Abstract
Vitamin D3-3H has been administered intravenously to seven normal subjects, three patients with biliary fistulas, and four patients with cirrhosis. Plasma D3-3H half-times normally ranged from 20 to 30 hours. in vivo evidence that a metabolic transformation of vitamin D occurs was obtained, and a polar biologically active vitamin D metabolite was isolated from plasma.
Urinary radioactivity averaged 2.4% of the administered dose for the 48-hour period after infusion, and all the excreted radioactivity represented chemically altered metabolites of vitamin D. The metabolites in urine were mainly water-soluble, with 26% in conjugated form.
From 3 to 6% of the injected radioactivity was excreted in the bile of subjects with T-tube drainage and 5% in the feces of patients having no T-tube. The pattern of fecal and biliary radioactivity suggested that the passage of vitamin D and its metabolites from bile into the intestine represents an essential stage for the fecal excretion of vitamin D metabolites in man.
Abnormally slow plasma disappearance of vitamin D3-3H in patients with cirrhosis was associated with a significant decrease in the quantity and rate of glucuronide metabolite excretion in the urine.
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- ATKINSON M., NORDIN B. E., SHERLOCK S. Malabsorption and bone disease in prolonged obstructive jaundice. Q J Med. 1956 Jul;25(99):299–312. [PubMed] [Google Scholar]
- BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
- BRADLOW H. L., FRAZELL E. L., GALLAGHER T. F., HELLMAN L. Tracer studies of the absorption and fate of steroid hormones in man. J Clin Invest. 1956 Sep;35(9):1033–1044. doi: 10.1172/JCI103349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Callow R. K., Kodicek E., Thompson G. A. Metabolism of tritiated vitamin D. Proc R Soc Lond B Biol Sci. 1966 Feb 15;164(994):1–20. doi: 10.1098/rspb.1966.0010. [DOI] [PubMed] [Google Scholar]
- Chen P. S., Jr, Lane K. Serum protein binding of vitamin D3. Arch Biochem Biophys. 1965 Oct;112(1):70–75. doi: 10.1016/0003-9861(65)90011-1. [DOI] [PubMed] [Google Scholar]
- KELLY R. G., PEETS E. A., GORDON S., BUYSKE D. A. Determination of C-14 and H3 in biological samples by Schoeniger combustion and liquid scintillation techniques. Anal Biochem. 1961 Jun;2:267–273. doi: 10.1016/s0003-2697(61)80010-9. [DOI] [PubMed] [Google Scholar]
- LEVVY G. A. The preparation and properties of beta-glucuronidase. IV. Inhibition by sugar acids and their lactones. Biochem J. 1952 Nov;52(3):464–472. doi: 10.1042/bj0520464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lund J., DeLuca H. F. Biologically active metabolite of vitamin D3 from bone, liver, and blood serum. J Lipid Res. 1966 Nov;7(6):739–744. [PubMed] [Google Scholar]
- NORMAN A. W., DELUCA H. F. THE PREPARATION OF H3-VITAMINS D2 AND D3--THEIR LOCALIZATION IN THE RAT. Biochemistry. 1963 Sep-Oct;2:1160–1168. doi: 10.1021/bi00905a044. [DOI] [PubMed] [Google Scholar]
- NORMAN A. W., DELUCA H. F. THE SUBCELLULAR LOCATION OF H3 VITAMIN D3 IN KIDNEY AND INTESTINE. Arch Biochem Biophys. 1964 Jul;107:69–77. doi: 10.1016/0003-9861(64)90270-x. [DOI] [PubMed] [Google Scholar]
- NORMAN A. W., LUND J., DELUCA H. F. BIOLOGICALLY ACTIVE FORMS OF VITAMIN D3 IN KIDNEY AND INTESTINE. Arch Biochem Biophys. 1964 Oct;108:12–21. doi: 10.1016/0003-9861(64)90349-2. [DOI] [PubMed] [Google Scholar]
- Nair P. P., Bucana C. Intracellular distribution of vitamin D in rat liver. Biochim Biophys Acta. 1966 Aug 24;124(2):254–259. doi: 10.1016/0304-4165(66)90187-5. [DOI] [PubMed] [Google Scholar]
- Neville P. F., DeLuca H. F. The synthesis of [1,2-3H]vitamin D3 and the tissue localization of a 0.25-mu-g (10 IU) dose per rat. Biochemistry. 1966 Jul;5(7):2201–2207. doi: 10.1021/bi00871a007. [DOI] [PubMed] [Google Scholar]
- PETERSON R. E. Adrenocortical steroid metabolism and adrenal cortical function in liver disease. J Clin Invest. 1960 Feb;39:320–331. doi: 10.1172/JCI104043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SANDBERG A. A., SLAUNWHITE W. R., Jr Metabolism of 4-C14-testosterone in human subjects. I. Distribution in bile, blood, feces and urine. J Clin Invest. 1956 Dec;35(12):1331–1339. doi: 10.1172/JCI103389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SCHACHTER D., FINKELSTEIN J. D., KOWARSKI S. METABOLISM OF VITAMIN D. I. PREPARATION OF RADIOACTIVE VITAMIN D AND ITS INTESTINAL ABSORPTION IN THE RAT. J Clin Invest. 1964 May;43:787–796. doi: 10.1172/JCI104965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson G. R., Lewis B., Booth C. C. Absorption of vitamin D3-3H in control subjects and patients with intestinal malabsorption. J Clin Invest. 1966 Jan;45(1):94–102. doi: 10.1172/JCI105327. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zull J. E., Czarnowska-Misztal E., Deluca H. F. Actinomycin D Inhibition of Vitamin D Action. Science. 1965 Jul 9;149(3680):182–184. doi: 10.1126/science.149.3680.182. [DOI] [PubMed] [Google Scholar]