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  • 标题:Silymarin and Its Components Are Inhibitors of β-Glucuronidase
  • 本地全文:下载
  • 作者:DongHyun KIM ; YoungHo JIN ; JongBeak PARK
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:1994
  • 卷号:17
  • 期号:3
  • 页码:443-445
  • DOI:10.1248/bpb.17.443
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:Silymarin, a commercial crude drug used as a hepatoprotective, was found to inhibit 53% of β-glucuronidase activity at a final concentration of 0.8 mg/ml. Of three compounds A, silybin and C, which were isolated from silymarin, A and silybin potently inhibited the enzyme activity, followed by C. β-Glucuronidases of intestinal bacteria, HGU-1 and HGU-2, and E. coli HB101 were noncompetitively inhibited by silybin. β-Glucuronidase of the feces of a healthy human and of a human with colon cancer were also inhibited by silybin, silymarin and saccharic acid 1, 4-lactone at 0.03-0.15 mg/ml. Silymarin and silybin protected the increase in enzyme activity in the serum of the rats treated with CCl4.
  • 关键词:β-glucuronidase;silymarin;silybin;colon cancer;liver;intestinal bacteria
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