R. Aldini et al., HEPATIC-UPTAKE AND INTESTINAL-ABSORPTION OF BILE-ACIDS IN THE RABBIT, European journal of clinical investigation, 24(10), 1994, pp. 691-697
The existence of transporters for bile acids (BA) in liver and intesti
ne has been well documented, but information is still needed as to the
ir respective transport capacity. In the present investigation, we com
pared the hepatic and intestinal transport rates for BA, using perfuse
d livers and intestines. The livers and intestines were separately per
fused and dose-response curves (0.25-10 mM) for tauroursodeoxycholate,
taurocholate and taurodeoxycholate were obtained. The intestinal and
mesenteric concentration and bile acid pattern were also evaluated in
six non-fasting rabbits. Taurocholic, tauroursodeoxycholic and taurode
oxycholic acid ileal absorption showed saturation kinetics in the inte
stine as in the liver; the maximal uptake velocity for each bile acid
in the liver was tenfold higher than the respective maximal transport
velocity in the intestine; the Km values obtained in the liver were of
the same order of magnitude, i.e. in the millimolar range. Taurocholi
c, tauroursodeoxycholic and taurodeoxycholic acid transport difference
s in the liver paralleled those in the intestine. Although the intesti
ne was not homegeneously filled, the bile acid concentration in the il
eal content fell into the range of the Km for the three studied bile a
cids, while the portal blood total bile acid concentration was inferio
r to the observed Kms of liver uptake. Therefore, both the hepatic and
intestinal systems do not operate at their maximal transport rates at
the prevailing concentrations in portal blood and luminal content, an
d the hepatic transport occurs at its highest efficiency (below the Km
values) in physiological conditions.