P. Valette et al., BIOAVAILABILITY OF NEW SYNTHESIZED GLUCOOLIGOSACCHARIDES IN THE INTESTINAL-TRACT OF GNOTOBIOTIC-RATS, Journal of the Science of Food and Agriculture, 62(2), 1993, pp. 121-127
Using germ-free rats and previously germ-free rats inoculated with a c
omplex human flora (heteroxenic rats), the digestibility of new glucoo
ligosaccharides (GOS) and the effect of the digestive flora on their f
ermentation were studied. The GOS were synthesized using a glucosyltra
nsferase reaction and were composed of a mixture of mono- to heptasacc
harides (degree of polymerisation (DP) from 1 to 7), with alpha-1,6 an
d alpha-1,2 linkages. In germ-free rats, two diets containing GOS (20
g kg-1 diet and 40 g kg-1 diet) were compared to a control diet contai
ning sucrose. The extent of GOS digestion was about 20 % and the major
component, DP 5, was almost fully resistant to the action of endogeno
us enzymes. In heteroxenic rats, only GOS (20 g kg-1 diet) was compare
d to the control diet. Gaseous H-2 and CH4 excretions measured in a re
spiratory chamber significantly increased by GOS fermentation (1.8 and
2.9 times, respectively, P < 0.001). As compared to the control group
, there were no modifications of the pH, short-chain fatty acids (SCFA
), and lactic acid concentrations in the caecum of rats fed with the G
OS diet, but there were changes of the SCFA profile, ie butyric, isobu
tyric and isovaleric acid proportions significantly decreased (P < 0.0
1), whereas the caproic acid proportion increased (P < 0.05). GOS appe
ared to be completely fermented. Changes in the gaseous excretion and
in the SCFA profile suggest that the intake of a low amount of this ne
w synthetised GOS led to some decrease in the proteolytic activity and
in an enhancement of the glycolytic fermentation.