Oral Fucoidan Attenuates Lung Pathology and Clinical Signs in a Severe Influenza a Mouse Model

Mar Drugs. 2020 May 8;18(5):246. doi: 10.3390/md18050246.

Abstract

Fucoidans are known to be effective inhibitors of inflammation, and of virus binding and cellular entry. Undaria pinnatifida-derived fucoidan (UPF) was assessed in a severe influenza A (H1N1, PR8) infection model in mice. Initially, UPF was gavaged at 3.52 mg daily in a treatment model. Gross lung pathology (consolidation) was significantly reduced as compared to controls. UPF was then presented as a feed supplement at a rate of either nil, 3.52 mg/day or 7.04 mg/day in a prophylactic model, dosed three days before infection. A significant improvement was observed in the clinical signs of ill-health, as well as a reduction in gross lung pathology in animals treated with the higher dose, although there was no significant reduction in lung viral titres.

Keywords: Undaria pinnatifida; anti-viral; fucoidan; inflammation; influenza; lung; mice.

MeSH terms

  • Administration, Oral
  • Animals
  • Dietary Supplements*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Humans
  • Influenza A Virus, H1N1 Subtype / isolation & purification
  • Influenza A Virus, H1N1 Subtype / pathogenicity
  • Influenza, Human / diagnosis
  • Influenza, Human / diet therapy*
  • Influenza, Human / pathology
  • Influenza, Human / virology
  • Lung / pathology
  • Lung / virology
  • Mice
  • Polysaccharides / administration & dosage*
  • Seaweed / chemistry*
  • Severity of Illness Index
  • Undaria / chemistry*
  • Viral Load

Substances

  • Polysaccharides
  • fucoidan