Docosahexaenoic acid down-regulates endothelial Nox 4 through a sPLA2 signalling pathway

Biochem Biophys Res Commun. 2009 Nov 20;389(3):516-22. doi: 10.1016/j.bbrc.2009.09.013. Epub 2009 Sep 6.

Abstract

We investigated the anti-inflammatory and antioxidant activities of docosahexaenoic acid (DHA) by evaluating its modulation of the two enzymes most involved in vascular inflammation, i.e. endothelial secreted phospholipase A(2) (sPLA(2)) and NADPH oxidase 4 (Nox) 4. Exposure of human aortic endothelial cells (HAECs) to DHA led to its preferential incorporation into outer leaflet phospholipids. Pre-treatment with DHA abolished HAECs stimulation induced by A23187 and Ang II, whereas the effects on IL-1beta treatment were less pronounced. Group V sPLA(2) RNA was similarly modulated by DHA supplementation. In addition, DHA decreased Nox 4 expression and activity; this effect was associated with reduced production of reactive oxygen species. Further, the use of specific inhibitors allowed demonstrating that group V sPLA(2) is involved in the down-regulation of Nox 4 expression and activity by DHA. This interplay is mediated by ERK and PKC.

MeSH terms

  • Angiotensin II / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Antioxidants / pharmacology*
  • Calcimycin / pharmacology
  • Docosahexaenoic Acids / pharmacology*
  • Down-Regulation
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / enzymology
  • Humans
  • Interleukin-1beta / pharmacology
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • NADPH Oxidase 4
  • NADPH Oxidases / metabolism*
  • Phospholipases A2, Secretory / antagonists & inhibitors*
  • Phospholipases A2, Secretory / metabolism
  • Protein Kinase C / metabolism
  • Signal Transduction

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • Interleukin-1beta
  • Angiotensin II
  • Docosahexaenoic Acids
  • Calcimycin
  • NADPH Oxidase 4
  • NADPH Oxidases
  • NOX4 protein, human
  • Protein Kinase C
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Phospholipases A2, Secretory