Epigallocathechin-3 gallate inhibits cardiac hypertrophy through blocking reactive oxidative species-dependent and -independent signal pathways

Hong Liang Li, Yue Huang, Chan Na Zhang, Guang Liu, Yu Sheng Wei, Ai Bing Wang, Yu Qing Liu, Rui Tai Hui, Chiming Wei, G. Metville Williams, De Pei Liu, Chih Chuan Liang

Research output: Contribution to journalArticlepeer-review

114 Scopus citations


Cardiac hypertrophy is a major cause of morbidity and mortality worldwide. Recent in vitro and in vivo studies have suggested that reactive oxygen species (ROS) may play an important role in cardiac hypertrophy. It was therefore thought to be of particular value to examine the effects of antioxidants on cardiac hypertrophy. Epigallocatechin-3-gallate (EGCG) is a major bioactive polyphenol present in green tea and a potent antioxidant. The current study was designed to test the hypothesis that EGCG inhibits cardiac hypertrophy in vitro and in vivo. In this study, we investigated the effects of EGCG on angiotensin II- (Ang II) and pressure-overload-induced cardiac hypertrophy. Our results showed that EGCG attenuated Ang II- and pressure-overload-mediated cardiac hypertrophy. Both reactive oxygen species generation and NADPH oxidase expressions induced by Ang II and pressure overload were suppressed by EGCG. The increased hypertension by pressure overload was almost completely blocked after EGCG treatment. Further studies showed that EGCG inhibited Ang II-induced NF-κB and AP-1 activation. Inhibition of the activity of NF-κB was through blocking ROS-dependent p38 and JNK signaling pathways, whereas inhibition of AP-1 activation was via blocking EGFR transactivation and its downstream events ERKs/PI3K/Akt/mTOR/p70S6K. The combination of these actions resulted in repressing the reactivation of ANP and BNP, and ultimately preventing the progress of cardiac hypertrophy. These findings indicated that EGCG prevents the development of cardiac hypertrophy through ROS-dependent and -independent mechanisms involving inhibition of different intracellular signaling transductional pathways.

Original languageEnglish (US)
Pages (from-to)1756-1775
Number of pages20
JournalFree Radical Biology and Medicine
Issue number10
StatePublished - May 15 2006
Externally publishedYes


  • EGCG
  • EGFR
  • Free radicals
  • Hypertrophy
  • MAPK
  • Reactive oxygen species
  • Signaling transduction

ASJC Scopus subject areas

  • Biochemistry
  • Physiology (medical)


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