The aim of this study was to examine whether tauroursodeoxy-cholate (TUDC)
and cholestyramine resin (CR) enhance biliary carcinogenesis in the hamster
model, A cholecystoduodenostomy with dissection of the extrahepatic bile d
uct on the distal end of the common duct was performed on Syrian hamsters.
The hamsters were then divided randomly into 3 groups: control group, TUDC-
treated group, and CR-treated group. All animals received N-nitrosobis(2-ox
opropyl)amine (BOP) to initiate pancreaticobiliary cancer. The experiment w
as terminated at week 16 and the number of neoplastic lesions was counted m
icroscopically. In the TUDC group, the intrahepatic biliary carcinogenesis
was more accelerated than that observed in the control group, but no promot
ing effect was seen in the pancreas, gallbladder, or extrahepatic bile duct
, In the CR group, both the intrahepatic biliary and the gallbladder carcin
ogenesis were inhibited compared with that observed in the control group an
d the TUDC group. TUDC enhanced the intrahepatic bile duct carcinogenesis,
whereas CR inhibited both the intrahepatic bile duct and the gallbladder ca
rcinoma. Bile acids were suggested to promote biliary carcinoma in the hams
ter model.