Effect of PEA on LPS inflammatory action in human adipocytes

Cytokine. 2006 Jun;34(5-6):291-6. doi: 10.1016/j.cyto.2006.06.005. Epub 2006 Aug 1.

Abstract

N-Palmitoylethanolamide (PEA) is an endogenous lipid secreted by human adipocytes that possesses numerous anti-inflammatory properties. Human adipose tissue can be subjected to modulation of its inflammatory state by lipopolysaccharide (LPS). Here we demonstrate that LPS increases the secretion of interleukin-6 (IL-6) by human mature adipocytes via activation of the NFkappaB pathway. This effect is not inhibited by PEA. Inversely, LPS strongly inhibits adipose cell leptin release, with PEA acting as a potentiator of this inhibitory effect. These actions are not linked to a reduction in leptin gene transcription. Thus, PEA does not have an anti-inflammatory role in the secretion of IL-6 via NFkappaB at the adipocyte level, but instead seems to act at the heart of the LPS-stimulated pathway, which, independently of NFkappaB, inhibits the secretion of leptin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Adult
  • Amides
  • Cells, Cultured
  • Endocannabinoids
  • Ethanolamines
  • Humans
  • Inflammation / chemically induced
  • Interleukin-6 / metabolism
  • Leptin / metabolism
  • Lipopolysaccharides / pharmacology*
  • Middle Aged
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / metabolism
  • Palmitic Acids / pharmacology*

Substances

  • Amides
  • Endocannabinoids
  • Ethanolamines
  • Interleukin-6
  • Leptin
  • Lipopolysaccharides
  • NF-kappa B
  • Palmitic Acids
  • palmidrol