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

Biochem Biophys Res Commun · 2015

Last updated 2026-05-28

A study tested exendin-4 (EX4), a GLP-1 drug, on cells and mice to see if it could reduce inflammation. EX4 reduced the activity of a protein called sPLA2-IIA, which increases during inflammation, by blocking two other proteins involved in this process.

AI summary of the abstract below.

JournalBiochem Biophys Res Commun, 2015
Citations3
Relative citation ratio0.13
NIH percentile9
Molecules

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.

Verbatim abstract via PubMed 25757907 ↗