Inhibitory effect of exendin-4 on secretory group IIA phospholipase A2.
Biochem Biophys Res Commun · 2015
Last updated 2026-05-28A 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.
| Journal | Biochem Biophys Res Commun, 2015 |
|---|---|
| Citations | 3 |
| Relative citation ratio | 0.13 |
| NIH percentile | 9 |
| 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 ↗