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  • Betula pendula  (1)
  • ruminant  (1)
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  • 1
    ISSN: 1573-1561
    Keywords: Phenol ; platyphylloside ; digestibility ; plant defense ; ruminant ; birch
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Extracts of Scandinavian birch (Betula pendula Roth) buds and internodes of varying twig diameters have been investigated for their inhibitory effect on ruminant digestibility in vitro. The predominant inhibitory effect was observed in extracts containing the phenol platyphylloside, 5-hydroxy-1,7-bis-(4-hydroxy-phenyl)-3-heptan-one-3-O-β-d-glucopyranoside. Isolation of the pure compound and incubation with rumen inocula showed that digestibility was negatively related to the concentration. Significant effect was measured below the concentration naturally occurring in birch (0.8% of dry matter). Another isolated compound, the closely related rhododendrin, 4-(4-hydroxyphenyl)-2-butanol-2-O-β-d-glucopyranoside, did not depress digestibility within the concentrations found in birch. An important phenol of buds, apigenin-4′,7-dimethylether, did not have any measurable effect on digestibility, while a nonphenolic fraction of bud extract had a slight inhibitory effect on digestibility. Implications for browsers feeding on birch are briefly discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 25 (1999), S. 2703-2713 
    ISSN: 1573-1561
    Keywords: Platyphylloside ; 5-hydroxy-3-platyphyllone ; centrolobol ; phenols ; rumen fluid ; birch bark ; Betula pendula
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract (±)-5-Hydroxy-1,7-bis-(4′-hydroxyphenyl)-3-heptanone (2a), (±)-5-hydroxyl-1-(4′-hydroxyphenyl)-7-phenyl-3-heptanone (2b), (±)-5-hydroxy-7-(4′-hydroxyphenyl)-1-phenyl-3-heptanone (2c), and (±)-5-hydroxy-1,7-bis-(phenyl)-3-heptanone (2d) have been synthesized to study the structure–activity relationship regarding digestibility inhibition in vitro in cow rumen fluid. The activities were compared with the activity of chiral (S)-2a and its glucoside platyphylloside (1), isolated from Betula pendula. Compound 2a was slightly less active, 2b and 2c were more active, and 2d was less active than (S)-2a and platyphylloside.
    Type of Medium: Electronic Resource
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