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Effects of volatile constituents of rosemary extract on lung inflammation induced by diesel exhaust particles.

Abstract
Epidemiological and experimental studies have implicated that diesel exhaust particles are involved in increases in morbidity and mortality from lung diseases. Recently, we have demonstrated that rosmarinic acid, a polyphenolic liquid component in perilla, inhibits lung inflammation induced by diesel exhaust particles in vivo, partly through its antioxidative property. We have also shown the antioxidative activities of volatile constituents of rosemary extract, the gaseous component in perilla, in vitro. The purpose of this study was to evaluate the effects of intratracheal administration of volatile rosemary extract on lung inflammation induced by diesel exhaust particles. ICR mice were treated with intratracheal administration of volatile rosemary extract before intratracheal exposure to diesel exhaust particles. Twenty-four hr later, diesel exhaust particles exposure elicited lung inflammation characterized by the infiltration of neutrophils and eosinophils, which was confirmed by cellular profile of bronchoalveolar lavage fluid and histological examination. Diesel exhaust particles enhanced the protein expressions of interleukin-1beta, macrophage inflammatory protein-1alpha, macrophage chemoattractant protein-1, and keratinocyte chemoattractant in the lung. Pretreatment with rosemary extract significantly inhibited the diesel exhaust particles-induced lung inflammation. Rosemary extract treatment also suppressed the diesel exhaust particles-enhanced lung expression of macrophage inflammatory protein-1alpha, macrophage chemoattractant protein-1, and keratinocyte chemoattractant. These results suggest that intratracheal administration of rosemary extract can prevent lung inflammation induced by diesel exhaust particles. The preventive effect is mediated, at least partly, through the inhibition of the enhanced lung expressions of macrophage inflammatory protein-1alpha, macrophage chemoattractant protein-1, and keratinocyte chemoattractants.
AuthorsKen-ichiro Inoue, Hirohisa Takano, Akira Shiga, Yoji Fujita, Hiroaki Makino, Rie Yanagisawa, Yoji Kato, Toshikazu Yoshikawa
JournalBasic & clinical pharmacology & toxicology (Basic Clin Pharmacol Toxicol) Vol. 99 Issue 1 Pg. 52-7 (Jul 2006) ISSN: 1742-7835 [Print] England
PMID16867171 (Publication Type: Journal Article)
Chemical References
  • Chemokines
  • Cytokines
  • Interleukin-1
  • Plant Extracts
  • Vehicle Emissions
Topics
  • Administration, Inhalation
  • Animals
  • Bronchoalveolar Lavage Fluid (cytology)
  • Chemokines (biosynthesis)
  • Cytokines (biosynthesis)
  • Eosinophils
  • Interleukin-1 (metabolism)
  • Ledum (chemistry)
  • Leukocyte Count
  • Lung (drug effects, metabolism, pathology)
  • Male
  • Mice
  • Mice, Inbred ICR
  • Neutrophil Infiltration (drug effects)
  • Neutrophils
  • Plant Extracts (chemistry, pharmacology)
  • Pneumonia (chemically induced, pathology, prevention & control)
  • Vehicle Emissions (toxicity)
  • Volatilization

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