Inductive Effect of Scutellariae radix on Glutathione S-Transferase Yc1/2 from Rat Liver

황금이 백서의 간 조직 글루타치온 에스-전이 효고 Ycl/2의 발현 효과

  • Kim Young Sook (Department of Biochemistry, School of Medicine, Wonkwang University) ;
  • Kim Dong Hyun (Bioanalysis and Biotransformation Research Center, Korea Institute of Science and Technology) ;
  • Choi Mi Jung (Department of Biochemistry, School of Medicine, Wonkwang University) ;
  • Kim Sung Min (Department of Biochemistry, School of Medicine, Wonkwang University) ;
  • Park Rae Kil (Department of Microbiology and Immunology, School of Medicine, Wonkwang University) ;
  • Kwon Kang Beom (Department of Physiology, College of Oriental Medicine, Wonkwang University) ;
  • Ryu Do Gon (Department of Physiology, College of Oriental Medicine, Wonkwang University) ;
  • Kim Bok Ryang (Department of Biochemistry, School of Medicine, Wonkwang University)
  • 김영숙 (원광대학교 의과대학 생화학교실) ;
  • 김동현 (한국과학기술연구원 생체대사 연구센터) ;
  • 최미정 (원광대학교 의과대학 생화학교실) ;
  • 김성민 (원광대학교 의과대학 생화학교실) ;
  • 박래길 (원광대학교 의과대학 미생물학교실) ;
  • 권강범 (원광대학교 한의과대학 생리학교실) ;
  • 류도곤 (원광대학교 한의과대학 생리학교실) ;
  • 김복량 (원광대학교 의과대학 생화학교실)
  • Published : 2003.12.01

Abstract

The water extract of Scutellariae radix was treated to rat and the primary culture of hepatocytes, and the expressions of several glutathione S-transferase (GST) isozymes and the activity of GST Yc1/2 were investigated by Western blot and by the use of HPLC. The results were obtained as follows: The water extract of Scutellariae radix did not induce the expressions of cytosolic GST Ya and GST Yp in rat livers. But, the extract increased the expression of cytosolic GST Yc1/2 to 2-4 fold higher than control. The expression of GST Yc1/2 in the primary culture of rat hepatocytes was induced by the water extract of Scutellariae radix in a dose-dependent manner, reaching 21-fold over control with 50 ㎍/㎖ treatment. The induction of the expression of GST Yc1/2 in rat livers increased the formation of AFB₁-glutathione conjugate from AFB₁-8,9-epoxide which was made in the metabolism of AFB₁.

Keywords

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