Literature DB >> 4303458

Studies on phenolic steroids in human subjects. 8. Metabolism of estriol-16 alpha-glucosiduronate.

N Inoue, A A Sandberg, J B Graham, W R Slaunwhite.   

Abstract

6,7-(3)H-Estriol-16alpha-glucosiduronate-(14)C was administered to eight women (nine studies) by several routes: both injection and infusion (300 min) into the cubital vein, injection into the portal vein system, ingestion and instillation into the duodenum, jejunum, and ileum. Urine, collected from 0-2, 2-4, 4-8, 8-12, and 12-24 hr, was analyzed by countercurrent distribution for its content of radioactive 3- and 16-glucosiduronate (E(3)-3Gl,E(3)-16Gl) and sulfoglucosiduronate (E(3)-3S,16Gl) of estriol as well as for (3)H/(14)C ratio of each conjugate. After peripheral injection 50-60% of the injected E(3)-16Gl was excreted unchanged along with about 5% as E(3)-3S,16Gl with an unchanged (3)H/(14)C ratio, indicating direct sulfation of the injected E(3)-16Gl. During a 300 min infusion, urinary excretion closely resembled that following injection. But 2-4 hr after the end of the infusion excretion of E(3)-3S, 16Gl stopped, excretion of E(3)-3Gl (17%/24 hr) with an elevated (3)H/(14)C ratio started, and excretion of E(3)-16Gl continued (70%/24 hr), but with a rapidly increasing (3)H/(14)C ratio. This indicated sequestration in a sluggishly metabolizing compartment where two processes occurred: (a) extensive hydrolysis of E(3)-16Gl followed by reconjugation at either C3 or C16 with unlabeled uridine diphosphate glucuronic acid (UDPGA), thereby increasing the (3)H/(14)C ratio; and (b) transconjugation from C16 to C3, thereby producing E(3)-3Gl with finite (3)H/(14)C ratios. Instillation into various segments of the small intestine produced results qualitatively similar to those after intravenous infusion, whereas ingestion and intraportal injection resembled peripheral intravenous injection. Therefore, we have postulated the possibility of an enteric circulation (in addition to an enterohepatic circulation) in which the steroid or its conjugates are transported into the small intestine in the succus entericus, modified, and then reabsorbed and excreted in the urine-a process which requires several hours.

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Year:  1969        PMID: 4303458      PMCID: PMC322230          DOI: 10.1172/JCI105995

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  19 in total

1.  Biliary and urinary metabolites of estriol-15-3H-3-sulfate-35S in women.

Authors:  S Emerman; G H Twombly; M Levitz
Journal:  J Clin Endocrinol Metab       Date:  1967-04       Impact factor: 5.958

2.  Permeability characteristics of the human small intestine.

Authors:  J S Fordtran; F C Rector; M F Ewton; N Soter; J Kinney
Journal:  J Clin Invest       Date:  1965-12       Impact factor: 14.808

3.  [Biogenesis of estriol-16-alpha-monoglucuronide and estriol-17beta-monoglucuronide].

Authors:  K Dahn; H Brewer
Journal:  Acta Endocrinol (Copenh)       Date:  1966-05

4.  Interdependence of routes excreting manganese.

Authors:  A J Bertinchamps; S T Miller; G C Cotzias
Journal:  Am J Physiol       Date:  1966-07

5.  The biosynthesis of labeled estriol-3-sulfate-16-glucosiduronate.

Authors:  M Levitz; J Katz; G H Twombly
Journal:  Steroids       Date:  1965-11       Impact factor: 2.668

6.  Biosynthesis of radioactive estriol-3-glucosiduronate by guinea pig liver homogenate.

Authors:  U Goebelsmann; E Diczfalusy; J Katz; M Levitz
Journal:  Steroids       Date:  1965-12       Impact factor: 2.668

7.  Oestriol-3-glucosiduronate, a major urinary metabolite of oestriol and oestriol-16(17?)-glucosiduronate.

Authors:  U Goebelsmann; K Sjöberg; N Wiqvist; E Diczfalusy
Journal:  Acta Endocrinol (Copenh)       Date:  1965-10

8.  The quantitative relationship of oestrogen-3-glucosiduronates and oestrogen-16 (or 17)-glucosiduronates in human late pregnancy urine.

Authors:  R Hähnel
Journal:  J Endocrinol       Date:  1967-08       Impact factor: 4.286

9.  Comparison of the metabolism of oestriol-3-glucosiduronate and oestriol-16-glucosiduronate in pregnant women.

Authors:  U Goebelsmann; I Cooke; N Wiqvist; E Diczfalusy
Journal:  Acta Endocrinol (Copenh)       Date:  1966-05

10.  Absorption of L-methionine from the human small intestine.

Authors:  H P Schedl; C E Pierce; A Rider; J A Clifton
Journal:  J Clin Invest       Date:  1968-02       Impact factor: 14.808

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  3 in total

1.  Studies on the metabolism of 5alpha-androst-16-en-3-one in boar tests in vivo.

Authors:  Y A Saat; D B Gower; F A Harrison; R B Heap
Journal:  Biochem J       Date:  1974-11       Impact factor: 3.857

2.  Studies on phenolic steroids in human subjects. IX. Role of the intestine in the conjugation of estriol.

Authors:  N Inoue; A A Sandberg; J B Graham; W R Slaunwhite
Journal:  J Clin Invest       Date:  1969-02       Impact factor: 14.808

3.  Metabolism of arterial plasma estrogens by the splanchnic organs of the dog in vivo.

Authors:  D C Collins; H D Robinson; C M Howard; J R Preedy
Journal:  J Clin Invest       Date:  1970-12       Impact factor: 14.808

  3 in total

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