Jc. Meslin et al., EFFECTS OF GALACTO-OLIGOSACCHARIDE AND BACTERIAL STATUS ON MUCIN DISTRIBUTION IN MUCOSA AND ON LARGE-INTESTINE FERMENTATION IN RATS, British Journal of Nutrition, 69(3), 1993, pp. 903-912
The purpose of the present paper was to study the effects of a dietary
undigestible carbohydrate and intestinal microflora on mucin distribu
tion (neutral, acid, sulphonated), glycolytic activities: beta-D-galac
tosidase (EC 3.2.1.23), N-acetyl-beta-D-galactosaminidase (EC 3.2.1.43
), N-acetyl-beta-D-glucosaminidase (EC 3.2.1.30), alpha-L-fucosidase (
EC 3.2.1.51) and bacterial metabolism (gas production, short-chain fat
ty acids (SCFA) and lactic acid caecal concentration) in germ-free (GF
), conventional (CV) and heteroxenic (HE) rats (GF rats associated wit
h a human flora). Rats were fed on either a control diet or a diet con
taining 40 g trans-galactosylated oligosaccharide (TOS)/kg. In GF rats
fed on the control diet caecal pH was almost neutral and glycolytic a
ctivities negligible. The number of mucus-containing cells increased f
rom the caecum to the colon for the three types of mucin. TOS had no e
ffect in the caecum but it modified mucin cell repartition in the colo
n. In CV and HE rats fed on the control diet caecal pH was similar (6.
8), but caecal SCFA and lactic acid concentrations (mumol/g) and gas p
roduction (ml/24 h) were higher in CV (70, 5.9 and 2-3 respectively) t
han in HE rats (32, 4.6 and 0.4 respectively). In CV, as in HE rats, a
cid-mucin-containing cells increased from the caecum to the colon and
glycolytic activities were similar. TOS reduced acid-mucin-containing
cells in the caecum of CV rats by twofold but had no effect in either
the caecum or the colon of HE rats. TOS strongly beta-increased galact
osidase activity and slightly modified the other glycolytic activities
. Its effect on bacterial metabolites depended on bacterial status. Ho
wever, comparison between CV and HE rats showed no evident relationshi
p between the number of mucus-containing cells and measured bacterial
metabolites. Differences between CV and HE rats might be due to bacter
ial microflora specificity. TOS had an intrinsic effect on mucus cell
distribution in the colon of GF rats. In CV and HE rats the presence o
f the flora abolished this effect.