Isolated, vascularly perfused, rat duodenojejunum and ileum preparatio
ns were used to study the transport parameters of cholyltaurine (C-tau
; taurocholate). After a bolus administration of C-tau containing trac
e amounts of [H-3]C-tau into the lumen of the isolated vascularly perf
used duodenojejunum, the rate of appearance of C-tau in the portal eff
luent was dose-dependent over the range 5-20 mM. At a concentration of
20 mM, the rate of absorption was constant over time and amounted to
1.25 nmol . ml(-1). cm(-1); 2.6% of the luminal load of C-tau was reco
vered in the portal effluent over the 40-min experimental period. Intr
a-arterial infusion of ouabain (10(-3) M) did not modify significantly
the absorption rate of C-tau. The C-tau absorption from the lumen of
the isolated vascularly perfused ileum was 7-fold higher than that fro
m the duodenojejunum. Total absorption of C-tau was dose-dependent ove
r the range 1-20 mM and the estimated K-m and T-max of the absorptive
area of the rat ileum were 11.5 mM and 17.7 nmol . min(-1). cm(-1), re
spectively. Intraarterial infusion of ouabain reduced by 84% the recov
ery of C-tau in the portal effluent. In conclusion, the absorption par
ameters of bile acids in the duodenojejunum and in the ileum of the ex
vivo rat intestinal preparations are consistent with a passive diffus
ion process in the proximal small intestine and an active transport in
the ileum. The isolated vascularly perfused duodenojejunum and ileum
preparations are therefore appropriate models for studying bile acid a
bsorption process and the coupling with the associated local metabolic
, motor, secretory and vascular events.