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Inhibition in vitro linoleic acid peroxidation and haemolysis by caffeoyltryptophan.

Abstract
Antioxidant activities of caffeoyltryptophan were investigated by the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging system, the superoxide anion generation system and the superoxide anion-mediated linoleic acid peroxidation system. At 10 microM, caffeoyltryptophan showed greater scavenging activity on DPPH than dl-alpha-tocopherol or ascorbic acid. DPPH radical scavenging activity of caffeoyltryptophan increased dose-dependently at concentrations ranging from 1 to 50 microM; 1 mol of caffeoyltryptophan reacted with ca 4 mol of radical. Caffeoyltryptophan caused 80% inhibition of superoxide anion generation at 50 microM. The inhibitory activity of caffeoyltryptophan was as strong as that of 5-caffeoylquinic acid. Caffeoyltryptophan inhibited the formation of conjugated diene from linoleic acid. The inhibitory activity increased in the order caffeic acid < 5-caffeoylquinic acid < caffeoyltryptophan < dl-alpha-tocopherol. Effects on the in vitro haemolysis and peroxidation of mouse erythrocytes induced by H2O2 were also examined. Caffeoyltryptophan exhibited strong inhibitory activities; Tryptophan was ineffective in these systems. These data suggest that caffeoyltryptophan may be a natural antioxidant in the human diet and, as such, may intervene in toxicological processes that are mediated by radical mechanisms.
AuthorsM Ohnishi, H Morishita, S Toda, Y Yase, R Kido
JournalPhytochemistry (Phytochemistry) Vol. 47 Issue 7 Pg. 1215-8 (Apr 1998) ISSN: 0031-9422 [Print] England
PMID9611825 (Publication Type: Journal Article)
Chemical References
  • Antioxidants
  • Caffeic Acids
  • Free Radical Scavengers
  • caffeoyltryptophan
  • Tryptophan
  • Linoleic Acid
Topics
  • Animals
  • Antioxidants (chemistry, pharmacology)
  • Caffeic Acids (chemistry, pharmacology)
  • Free Radical Scavengers (chemistry, pharmacology)
  • Hemolysis (drug effects)
  • Linoleic Acid (metabolism)
  • Lipid Peroxidation (drug effects)
  • Male
  • Mice
  • Tryptophan (analogs & derivatives, chemistry, pharmacology)

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