Inhibition of neuroinflammation by cinnamon and its main components

Food Chem. 2013 Jun 15;138(4):2275-82. doi: 10.1016/j.foodchem.2012.12.020. Epub 2012 Dec 28.

Abstract

Uncontrolled activation of microglia contributes to neuroinflammation, which is highly involved in the development of neurodegenerative diseases. Although cinnamon has neuro-protective properties, its capacity to inhibit neuroinflammation has not been investigated and its active compounds remain unclear. Therefore, the composition of cinnamon extract was analysed by LC-MS and the ability of cinnamon and its main constituents to inhibit neuroinflammation was evaluated using a lipopolysaccharide (LPS)-activated BV2 microglia culture system. In total, 50 μg/mL cinnamon extract decreased significantly the production and expression of nitric oxide (NO), interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α in LPS-activated BV2 microglia. Blocking of nuclear factor-κB (NF-κB) activation was the most likely mechanism responsible for inhibition by cinnamon of neuroinflammation. Among the eight tested compounds, cinnamaldehyde had the greatest anti-neuroinflammatory capacity. Experimental results suggest that cinnamon may have a potential therapeutic effect against neurodegenerative diseases and its potent anti-neuroinflammatory capacity was primarily attributed to cinnamaldehyde.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cinnamomum zeylanicum / chemistry*
  • Down-Regulation / drug effects*
  • Humans
  • Interleukin-1beta / genetics
  • Interleukin-1beta / immunology
  • Interleukin-6 / genetics
  • Interleukin-6 / immunology
  • Microglia / drug effects
  • Microglia / immunology
  • Neurons / drug effects
  • Neurons / immunology*
  • Neuroprotective Agents / chemistry*
  • Neuroprotective Agents / pharmacology*
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / immunology
  • Plant Extracts / chemistry*
  • Plant Extracts / pharmacology*
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Interleukin-1beta
  • Interleukin-6
  • Neuroprotective Agents
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide Synthase Type II