Abstract
A polysaccharide ( M w 2.39 × 10 4 g/mol) was extracted with cold water from the basidiomycete Pleurotus pulmonarius, and its antinociceptive and anti-inflammatory properties were evaluated. It was a mannogalactan (MG), whose structure was characterized using mono- and two-dimensional NMR spectroscopy, methylation analysis, and a controlled Smith degradation. It had a main chain of (1 → 6)-linked α- d-galactopyranosyl and 3- O-methyl-α- d-galactopyranosyl units, both of which are partially substituted at O-2 by β- d-mannopyranosyl non-reducing ends. The MG was tested for its effects on the acetic acid-induced writhing reaction in mice, a typical model for inflammatory pain, causing a marked and dose-dependent inhibition of the nociceptive response, with ID 50 of 16.2 (14.7–17.7) mg/kg and inhibition of 93 ± 3% at a dose of 30 mg/kg. An inflammatory response was not inhibited.
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