Preventive Effect of Epigallocatechin Gallate, the Main Component of Green Tea, on Acute Lung Injury Caused by Air Pollutants

Biomolecules. 2022 Aug 29;12(9):1196. doi: 10.3390/biom12091196.

Abstract

Reducing the health hazards caused by air pollution is a global challenge and is included in the Sustainable Development Goals. Air pollutants, such as PM2.5, induce respiratory and cardiovascular disorders by causing various inflammatory responses via oxidative stress. Catechins and polyphenols, which are components of green tea, have various protective effects, owing to their antioxidant ability. The main catechin in green tea, epigallocatechin gallate (EGCG), is potentially effective against respiratory diseases, such as idiopathic pulmonary fibrosis and asthma, but its effectiveness against air-pollution-dependent lung injury has not yet been investigated. In this study, we examined the effect of EGCG on urban aerosol-induced acute lung injury in mice. Urban aerosol treatment caused increases in inflammatory cell counts, protein levels, and inflammatory cytokine expression in the lungs of ICR mice, but pretreatment with EGCG markedly suppressed these responses. Analyses of oxidative stress revealed that urban aerosol exposure enhanced reactive oxygen species (ROS) production and the formation of ROS-activated neutrophil extracellular traps (NETs) in the lungs of mice. However, ROS production and NETs formation were markedly suppressed by pretreating the mice with EGCG. Gallocatechin gallate (GCG), a heat-epimerized form of EGCG, also markedly suppressed urban aerosol-dependent inflammatory responses and ROS production in vivo and in vitro. These findings suggest that EGCG and GCG prevent acute lung injury caused by urban aerosols through their inhibitory effects on ROS production. Thus, we believe that foods and medications containing EGCG or GCG may be candidates to prevent the onset and progression of acute lung injury caused by air pollutants.

Keywords: air pollution; epigallocatechin gallate; neutrophil extracellular traps; oxidative stress; reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury* / chemically induced
  • Acute Lung Injury* / drug therapy
  • Air Pollutants* / toxicity
  • Animals
  • Antioxidants / pharmacology
  • Catechin* / analogs & derivatives
  • Catechin* / pharmacology
  • Catechin* / therapeutic use
  • Cytokines
  • Mice
  • Mice, Inbred ICR
  • Particulate Matter / toxicity
  • Reactive Oxygen Species / metabolism
  • Respiratory Aerosols and Droplets
  • Tea

Substances

  • Air Pollutants
  • Antioxidants
  • Cytokines
  • Particulate Matter
  • Reactive Oxygen Species
  • Tea
  • Catechin
  • epigallocatechin gallate

Grants and funding

This study was funded primarily by ITO EN, Ltd. (Ken2009-03), Tokyo, Japan. The study was also partially supported by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (Kakenhi Kiban (C) 22K06588).