Hepatoprotective phytocompounds from Cryptomeria japonica are potent modulators of inflammatory mediators

Phytochemistry. 2008 Apr;69(6):1348-58. doi: 10.1016/j.phytochem.2008.01.017. Epub 2008 Mar 6.

Abstract

Cryptomeria japonica is an important plantation conifer tree in Asia. This study aimed to characterize the anti-inflammatory and hepatoprotective activities of the phytocompounds from C. japonica wood on LPS- or TPA-induced activation of proinflammatory mediators and CCl(4)-induced acute liver injury in mice. A CJH7-2 fraction was purified from C. japonica extracts following bioactivity-guided fractionation, and it exhibited significant activities on inhibition of NO production and iNOS expression as well as up-regulating HO-1 expression in LPS-stimulated macrophages. CJH7-2 also potently inhibits COX-2 enzymatic activity (IC(50)=5 microg/mL) and TPA-induced COX-2 protein expression in mouse skin (1mg/200 microL/site). CJH7-2 (10 mg/kg BW) can prevent CCl(4)-induced liver injury and aminotransferases activities in mice. Chemical fingerprinting analysis showed that terpenes are the major bioactive compounds in the CJH7-2 fraction. This is the first study to demonstrate that chemical constituents from the wood extract of C. japonica possess anti-inflammatory activities in vitro and in vivo that may play a role in hepatoprotection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon Tetrachloride / toxicity
  • Cell Line
  • Chemical and Drug Induced Liver Injury
  • Cryptomeria / chemistry*
  • Cyclooxygenase Inhibitors / chemistry*
  • Cyclooxygenase Inhibitors / pharmacology*
  • Female
  • Inflammation / drug therapy
  • Liver Diseases / drug therapy
  • Macrophages / drug effects
  • Male
  • Mice
  • Mice, Inbred ICR
  • Molecular Structure
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Skin / drug effects
  • Skin / metabolism
  • Terpenes / chemistry*
  • Terpenes / pharmacology*
  • Wood / chemistry

Substances

  • Cyclooxygenase Inhibitors
  • Terpenes
  • Carbon Tetrachloride
  • Prostaglandin-Endoperoxide Synthases