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Bile Acid Composition in Brown Pigment Stones

Overview
Journal Dig Dis Sci
Specialty Gastroenterology
Date 1990 Jan 1
PMID 2295290
Citations 7
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Abstract

The bile acids in brown pigment stones and gallbladder bile were fractionated into free acids, glycine and taurine conjugates, and sulfates using diethylaminohydroxypropyl Sephadex LH-20 (DEAP-LH-20) column chromatography and were quantitated by gas chromatography. Twenty-eight cases of brown pigment stones were studied and divided into two groups: those with and those without bacteria possessing bile acid-deconjugating activity. In the former, free bile acid amounted to 62 +/- 34% of the total bile acid, while in the latter, only 0.1% of total bile acid was free bile acid. The fraction of total bile acid made up of free bile acids was found to be consistently higher in brown pigment stones than in the corresponding bile, irrespective of the presence or absence of biliary infection. Free bile acid is present in negligible amounts in normal bile. Total bile acid concentration in the bile of patients with brown pigment stones was significantly less than that of controls (13 vs 50 mg/ml). Biliary infection is almost always present in cases with brown pigment stones. These findings suggest that bacterial infection is present at the initiation of brown pigment stone formation as well as during the period of ensuing stone growth.

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References
1.
Nair P, Gordon M, REBACK J . The enzymatic cleavage of the carbon-nitrogen bond in 3-alpha, 7-alpha, 12-alpha-trihydroxy-5-beta-cholan-24-oylglycine. J Biol Chem. 1967; 242(1):7-11. View

2.
Furusawa T . [Surface-chemical studies on the stability of human bile]. Fukuoka Igaku Zasshi. 1962; 53:124-65. View

3.
Onochi S, Masu A, Takahashi W, Suzuki N . [Study on bile acid and lipid of gallbladder bile and gallstone in cases with calcium bilirubinate stones]. Nihon Shokakibyo Gakkai Zasshi. 1984; 81(10):2552-60. View

4.
Soloway R, Trotman B, Ostrow J . Pigment gallstones. Gastroenterology. 1977; 72(1):167-82. View

5.
Ostrow J, Celic L, MUKERJEE P . Molecular and micellar associations in the pH-dependent stable and metastable dissolution of unconjugated bilirubin by bile salts. J Lipid Res. 1988; 29(3):335-48. View