Limosilactobacillus reuteri HY7503 and Its Cellular Proteins Alleviate Endothelial Dysfunction by Increasing Nitric Oxide Production and Regulating Cell Adhesion Molecule Levels

Int J Mol Sci. 2024 Oct 21;25(20):11326. doi: 10.3390/ijms252011326.

Abstract

Endothelial dysfunction, which is marked by a reduction in nitric oxide (NO) production or an imbalance in relaxing and contracting factor levels, exacerbates atherosclerosis by promoting the production of cell adhesion molecules and cytokines. This study aimed to investigate the effects of Limosilactobacillus reuteri HY7503, a novel probiotic isolated from raw milk, on endothelial dysfunction. Five lactic acid bacterial strains were screened for their antioxidant, anti-inflammatory, and endothelium-protective properties; L. reuteri HY7503 had the most potent effect. In a mouse model of angiotensin II-induced endothelial dysfunction, L. reuteri HY7503 reduced vascular thickening (19.78%), increased serum NO levels (226.70%), upregulated endothelial NO synthase (eNOS) expression in the aortic tissue, and decreased levels of cell adhesion molecules (intercellular adhesion molecule-1 [ICAM-1] and vascular cell adhesion molecule-1 [VCAM-1]) and serum cytokines (tumor necrosis factor-alpha [TNF-α] and interleukin-6 [IL-6]). In TNF-α-treated human umbilical vein endothelial cells (HUVECs), L. reuteri HY7503 enhanced NO production and reduced cell adhesion molecule levels. In HUVECs, surface-layer proteins (SLPs) were more effective than extracellular vesicles (exosomes) in increasing NO production and decreasing cell adhesion molecule levels. These findings suggested that L. reuteri HY7503 may serve as a functional probiotic that alleviates endothelial dysfunction.

Keywords: Limisilactobacillus reuteri; angiotensin II; endothelial dysfunction; lactic acid bacteria; probiotics.

MeSH terms

  • Animals
  • Cell Adhesion Molecules / metabolism
  • Cytokines / metabolism
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / microbiology
  • Human Umbilical Vein Endothelial Cells* / metabolism
  • Humans
  • Limosilactobacillus reuteri* / metabolism
  • Male
  • Mice
  • Nitric Oxide* / metabolism
  • Probiotics*
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Nitric Oxide
  • Cell Adhesion Molecules
  • Cytokines
  • Vascular Cell Adhesion Molecule-1

Grants and funding

This study received no external funding.