Mo3Se4 nanoparticle with ROS scavenging and multi-enzyme activity for the treatment of DSS-induced colitis in mice

Redox Biol. 2022 Oct:56:102441. doi: 10.1016/j.redox.2022.102441. Epub 2022 Aug 14.

Abstract

Ulcerative colitis (UC), as a most common inflammatory bowel disease (IBD), has become a global public health concern. Exploring novel method of treating UC is urgent and necessary. Recently, nanozyme with excellent antioxidant properties may be one useful therapeutic strategy. In this study, a two-dimensional transition metal chalcogenide (TMCs) nano flake and polyethylene glycol (PEG) modified Mo3Se4 nano flakes (PMNFs) was synthesized, which had multi-enzyme activity, including peroxidase, glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT). The inhibition effect of PMNFs on sodium dextran sulfate (DSS)-induced colitis was explored. UC was effectively inhibited by PMNFs in this work. PMNFs significantly reduced disease activity index (DAI) score, including weight loss, colon shorten and histopathological abnormalities. The possible mechanism of PMNFs-attenuated colitis was investigated. The results showed that PMNFs reversed DSS-induced oxidative damage, and the antioxidant pathway Nrf2-keap1 signal was activated by PMNFs. Moreover, PMNFs suppressed the expression of pro-inflammatory factors including IL-1β, TNF-α, IFN-β and IL-6 via the inactivation of TLR4/NF-κB pathway in DSS-induced colitis and LPS-treated macrophage. Furthermore, PMNFs treatment prevented the reduction of tight junction proteins (ZO-1, occludin, and claudin-1) and mucin-2 (MUC-2) as well as the up-regulation of epithelial apoptosis caused by DSS. These findings demonstrate that the PMNFs against DSS-induced colitis due to its prevention on oxidative damage, inflammation, and intestine barrier breakdown. Thus, PMNFs have a potential application in the treatment of various oxidative stress or inflammation-related diseases.

Keywords: Inflammation; Intestinal barrier; Mo(3)Se(4) nanozyme; Oxidative stress; Ulcerative colitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Antioxidants / therapeutic use
  • Catalase / metabolism
  • Claudin-1 / metabolism
  • Claudin-1 / therapeutic use
  • Colitis* / chemically induced
  • Colitis* / drug therapy
  • Colitis* / metabolism
  • Dextran Sulfate / adverse effects
  • Disease Models, Animal
  • Glutathione Peroxidase / metabolism
  • Inflammation
  • Interleukin-6 / metabolism
  • Kelch-Like ECH-Associated Protein 1 / metabolism
  • Lipopolysaccharides / adverse effects
  • Mice
  • Mice, Inbred C57BL
  • Mucin-2 / metabolism
  • NF-E2-Related Factor 2 / metabolism
  • NF-kappa B / metabolism
  • Nanoparticles*
  • Occludin / metabolism
  • Polyethylene Glycols
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase / metabolism
  • Tight Junction Proteins / metabolism
  • Toll-Like Receptor 4 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antioxidants
  • Claudin-1
  • Interleukin-6
  • Kelch-Like ECH-Associated Protein 1
  • Lipopolysaccharides
  • Mucin-2
  • NF-E2-Related Factor 2
  • NF-kappa B
  • Occludin
  • Reactive Oxygen Species
  • Tight Junction Proteins
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Polyethylene Glycols
  • Dextran Sulfate
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase