TY - JOUR
T1 - Preserved organic anion transport in mutant TR- rats with a hepatobiliary secretion defect
AU - Jansen, P. L.
AU - van Klinken, J. W.
AU - van Gelder, M.
AU - Ottenhoff, R.
AU - Elferink, R. P.
PY - 1993
Y1 - 1993
N2 - The in vivo biliary secretion of a number of organic anions in mutant TR- rats was studied. The secretion of bilirubin glucuronide (BG), the glutathione conjugate of bromosulfophthalein, dibromosulfophthalein, and indocyanine green was reduced to 2, 15, 50, and 75% of normal, respectively. Surprisingly, the secretion of bilirubin ditaurate (BDT) was entirely normal under these conditions. In isolated TR- rat liver perfusion experiments (recirculating setup), the hepatobiliary secretion of BG and BDT was reduced to 1 and 50% of normal, respectively. There was considerable residual concentrative transport of BDT under these conditions (bile-to-perfusate concentration ratio of 190 +/- 60; normal, 730 +/- 480), whereas for BG the concentration step was completely abolished (bile-to-perfusate concentration ratio of 1.3 +/- 1.0; normal, 60 +/- 40). In a single-pass isolated TR- rat liver perfusion study, BDT secretion after bolus administration (1 mumol) was abnormal; the peak secretion was retarded to 20 min after injection (normal 7.5 min), and the secretion rate was decreased to 19% of normal. BDT, as an organic dianion, is a substrate for the "canalicular multispecific organic anion transporter" (cMOAT), a carrier protein that is defective in TR- rats. Its considerable residual secretion in certain experimental conditions suggests the preservation of a low-affinity pathway for secretion of some cMOAT substrates in TR- rats
AB - The in vivo biliary secretion of a number of organic anions in mutant TR- rats was studied. The secretion of bilirubin glucuronide (BG), the glutathione conjugate of bromosulfophthalein, dibromosulfophthalein, and indocyanine green was reduced to 2, 15, 50, and 75% of normal, respectively. Surprisingly, the secretion of bilirubin ditaurate (BDT) was entirely normal under these conditions. In isolated TR- rat liver perfusion experiments (recirculating setup), the hepatobiliary secretion of BG and BDT was reduced to 1 and 50% of normal, respectively. There was considerable residual concentrative transport of BDT under these conditions (bile-to-perfusate concentration ratio of 190 +/- 60; normal, 730 +/- 480), whereas for BG the concentration step was completely abolished (bile-to-perfusate concentration ratio of 1.3 +/- 1.0; normal, 60 +/- 40). In a single-pass isolated TR- rat liver perfusion study, BDT secretion after bolus administration (1 mumol) was abnormal; the peak secretion was retarded to 20 min after injection (normal 7.5 min), and the secretion rate was decreased to 19% of normal. BDT, as an organic dianion, is a substrate for the "canalicular multispecific organic anion transporter" (cMOAT), a carrier protein that is defective in TR- rats. Its considerable residual secretion in certain experimental conditions suggests the preservation of a low-affinity pathway for secretion of some cMOAT substrates in TR- rats
M3 - Article
C2 - 8214066
SN - 0002-9513
VL - 265
SP - G445-G452
JO - American Journal of Physiology
JF - American Journal of Physiology
IS - 3 Part 1
ER -