In vitro and in vivo anti-inflammatory effects of ethanol extract from Acer tegmentosum

J Ethnopharmacol. 2010 Mar 2;128(1):139-47. doi: 10.1016/j.jep.2009.12.042. Epub 2010 Jan 4.

Abstract

Aim of study: Acer tegmentosum has been traditionally used for folk medicine to treat hepatic disorders such as hepatitis, hepatic cancer, and hepatic cirrhosis. In this study, we demonstrate the ethno-pharmacological activity of Acer tegmentosum in in vitro and in vivo inflammatory conditions.

Results: The 70% ethanol extract (At-EE) of Acer tegmentosum dose-dependently diminished the production of nitric oxide (NO), tumour necrosis factor (TNF)-alpha, and prostaglandin (PG)E(2), in lipopolysaccharide (LPS)-activated RAW264.7 cells and peritoneal macrophages, by a transcriptional mechanism. At-EE also suppressed the activation of nuclear factor (NF)-kappaB, activator protein (AP)-1, and cAMP-responsive element binding (CREB), and simultaneously blocked their upstream inflammatory signalling cascades, including Akt, p38, and JNK. Furthermore, At-EE protected against LPS-induced cell death induced by reactive oxygen species (ROS) and reactive nitrogen species (RNS) and neutralized reactive species generation. In agreement with the in vitro results, orally administered At-EE strongly ameliorated ear oedema formation induced by arachidonic acid.

Conclusion: At-EE displays strong anti-inflammatory activities in vitro and in vivo, contributing to its major ethno-pharmacological role such as anti-hepatitis remedy and may be applicable to novel anti-inflammatory therapeutics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acer / chemistry*
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Arachidonic Acid / pharmacology
  • Base Sequence
  • Cell Line
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • DNA Primers
  • Dinoprostone / biosynthesis
  • Ethanol / chemistry*
  • Humans
  • In Vitro Techniques
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NF-kappa B
  • Nitric Oxide / biosynthesis
  • Plant Extracts / pharmacology*
  • Reactive Oxygen Species / metabolism
  • Transcription Factor AP-1 / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Anti-Inflammatory Agents
  • Cyclic AMP Response Element-Binding Protein
  • DNA Primers
  • NF-kappa B
  • Plant Extracts
  • Reactive Oxygen Species
  • Transcription Factor AP-1
  • Tumor Necrosis Factor-alpha
  • Arachidonic Acid
  • Nitric Oxide
  • Ethanol
  • Dinoprostone