Structural Characterization and In Vivo Anti-Inflammatory Activity of Fucoidan from Cystoseira crinita (Desf.) Borry

Mar Drugs. 2022 Nov 15;20(11):714. doi: 10.3390/md20110714.

Abstract

The aim of this study was to evaluate the effects of fucoidan isolated from C. crinita on histamine-induced paw inflammation in rats, and on the serum levels of TNF-α, IL-1β, IL-6, and IL-10 in rats during systemic inflammation response. The levels of TNF-α in a model of acute peritonitis in rats were also investigated. The isolated crude fucoidan was identified as a sulfated xylogalactofucan with high, medium, and low molecular weight fractions and a content of fucose of 39.74%, xylose of 20.75%, and galactose of 15.51%. Fucoidan from C. crinita showed better anti-inflammatory effects in the rat paw edema model, and this effect was present during all stages of the experiment. When compared to controls, a commercial fucoidan from F. vesiculosus, the results also displayed anti-inflammatory activity on the 60th, 90th, and 120th minute of the experiment. A significant decrease in serum levels of IL-1β in rats treated with both doses of C. crinita fucoidan was observed in comparison to controls, whereas TNF-α concentrations were reduced only in the group treated with fucoidan from C. crinita at the dose of 25 mg/kg bw. In the model of carrageenan-induced peritonitis, we observed a tendency of decrease in the levels of the pro-inflammatory cytokine TNF-α in peritoneal fluid after a single dose of C. crinita fucoidan, but this did not reach the statistical significance margin. Single doses of C. crinita fucoidan did not alter serum levels of the anti-inflammatory cytokine IL-10 in animals with lipopolysaccharide-induced systemic inflammation.

Keywords: Cystoseira crinita; IL-1β; TNF-α; anti-inflammatory effect; cytokines; fucoidan; peritonitis; rat paw edema.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents* / pharmacology
  • Cytokines
  • Inflammation* / chemically induced
  • Inflammation* / drug therapy
  • Interleukin-10
  • Peritonitis* / chemically induced
  • Peritonitis* / drug therapy
  • Phaeophyceae* / chemistry
  • Rats
  • Tumor Necrosis Factor-alpha

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • fucoidan
  • Interleukin-10
  • Tumor Necrosis Factor-alpha

Grants and funding

This research was funded by Medical University–Plovdiv through the Doctoral and Postdoctoral project-02/2019. The APC was funded by the same institution.