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Center for Basic Research in Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Medical School, Clinic, and Foundation, Rochester, Minnesota 55905
The physiological relevance of the
absorption of glucose from bile by cholangiocytes remains unclear. The
aim of this study was to test the hypothesis that absorbed glucose
drives aquaporin (AQP)-mediated water transport by biliary epithelia
and is thus involved in ductal bile formation. Glucose absorption and
water transport by biliary epithelia were studied in vitro by
microperfusing intrahepatic bile duct units (IBDUs) isolated from rat
liver. In a separate set of in vivo experiments, bile flow and
absorption of biliary glucose were measured after intraportal infusion
of D-glucose or phlorizin. IBDUs absorbed
D-glucose in a dose- and phlorizin-dependent manner with an
absorption maximum of 92.8 ± 6.2 pmol · min
1 · mm
1.
Absorption of D-glucose by microperfused IBDUs resulted in
an increase of water absorption (Jv = 3
10
nl · min
1 · mm
1,
Pf = 40 × 10
3 cm/sec).
Glucose-driven water absorption by IBDUs was inhibited by
HgCl2, suggesting that water passively follows
absorbed D-glucose mainly transcellularly via
mercury-sensitive AQPs. In vivo studies showed that as the amount of
absorbed biliary glucose increased after intraportal infusion of
D-glucose, bile flow decreased. In contrast, as the
absorption of biliary glucose decreased after phlorizin, bile flow
increased. Results support the hypothesis that the physiological
significance of the absorption of biliary glucose by cholangiocytes is
likely related to regulation of ductal bile formation.
liver; cholangiocytes; absorption; secretion; aquaporins; phlorizin; microperfusion; intrahepatic bile duct units
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