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Journal of Lipid Research, Vol 31, 1015-1021, Copyright © 1990 by Lipid Research, Inc.
M Une, K Yamanaga, EH Mosbach, K Tsujimura and T Hoshita
The metabolism of 7-ethyl- and 7-propyl-chenodeoxycholic acids was studied
in hamsters. Both bile acid analogs were absorbed efficiently by the
intestine and secreted into the bile at rates similar to those of
chenodeoxycholic acid. After intraduodenal administration into bile fistula
hamsters, the 7-alkyl analogs were present in bile as the glycine and
taurine conjugates. The glycine/taurine ratios were: chenodeoxycholic acid,
1.9; 7-ethyl analog, 0.3; and 7-propyl analog, 0.2. After oral
administration, during a 21-day feeding experiment, the 14C-labeled analogs
were recovered quantitatively in the feces. Chenodeoxycholic acid was
largely 7-dehydroxylated to lithocholic acid in the intestinal tract. In
contrast, the 7 alpha-hydroxy group of the 7-alkyl bile acids was
completely resistant to bacterial action. 7- Ethyl-chenodeoxycholic acid
was transformed in part to a compound tentatively identified as 7
alpha-hydroxy-3-oxo- 7 beta-ethyl-5 beta- cholanoic acid while
7-propyl-chenodeoxycholic acid was excreted unchanged. In the hamsters
used, the 7-alkyl bile acid analogs did not inhibit the bacterial
dehydroxylation of chenodeoxycholic acid. At the end of the 21-day feeding
period, analysis of the gallbladder bile showed that 7-methyl-, 7-ethyl-,
and 7-propyl-chenodeoxycholic acids accounted for 38, 31, and 12% of total
bile acids, respectively. The 7- alkyl bile acids decreased cholesterol
absorption; the 7-propyl analog caused significant decrease in serum and
liver cholesterol concentration. These experiments demonstrate that the
7-ethyl- and 7- propyl chenodeoxycholic acids, just like the
7-methyl-analog, are absorbed by the intestine and participate in the
enterohepatic circulation.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Metabolism of 7 beta-alkyl chenodeoxycholic acid analogs and their effect on cholesterol metabolism in hamsters
Institute of Pharmaceutical Science, Hiroshima University School of Medicine, Japan.
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