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Title: Intestinal sucrase inhibitors and bile acid absorption in the rat

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5435738

Studies were carried out to determine if bile acid absorption is perturbed by the intestinal sucrase inhibitors, Acarbose and BAY m 1099 (1,5-dideoxy-1.5((2-hydroxy-ethyl) imino-)-D-glucitol). The intestinal absorption of taurocholic acid (TA) in male Wistar rats, anesthetized with pentobarbital (50mg/ig, i.p.), was assessed from its excretion rate in bile. In acute studies, 15 cm of distal ileum was perfused in vivo for 70 min with /sup 14/C-TA (0.1 mM, 5 ..mu.. Ci/mmol) in 0.154 M NaCl, 0.01 M phosphate (pH 6.8) and in some studies 20 mM sucrose. From 70-140 min the perfusate was unchanged or contained Acarbose (150, 1500 ..mu..g/ml) or BAY m 1099 (10, 25 ..mu..g/ ml). Neither drug without sucrose altered TA biliary excretion. With sucrose, BAY m 1099 (10 and 25 ..mu.. g/ml) reduced TA excretion by 11 and 22%; no greater effect occurred with 60..mu..g/ml. In subchronic studies rats were fed Acarbose (40 mg/100 g diet) or BAY m 1099 (10, 20, 40 mg/100 g diet) in AIN-76A (50% cornstarch, 15% sucrose) and after 8 wk /sup 14/C-TA (10 mg/kg, 0.08 ..mu..Ci/mg, 3 mg/ml 0.9% NaCl) was injected into the proximal small intestine. Neither drug affected the biliary excretion of TA, measured every 20 min for 4-5 hr. These studies indicate that neither acute nor subchronic regimes of Acarbose or BAY m 1099 affect the intestinal absorption of TA. A possible effect in the presence of sucrose is being explored.

Research Organization:
Boston Univ. School of Medicine, MA
OSTI ID:
5435738
Report Number(s):
CONF-8604222-; TRN: 86-026658
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 45:3; Conference: 70. annual meeting of the Federation of American Society for Experimental Biology, St. Louis, MO, USA, 13 Apr 1986
Country of Publication:
United States
Language:
English