Inhibitory effect of exendin-4 on secretory group IIA phospholipase A2

Biochem Biophys Res Commun. 2015 Apr 17;459(4):650-4. doi: 10.1016/j.bbrc.2015.02.165. Epub 2015 Mar 7.

Abstract

Exendin-4 (EX4), a glucagon-like peptide-1 receptor agonist, has been reported to attenuate myocardial ischemia and reperfusion injury and inflammatory or oxidative responses. The expression level of secretory group IIA phospholipase A2 (sPLA2-IIA) is elevated in inflammatory diseases. Lipopolysaccharide (LPS) upregulates the expression of sPLA2-IIA in human umbilical vein endothelial cells (HUVECs). Here, EX4 was examined for its effects on the expression and activity of sPLA2-IIA in HUVECs and mice. Pre-treatment of cells or mice with EX4 inhibited LPS-induced sPLA2-IIA expression and activity. Additionally, EX4 suppressed LPS-induced activation of cytosolic phospholipase A2 (cPLA2) and extracellular signal-regulated kinase (ERK) 1/2. Therefore, these results show that EX4 inhibited LPS-induced expression of sPLA2-IIA by suppressing cPLA2 and ERK 1/2.

Keywords: Exendin-4; HUVEC; Inflammation; sPLA2-IIA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Exenatide
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Peptides / physiology*
  • Phospholipases A2
  • Venoms

Substances

  • Peptides
  • Venoms
  • Exenatide
  • Phospholipases A2