Abstract
Bile acid kinetics and biliary lipid composition were characterized in six women with gallstones before and after 6 mo of oral therapy with chenodeoxycholic acid, an agent that induces dissolution of cholesterol gallstones in man. Over a dosage range of 1-4 g/day, absorption varied from 0.8 to 2.3 g/day. The chenodeoxycholic acid pool expanded two-to sixfold, and bile became composed predominantly (> 90%) of chenodeoxycholic acid conjugated chiefly with glycine. Cholic acid and deoxycholic acid pools decreased markedly, so that the total bile acid pool expanded much less, about twofold on the average. Cholic acid synthesis decreased in five of the six patients, consistent with negative feedback inhibition of cholic acid synthesis by chenodeoxycholic acid. In four patients whose bile was above or close to saturation with cholesterol, the bile became unsaturated; in two patients, whose bile was unsaturated, it remained so. In five patients with radiolucent gallstones, chenodeoxycholic acid therapy was continued after completion of kinetic and composition measurements; the stones decreased in size or dissolved entirely during the subsequent 6 to 18 mo. Similar measurements of bile acid kinetics and biliary lipid composition were made before and after a 6-mo period without medication in a control group of six healthy women; no changes occurred.
MeSH Terms
Administration, Oral
Bile/analysis
Bile Acids and Salts/metabolism
Carbon Radioisotopes
Chenodeoxycholic Acid/administration & dosage,metabolism,pharmacology,therapeutic use
Cholelithiasis/drug therapy,metabolism
Cholesterol/analysis
Cholic Acids/metabolism
Chromatography, Gas
Chromatography, Thin Layer
Deoxycholic Acid/metabolism
Feces/analysis
Female
Humans
Lipids/analysis
Lithocholic Acid/metabolism
Radioisotope Dilution Technique
Tritium
Chemicals
Bile Acids and Salts
Carbon Radioisotopes
Cholic Acids
Lipids
Deoxycholic Acid
Chenodeoxycholic Acid
Tritium
Lithocholic Acid
Cholesterol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Danzinger R C
Hofmann A F
Thistle J L
Schoenfield L J
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