wild soybean. Phytochem., 31 (12), 4913-4142(1988)
  11. Kudou, S., Tonomura, M., Tsukamoto, C., Shmoyamada M., Uchida, T. and Okubo, K. : Isolation and structural elucidation of main genuine soybean saponin. Biosci. Biotech. Biochem., 56(1), 142-143 (1992) https://doi.org/10.1271/bbb.56.142
  12. Tsukamoto, C., Kikuchi, A., Kudou, S., Tonomura, M., Harada, K., Iwasaki, T. and Okubo, K. : Genetic impovement of saponin components in soybean. ACS Symposium seres 546, Food Phytochemicals for Cancer Prevention, American Chemical Society, Washinton DC., USA, pp. 372-379(1994)
  13. 有地泫 :新規サポニン物質, 特許出願公開, 昭 56-64000 (1997)
  14. Yoshicoshi, M., Yoshiki, Y., Okubo,K.,Sato,J.and Sasaki, Y. : Prevention of hydrogen peroxide damage by soybean saponins to mouse fibroflasts, Planta Medica, 6., 252-255(1996)
  15. 有地泫 : 代謝作用薬劑, 特許出願公開, 昭 56-160981 (1980)
  16. Kawano, K., Sato, H. and Sakamura, S. : Isolation and structure of furostanol saponin in asparagus edible shoots. Agric. Biol. Chem., 41, 1-8(1997)
  17. Liu, C. L., Chen, Y. Y., Ge, S. B. and Li, B. G. : Studies on the constituents from Cioscorec plants ll . Isolation and identification of steroidal saponins from Bi'oscoreg cojjeffii Hook F. Tfoxue fuefgo. 18, 597-606(1983)
  18. Shimoyamada, M., Suzuki, M., Sonta, H., Maruyama, M. and Okubo, K. : Antifungal Lctivity of the saponin fraction obtained from Asparagus officinalis L. and its active priciple, Agric. Biol. Chem., 54, 2553-2557(1990) https://doi.org/10.1271/bbb1961.54.2553
  19. Agrwal, P. K., Jain, D. C., Gupta, R. K. and Thakur, R. S. : Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins, Phytochemistry. 24, 2479-2496(1985) https://doi.org/10.1016/S0031-9422(00)80653-6
  20. Bogacheva, N. G., Kiselev, V. P. and Kogan, L. M. : Isolation of 3, 6-bisglycoside of yamogenin from Tgonella foemungaecum. Khim Prir Soedin 268-269(1976)
  21. Lowry, O. H., Roseborough, N. J., Farr, L. A. and Randall, R. J. : Protein measurement with Folin-Phenol reagent. J. Biol. Chem., 193, 265-275(1951)
  22. Halliwell, B. and Gutteridge, J. M. C. : Formation of a thiobarbituric acid-reactive substance from deoxyribose in the persence of iron salts. FEBS Lett., 128, 347-350(1981) https://doi.org/10.1016/0014-5793(81)80114-7
  23. Thurman, F. C., Ley, J. C. and Scholz, R. : Hepatic microsomal ethanol oxidation. Eur. J. Biochem., 25, 420-430(1972) https://doi.org/10.1111/j.1432-1033.1972.tb01711.x
  24. McCord, J. M. and Frdovch, I. : Superoxide dismutase. An enzyme funtion for erythro cuprein(heme cuprein). Chem. J. Biol., 244, 6049-6054(1969)
  25. Charmichael, J., Degroff, W. G., Gazdar, A. F., Minna, J. D. and Michell, J. B : Evalution of a terazolium based semiautonated colorimeteric assay, assessment of chemo sentivity testing, Cancer Res., 47,9366(1987)
  26. 남상해, 양민성 : 산국으로부터 항암활성 성분의 분리, 한국농화학회지, 38, 273(1995)
  27. 이병우, 유익제, 유무영, 황우익, 최춘언 : 초산균체 추출물의 in vitro의 암세포 증식 억제효과, 한국식품과학회지, 27, 445(1995)
  28. 윤기도, 권동진, 홍석찬, 김수일, 정건섭 : 대두 및 대두발효식품의 항돌연변이성, 한국산업미생물학회지(1996)