# Unbiased assessment of 2-arachidonoylglycerol in cardiovascular inflammation

**Authors:** Moritz Nöthel, Franziska Dorer, Alexandru Odainic, Carolyn Krause, Marie Rüthing, Jasper Spitzer, Ulrike Strube, Theresia Weise, Dieter Lütjohann, Georg Nickenig, Susanne V. Schmidt, Julian Jehle

PMC · DOI: 10.1038/s41598-025-28969-5 · Scientific Reports · 2025-11-21

## TL;DR

This study shows that 2-AG promotes inflammation in heart conditions like myocardial infarction and left ventricular remodelling.

## Contribution

The study provides new evidence that 2-AG acts as a pro-inflammatory agent in cardiovascular inflammation.

## Key findings

- 2-AG induces a pro-inflammatory program in human monocytes, activating pathways like TNFα and IL-6.
- Higher levels of cardiac remodelling factors were observed in coronary arteries during acute coronary syndrome.
- Levels of remodelling factors correlate positively with 2-AG concentrations in patients.

## Abstract

2-arachidonoylglycerol (2-AG) is an endogenous modulator of inflammatory processes. Recent studies demonstrate its key role in inflammatory cardiovascular diseases, such as atherosclerosis and left ventricular remodelling. However, whether 2-AG acts as a pro- or anti-inflammatory agent in cardiovascular inflammation is a matter of controversial debate. CD14+ primary human monocytes were treated with 2-AG. Differentially expressed genes were determined by mRNA sequencing and used for bioinformatics analysis of changes in myeloid cell functions and cell signalling pathways. Additionally, we quantified cytokines and mediators involved in cardiac remodelling by multiplexing assays. Human monocytes responded to the treatment with 2-AG by inducing a pro-inflammatory cellular program. The top upregulated hallmark pathways were TNFα signalling via the NF-κB pathway, the inflammatory response and IL-6 signalling, illustrating the pro-inflammatory mode of action of 2-AG. These data were validated at the protein level in the supernatants of stimulated cells using multiplexing assays. Based on these in-vitro results, we examined blood samples from patients during acute and chronic coronary syndromes. By sampling blood from both the periphery and the culprit coronary artery, we observed a trend towards higher local concentrations of the cardiac remodelling factors Galectin-3, Osteopontin, and IP-10 in the coronary arteries of patients presenting with acute coronary syndrome compared with other groups. The levels of these remodelling factors correlate positively with 2-AG levels. Taken together, our data suggest that 2-AG acts as a pro-inflammatory agent in myocardial infarction and LV remodelling.

The online version contains supplementary material available at 10.1038/s41598-025-28969-5.

## Linked entities

- **Proteins:** LGALS3 (galectin 3), CXCL10 (C-X-C motif chemokine ligand 10), TNF (tumor necrosis factor), NFKB1 (nuclear factor kappa B subunit 1), IL6 (interleukin 6)
- **Chemicals:** 2-arachidonoylglycerol (PubChem CID 5282280), 2-AG (PubChem CID 5282280)
- **Diseases:** atherosclerosis (MONDO:0005311), myocardial infarction (MONDO:0005068), acute coronary syndrome (MONDO:0005542)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CD14 (CD14 molecule) [NCBI Gene 929], SPP1 (secreted phosphoprotein 1) [NCBI Gene 6696] {aka BNSP, BSPI, ETA-1, OPN}, LGALS3 (galectin 3) [NCBI Gene 3958] {aka CBP35, GAL3, GALBP, GALIG, L31, LGALS2}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** inflammatory cardiovascular diseases (MESH:D002318), cardiac remodelling (MESH:D020257), myocardial infarction (MESH:D009203), atherosclerosis (MESH:D050197), acute and chronic coronary syndromes (MESH:D054058), LV remodelling (MESH:D018487), cardiovascular inflammation (MESH:D007249)
- **Chemicals:** 2-AG (MESH:C094503)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12645022/full.md

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Source: https://tomesphere.com/paper/PMC12645022