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  • 标题:Inhibitory Effects of Conjugated Epicatechin Metabolites on Peroxynitrite-mediated Nitrotyrosine Formation
  • 本地全文:下载
  • 作者:Midori Natsume ; Naomi Osakabe ; Akiko Yasuda
  • 期刊名称:Journal of Clinical Biochemistry and Nutrition
  • 印刷版ISSN:0912-0009
  • 电子版ISSN:1880-5086
  • 出版年度:2008
  • 卷号:42
  • 期号:1
  • 页码:50-53
  • DOI:10.3164/jcbn.2008008
  • 出版社:The Society for Free Radical Research Japan
  • 摘要:Previously, we identified four metabolites of (−)-epicatechin in blood and urine: (−)-epicatechin-3'- O -glucuronide (E3'G), 4'- O -methyl-(−)-epicatechin-3'- O -glucuronide (4'ME3'G), (−)-epicatechin-7- O -glucuronide (E7G), and 3'- O -methyl-(−)-epicatechin-7- O -glucuronide (3'ME7G) (Natsume et al. Free Radical Biol. Med. 34, 840-849, 2003). The aim of the current study was to compare the antioxidative activities of these metabolites with that of their parent compound. After oral administration of (−)-epicatechin, E3'G and 4'ME3'G were isolated from human urine, and E7G and 3'ME7G isolated from rat urine. We found that these compounds inhibited peroxynitrite-mediated tyrosine nitration, in the following order of potency: E3'G > (−)-epicatechin > E7G = 3'ME7G. = 4'ME3'G. These results demonstrate that the metabolites of (−)-epicatechin retain antioxidative activity on peroxynitrite-induced oxidative damages to some extent.
  • 关键词:(−)-epicatechin;glucuronide;metabolites;peroxynitrite;nitrotyrosine
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