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The Therapeutic Effects of Korean Red Ginseng on Carbon Tetrachloride- and Galactosamine-induced Hepatotoxicity in Rats

홍삼의 사염화탄소 및 갈락토사민 유발 간독성에 대한 치료효과

  • Published : 2003.03.01

Abstract

In this study, we investgated the effect of Red Ginseng (KRG) on liver damage induced by carbon tetrachloride (CTC) and galactosamine (GalN) in rats using indicator enzymes such as serum alanine/aspartate aminotransferases, sorbital dehydrogenase, lactate dehydrogenase, and ${\gamma}$-glutamyltransferase. Treatment of KRG restored these enzyme activities to near normal level compared to CTC or GalN treatment alone. Treatment of KRG also enhanced hepatic microsomal enzyme system, malondialdehyde formation, and depletion of reduced glutathione content, which were reduced by CTC or GalN. We also found that the decreased activities of glutathione S-transferase and glutathine reductase but not ${\gamma}$-glutamycysteine synthetase after KRG treatment restored to normal level. These results indicate that KRG has potent therapeutic activity against CTC- and GalN-induced hepatotoxicity in rat.

Keywords

References

  1. Campos, R, Garrido, A., Guerra, R. and Valenzuela, A.: Planta Medica, 55, 417-419 (1989) https://doi.org/10.1055/s-2006-962055
  2. Martindale, ?.: The Extra Pharmacopoeia, The Pharmaceutical Press, p.1631 (1989)
  3. 이정규,김나영,한용남,최종원 : 고려인삼학회지,26,투고 중 (2002)
  4. Lowry, O. H., Rodebrough, N. J. Farr, A. L. and Randall, R. J.: J. Biol. Chem., 193, 265 (1951)
  5. Reitman, S. and Frankel, S. K: Amer. J. Clin. Pathol., 28, 56 (1957)
  6. Weisner, I. S., Rawnsley, H. M., Brooks, F. P. and Senior, J. R.: Am. J. Dig. Dis., 10, 147 (1965) https://doi.org/10.1007/BF02236665
  7. Szasa, F: Clin. Chem., 15, 124 (1969)
  8. Kind, P. R. N. and King, E. J.: J. Clin. Pathol., 7, 322 (1954) https://doi.org/10.1136/jcp.7.4.322
  9. Berga, L. and Btoida, D.: Sigma Tech. Bull., 500-8-60 (1960)
  10. Ohkawa, H., Ohishi, N. and Yaki, K.: Anal. Biochem., 95, 351 (1979) https://doi.org/10.1016/0003-2697(79)90738-3
  11. Omura, T. and Sato, R.: J. Biol. Chem., 239, 2370 (1964)
  12. Bidlack, W. R. and Lowry, G. L.: Biochem. Pharmacol., 31, 311 (1982) https://doi.org/10.1016/0006-2952(82)90176-9
  13. Nash, T.: J. Biol. Chem., 55, 416 (1953)
  14. Habig, W. H., Pabist, M. J. and Jakoby, W. B.: J. Biol. Chem., 249, 7130 (1974)
  15. Richardson, R. J. and Murphy, S. D.: Toxicol. Appl. Pharmacol., 31, 505 (1975) https://doi.org/10.1016/0041-008X(75)90274-4
  16. Summer, K. H. and Greim, H.: Biochem. Biophys. Res. Commun., 96, 566 (1980) https://doi.org/10.1016/0006-291X(80)91393-5
  17. Mize, C. E. and Langdon, R. G.: J. Biol. Chem., 237, 1589 (1962)
  18. Meister, A. and Richman, P. G.: J. Biol. Chem., 250, 1422 (1975)
  19. Klassen, C. D. and Fitzgerraid, T. J.: J. Pharmacol. Exp. Ther., 191, 548(1974)
  20. Ahokas, J. T., Nichollas, F. A., Ravenscroft, P. J. and Emmerson, B. T.: Biochem. Pharmacol., 34, 2157 (1985) https://doi.org/10.1016/0006-2952(85)90411-3