# Anti-Atherogenic Activities of Exopolysaccharides and Their Producing Strain Limosilactobacillus fermentum MC1 in Mice

**Authors:** Nada Oršolić, Barbara Toljanić, Dyana Odeh, Nina Čuljak, Kate Šešelja, Mirela Baus Lončar, Domagoj Đikić, Andreja Leboš Pavunc, Blaženka Kos

PMC · DOI: 10.3390/ijms27052473 · 2026-03-07

## TL;DR

This study explores how a probiotic strain and its exopolysaccharides may reduce atherosclerosis and cardiovascular disease in mice through anti-inflammatory and antioxidant effects.

## Contribution

The novel contribution is demonstrating the anti-atherogenic potential of Limosilactobacillus fermentum MC1 and its exopolysaccharides in a mouse model.

## Key findings

- L. fermentum MC1 and its EPSs reduced lipid and atherogenic parameters in mice.
- The treatment showed antioxidant, anti-inflammatory, and immunomodulatory effects in the gut and systemic tissues.
- EPSs and the strain improved lipid metabolism and reduced oxidative stress markers.

## Abstract

Atherosclerosis, the leading cause of death worldwide, is a chronic inflammatory disease leading to the accumulation of lipid-rich plaques within the artery wall. Accumulating evidence indicates that intestinal microbiota plays an important regulatory role in atherosclerosis at all stages of the disease. Through numerous metabolites, the intestinal microbiota can regulate immune and inflammatory cells and their mediators, as well as lipid metabolism, thereby contributing to the development and progression of atherosclerosis. With these assumptions in mind, we investigated the possibility of using Limosilactobacillus fermentum MC1 (L. fermentum MC1) and its exopolysaccharides (EPSs) in the reduction of lipid and atherogenic parameters as a preventive strategy in preventing the occurrence of cardiovascular diseases (CVD). We investigated the effect of L. fermentum MC1 and its EPSs on the health status of mice by monitoring the following parameters: body weight, colon length and weight, relative weight of organs, hematological (Hgb, WBC, number of erythrocytes, MCHC, MCV, MCH), and biochemical blood parameters including glucose, serum enzymes (ALT, ALP, amylase), urea, creatinine and lipid profile (total cholesterol, triglycerides, HDL, VLDL, LDL), different atherogenic parameters, blood biomarkers such as lymphocyte-to-monocyte (LMR) and neutrophil-to-lymphocyte (NLR) ratios, molecular inflammatory markers (IL1β, IL6, MCP1, IL1α, TLR4, TNFα, CD68, TGFβ), apoptosis markers (BCL2, AIFM1, IGF-1R), and endoplasmic reticulum stress markers (CHOP and GRP94) as well as oxidative stress (NOX2) markers in the colon. Furthermore, the level of lipid peroxidation, nitric oxide and glutathione concentrations in the liver, kidneys and spleen were measured. L. fermentum MC1 and its EPSs may prevent the development of atherosclerosis and the progression of CVD through antioxidant, anti-inflammatory, immunomodulatory activities, and regulation of the gut microbiome and lipid metabolism. The observed reduction in lipid and atherogenic determinants suggests that L. fermentum MC1 and its EPSs may contribute to atheroprotection and confer multiple health benefits.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), CCL2 (C-C motif chemokine ligand 2), IL1A (interleukin 1 alpha), TLR4 (toll like receptor 4), TNF (tumor necrosis factor), CD68 (CD68 molecule), TGFB1 (transforming growth factor beta 1), BCL2 (BCL2 apoptosis regulator), AIFM1 (apoptosis inducing factor mitochondria associated 1), IGF1R (insulin like growth factor 1 receptor), DDIT3 (DNA damage inducible transcript 3), HSP90B1 (heat shock protein 90 beta family member 1), CYBB (cytochrome b-245 beta chain)
- **Diseases:** atherosclerosis (MONDO:0005311)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), Atherogenic (MESH:D050197), CVD (MESH:D002318), death (MESH:D003643)
- **Chemicals:** glucose (MESH:D005947), urea (MESH:D014508), glutathione (MESH:D005978), creatinine (MESH:D003404), lipid (MESH:D008055), triglycerides (MESH:D014280), EPSs (-), cholesterol (MESH:D002784), nitric oxide (MESH:D009569)
- **Species:** gut metagenome (species) [taxon 749906], Mus musculus (house mouse, species) [taxon 10090]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985991/full.md

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Source: https://tomesphere.com/paper/PMC12985991