Background--Mucins play an important protective role in the colonic mucosa.
Luminal factors modulating colonic mucus release have been not fully ident
ified.
Aim--To determine the effect of some dietary compounds on mucus discharge i
n rat colon.
Methods-An isolated vascularly perfused rat colon model was used. Mucus sec
retion was induced by a variety of luminal factors administered as a bolus
of 1 mi for 30 minutes in the colonic loop. Mucin release was evaluated usi
ng a sandwich enzyme linked immunosorbent assay supported by histological a
nalysis.
Results--The three dietary fibres tested in this study (pectin, gum arabic,
and cellulose) did not provoke mucus secretion. Luminal administration of
sodium alginate (an algal polysaccharide used as a food additive) or ulvan
(a sulphated algal polymer) induced a dose dependent increase in mucin disc
harge over the concentration range 1-25 mg/l (p<0.05 for 25 mg/l alginate a
nd p<0.05 for 10 and 25 mg/l ulvan). Glucuronic acid and galacturonic acid,
which are major constituents of a variety of fibres, produced significant
mucin secretion (p<0.05). Hydrogen sulphide and mercaptoacetate, two sulphi
des produced in the colonic lumen by microbial fermentation of sulphated po
lysaccharides, did not modify mucin secretion. Among the short chain fatty
acids, acetate (5-100 mM) induced a dose dependent release of mucus (p<0.05
for 100 mM acetate). Interestingly, butyrate at a concentration of 5 mM pr
oduced colonic mucin secretion (p<0.05), but increasing its concentration t
o 100 mM provoked a gradual decrease in mucus discharge. Propionate (5-100
mM) did not induce mucin release. Several dietary phenolic compounds (querc
etin, epicatechin, resveratrol) did not provoke mucus discharge.
Conclusions--Two algal polysaccharides (alginate and ulvan), two uronic aci
ds (glucuronic acid and galacturonic acid), and the short chain fatty acids
acetate and butyrate induce mucin secretion in rat colon. Taken together,
these data suggest that some food constituents and their fermentation produ
cts may regulate the secretory function of colonic goblet cells.