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Biliary Excretion of Radioactivity After Intravenous Administration of 3H-1,25-dihydroxyvitamin D3 in Man

Overview
Journal Gut
Specialty Gastroenterology
Date 1985 Nov 1
PMID 3840765
Citations 6
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Abstract

Biliary radioactivity excretion was studied in 10 patients with postcholecystectomy T-tube drainage after intravenous administration of 3H-1,25-dihydroxyvitamin D3. The mean +/- SD radioactivity excreted in T-tube bile expressed as a percentage of the administered dose was 18.9 +/- 10.7% per 24 hours. After correction for incomplete bile collection the value obtained was 28.8 +/- 12.8%. The mean chloroform solubility of the biliary radioactivity increased from 17.0 +/- 8.4% to 69.4 +/- 15.1% after incubation with beta-glucuronidase. High performance liquid chromatography of chloroform extracts of bile revealed that most of the eluted radioactivity was more polar than 1,25(OH)2D3. The percentage radioactivity eluting as 3H-1,25(OH)2D3 increased from approximately 2.4 +/- 1.9 to 16.2 +/- 8.0 after incubation with beta-glucuronidase. We conclude that significant amounts of intravenously administered 3H-1,25(OH)2D3 are excreted in bile, mostly as more polar metabolites. The increase in free 3H-1,25(OH)2D3 after incubation with beta-glucuronidase indicates that glucuronides of 1,25(OH)2D3 are present in bile.

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References
1.
Avioli L, Lee S, McDonald J, Lund J, DeLuca H . Metabolism of vitamin D3-3H in human subjects: distribution in blood, bile, feces, and urine. J Clin Invest. 1967; 46(6):983-92. PMC: 297103. DOI: 10.1172/JCI105605. View

2.
BLIGH E, Dyer W . A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959; 37(8):911-7. DOI: 10.1139/o59-099. View

3.
Bell P, KODICEK E . Investigations on metabolites of vitamin D in rat bile. Separation and partial identification of a major metabolite. Biochem J. 1969; 115(4):663-9. PMC: 1185191. DOI: 10.1042/bj1150663. View

4.
Holick M, Schnoes H, Kasten P, Boyle I, DeLuca H . 1,24,25-Trihydroxyvitamin D3. A metabolite of vitamin D3 effective on intestine. J Biol Chem. 1973; 248(19):6691-6. View

5.
Edelstein S, Charman M, LAWSON D, KODICEK E . Competitive protein-binding assay for 25-hydroxycholecalciferol. Clin Sci Mol Med. 1974; 46(2):231-40. DOI: 10.1042/cs0460231. View