Inhibition of arsenite-induced apoptosis and AP-1 activity by epigallocatechin-3-gallate and theaflavins

J Environ Pathol Toxicol Oncol. 2000;19(3):287-95.

Abstract

Arsenite-induced apoptosis appears to be important in its toxicity and its role in carcinogenesis. Green tea has been used as a traditional Chinese remedy for detoxification of arsenite-caused toxicity. In the present work, we found that tea polyphenols, EGCG and theaflavins, effectively blocked arsenite-induced apoptosis of JB6 cells and inhibited arsenite-induced AP-1 transcription activity and AP-1 DNA binding activity. EGCG and theaflavins potently inhibited arsenite-induced Erks activity, but not p38 kinase activity. PD 98059, an inhibitor of Erks, and DNM-JNK1 blocked arsenite-induced apoptosis, while SB202190, an inhibitor of p38 kinases, or DNM-p38 kinase did not. We conclude that Erks and JNKs may be involved in arsenite-induced apoptosis, and the inhibition of arsenite-induced apoptosis by EGCG and theaflavins may be mediated by a decreased phosphorylation of Erks and JNKs. Furthermore, these results provide a possible mechanism for the detoxification effect of tea on arsenite-induced toxicity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antimutagenic Agents / pharmacology*
  • Antioxidants / pharmacology*
  • Apoptosis / drug effects*
  • Arsenites / antagonists & inhibitors*
  • Arsenites / toxicity
  • Biflavonoids*
  • Catechin / analogs & derivatives
  • Catechin / pharmacology*
  • Cells, Cultured
  • DNA / metabolism
  • Drug Interactions
  • Flavonoids / pharmacology
  • Imidazoles / pharmacology
  • JNK Mitogen-Activated Protein Kinases
  • MAP Kinase Signaling System / drug effects
  • Mice
  • Mitogen-Activated Protein Kinase Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism
  • Phenols / pharmacology
  • Phosphorylation
  • Polymers / pharmacology
  • Pyridines / pharmacology
  • Skin / cytology
  • Skin / drug effects
  • Skin / metabolism
  • Tea
  • Teratogens / toxicity*
  • Transcription Factor AP-1 / biosynthesis
  • Transcription Factor AP-1 / metabolism*
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Antimutagenic Agents
  • Antioxidants
  • Arsenites
  • Biflavonoids
  • Flavonoids
  • Imidazoles
  • Phenols
  • Polymers
  • Pyridines
  • Tea
  • Teratogens
  • Transcription Factor AP-1
  • theaflavin
  • Catechin
  • DNA
  • epigallocatechin gallate
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinase Kinases
  • arsenite
  • 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one