THE EFFECTS OF DIETARY SUPPLEMENTATION WITH YUCCA-SCHIDIGERA EXTRACT OR FRACTIONS THEREOF ON NITROGEN-METABOLISM AND GASTROINTESTINAL FERMENTATION PROCESSES IN THE RAT
Gf. Killeen et al., THE EFFECTS OF DIETARY SUPPLEMENTATION WITH YUCCA-SCHIDIGERA EXTRACT OR FRACTIONS THEREOF ON NITROGEN-METABOLISM AND GASTROINTESTINAL FERMENTATION PROCESSES IN THE RAT, Journal of the Science of Food and Agriculture, 76(1), 1998, pp. 91-99
Yucca schidigera was fractionated with butan-1-ol, yielding a butanol-
extractable (BE) fraction, containing all the in vitro antimicrobial a
ctivity, and the aqueous, non-butanol-extractable (NBE) fraction. Four
groups of five female rats (12 weeks old) were allowed ad libitum acc
ess to diets supplemented with water (control) or 200 mfi kg(-1) total
Y schidigera (TOT) or its fraction equivalent of NBE or BE for 64 day
s. The effects of the fractions and their interactions in the TOT trea
tment were analysed according to the factorial experimental structure
by two-way ANOVA. NBE reduced serum urea (-50%, P = 0.019) and ammonia
(-46%, P = 0.037) concentrations, serum/urine concentration quotients
of urea (-79%, P = 0.009) and ammonia (-57%, P = 0.002). NBE also red
uced hindgut acetate/propionate (-12%, P = 0.007) but increased faecal
ammonia concentration (+87%, P=0.039). BE reduced hindgut indoles (-2
5%, P = 0.023) and interacted synergystically with NBE in the TOT trea
tment to further reduce hindgut acetate/propionate by 6% (P = 0.006).
NBE increased (+27%, P = 0.002) and BE decreased (-57%, P = 0.005) hin
dgut urease activity levels, resulting in essentially no change (+ 4%)
in the TOT treatment. The in vitro antimicrobial activity of Y schidi
gera is an unlikely explanation for most of its effects in vivo becaus
e these are caused by NBE and in vitro antimicrobial activity is exclu
sive to BE. Sarsasapogenin and smilagenin were also exclusive (> 98%)
to BE and cannot account for the effects of Y schidigera on N metaboli
sm. (C) 1998 SCI.