Structural characteristics and biological effects of exopolysaccharide produced by cyanobacterium Nostoc sp
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
32442574
DOI
10.1016/j.ijbiomac.2020.05.135
PII: S0141-8130(20)33288-8
Knihovny.cz E-resources
- Keywords
- Biological activities, Cyanobacteria, Extracellular polysaccharide,
- MeSH
- Albuterol pharmacology MeSH
- Polysaccharides, Bacterial chemistry pharmacology MeSH
- Biopolymers chemistry MeSH
- Bronchodilator Agents pharmacology MeSH
- Cell Line MeSH
- Cytokines metabolism MeSH
- Interleukin-6 metabolism MeSH
- Cough drug therapy MeSH
- Codeine pharmacology MeSH
- Glucuronic Acid chemistry MeSH
- Uronic Acids chemistry MeSH
- Macrophages drug effects metabolism MeSH
- Guinea Pigs MeSH
- Mice MeSH
- Nostoc metabolism MeSH
- Nitric Oxide metabolism MeSH
- RAW 264.7 Cells MeSH
- Cyanobacteria metabolism MeSH
- Tumor Necrosis Factor-alpha metabolism MeSH
- Animals MeSH
- Check Tag
- Guinea Pigs MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Albuterol MeSH
- Polysaccharides, Bacterial MeSH
- Biopolymers MeSH
- Bronchodilator Agents MeSH
- Cytokines MeSH
- Interleukin-6 MeSH
- Codeine MeSH
- Glucuronic Acid MeSH
- Uronic Acids MeSH
- Nitric Oxide MeSH
- Tumor Necrosis Factor-alpha MeSH
Complex structure of cyanobacterium Nostoc sp. exopolysaccharide (EPS), with apparent molecular weight 214 × 103 g/mol, can be deduced from its composition. Chemical and NMR analyses found four dominant sugar monomers, namely (1 → 4)-linked α-l-arabinopyranose, β-d-glucopyranose, β-d-xylopyranose and (1 → 3)-linked β-d-mannopyranose, two different uronic acids and a lactyl group, with (1 → 4,6)-linked β-d-glucopyranose as the only branch point suggest a complex structure of this polymer. The dominant uronic acid is α-linked, but it remained unidentified. β-d-Glucuronic acid was present in lower amount. Their position as well as that of lactyl remained undetermined too. Different doses of orally administered EPS in guinea pigs evoked a significant decrease in cough effort and a decrease in airway reactivity. The antitussive efficacy and bronchodilator effect of higher doses of EPS were found to be similar to that of the antitussive drug codeine and the antiasthmatic salbutamol. Without significant cytotoxicity on the RAW 264.7 cells, EPS stimulated the macrophage cells to produce pro-inflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), and prostaglandins (PGs) and nitric oxide (NO) via induction of COX-2 and iNOS expression, respectively, suggesting that this biopolymer potentiates an early innate immune response and can therefore be used as a new immune modulator.
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