TY - JOUR
T1 - Effect of colestimide on absorption of unconjugated bile acids in the rat jejunum
AU - Onishi, Toshiki
AU - Sano, Naoyo
AU - Takikawa, Hajime
PY - 2002
Y1 - 2002
N2 - Background: Colestimide is a newly developed bile acid-binding resin in Japan, but its bile acid-binding properties have not been studied. Methods: The absorption of unconjugated bile acids (5 mmol/L) in the ligated rat jejunum was compared in the presence and absence of colestimide. Furthermore, bile acid adsorption by colestimide was also studied in vitro. Results: All bile acids were efficiently absorbed in the jejunum and the cumulative absorption during 120 min was 29-63%. The absorption of chenodeoxycholate, lithocholate, deoxycholate and ursodeoxycholate was dose-dependently inhibited by 2.5 and 5 mg colestimide, whereas the absorption of cholate was not inhibited, even in the presence of 5 mg colestimide. Adsorption of bile acids by colestimide in vitro was approximately 60% for chenodeoxycholate, lithocholate, deoxycholate and ursodeoxycholate, whereas the adsorption of cholate was low (16%). Conclusions: Jejunal absorption of ursodeoxycholate was inhibited by colestimide to a similar extent as other dihydroxy bile acids, whereas that of cholate was not inhibited under the same conditions.
AB - Background: Colestimide is a newly developed bile acid-binding resin in Japan, but its bile acid-binding properties have not been studied. Methods: The absorption of unconjugated bile acids (5 mmol/L) in the ligated rat jejunum was compared in the presence and absence of colestimide. Furthermore, bile acid adsorption by colestimide was also studied in vitro. Results: All bile acids were efficiently absorbed in the jejunum and the cumulative absorption during 120 min was 29-63%. The absorption of chenodeoxycholate, lithocholate, deoxycholate and ursodeoxycholate was dose-dependently inhibited by 2.5 and 5 mg colestimide, whereas the absorption of cholate was not inhibited, even in the presence of 5 mg colestimide. Adsorption of bile acids by colestimide in vitro was approximately 60% for chenodeoxycholate, lithocholate, deoxycholate and ursodeoxycholate, whereas the adsorption of cholate was low (16%). Conclusions: Jejunal absorption of ursodeoxycholate was inhibited by colestimide to a similar extent as other dihydroxy bile acids, whereas that of cholate was not inhibited under the same conditions.
KW - Anion-exchange resin
KW - Bile acids
KW - Colestimide
KW - Intestinal absorption
KW - Ursodeoxycholic acid
UR - https://www.scopus.com/pages/publications/0036019528
U2 - 10.1046/j.1440-1746.2002.02765.x
DO - 10.1046/j.1440-1746.2002.02765.x
M3 - 記事
C2 - 12100616
AN - SCOPUS:0036019528
SN - 0815-9319
VL - 17
SP - 697
EP - 701
JO - Journal of Gastroenterology and Hepatology (Australia)
JF - Journal of Gastroenterology and Hepatology (Australia)
IS - 6
ER -