Literature DB >> 5480857

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

D C Collins, H D Robinson, C M Howard, J R Preedy.   

Abstract

In order to study the splanchnic metabolism of blood-borne estrogens, a constant infusion of estrone-6,7-(3)H was made in a series of dogs, and arteriovenous (A-V) differences at equilibrium were determined for estrone-6,7-(3)H and for its products estradiol-17beta, estrone sulfate, estrone glucosiduronate, and estradiol-17beta glucosiduronate across the splanchnic bed (artery-hepatic vein), the small intestine (artery-superior mesenteric vein), and the spleen (artery-splenic vein). Per cent extractions (100 - [V/A] 100) were calculated. The plasma metabolic clearance rate (MCR) for estrone was measured. Principal findings were as follows: mean MCR was 731 liters/day per m(2), SEM 50. By comparison with estimated hepatic plasma flow and using the observed splanchnic extraction of estrone, 45-71% of estrone metabolism was calculated to be extrasplanchnic. The significant mean per cent extractions were as follows (SEM in parentheses): splanchnic bedestrone 85.9 (1.92), estradiol-17beta 88.11 (3.36), estrone sulfate 27.9 (5.22), estrone glucosiduronate -48.5 (9.33), estradiol-17beta glucosiduronate -33.3 (80.3); small intestine-estrone 45.3 (2.60), estradiol-17beta 46.1 (12.9), estrone glucosiduronate - 30.8 (7.9); spleen-estrone 35 (3.8), estrone glucosiduronate 12 (3.7). These results lead to the following conclusions. Both estrone and estradiol-17beta are nearly completely extracted in one passage through the splanchnic bed. There is net uptake of estrone sulfate and net production of estrone glucosiduronate and of estradiol-17beta glucosiduronate by the splanchnic bed. There is net uptake of estrone and of estradiol-17beta by the intestine, associated with substantial net production of estrone glucosiduronate. There is net uptake of estrone by the spleen and a small but significant net uptake of estrone glucosiduronate.

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Year:  1970        PMID: 5480857      PMCID: PMC322733          DOI: 10.1172/JCI106451

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


  33 in total

1.  The determination of estrone, estradiol-17 beta, and estriol in urine and plasma with column partition chromatography.

Authors:  J R PREEDY; E H AITKEN
Journal:  J Biol Chem       Date:  1961-05       Impact factor: 5.157

2.  THEORY OF THE USE OF ARTERIOVENOUS CONCENTRATION DIFFERENCES FOR MEASURING METABOLISM IN STEADY AND NON-STEADY STATES.

Authors:  K L Zierler
Journal:  J Clin Invest       Date:  1961-12       Impact factor: 14.808

3.  15-alpha-hydroxyestrone "sulfate": a biliary metabolite of estrone sulfate in the non-pregnant female.

Authors:  H Jirku; U Hogsander; M Levitz
Journal:  Biochim Biophys Acta       Date:  1967-06-06

4.  Intermediates in the transformation of oral estradiol.

Authors:  J Fishman; S Goldberg; R S Rosenfeld; B Zumoff; L Hellman; T F Gallagher
Journal:  J Clin Endocrinol Metab       Date:  1969-01       Impact factor: 5.958

5.  Sites of in vivo extraction and interconversion of testosterone and androstenedione in dogs.

Authors:  A Chapdelaine
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808

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

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

7.  The synthesis of oestrogen monoglucuronides.

Authors:  J S Elce; J G Carpenter; A E Kellie
Journal:  J Chem Soc Perkin 1       Date:  1967

8.  [Resorption, metabolism and transport of estradiol-(17-beta) and estradiol (17-beta)-3-monosulfate in small intestine of rat].

Authors:  B P Lisboa; I Drossé; H Breuer
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1965

9.  Estrogen metabolism in the male dog. Uptake and disappearance of specific radioactive estrogens in tissues and plasma following estrone-6,7-3H administration. Identification of estriol-16-alpha, 17-alpha in tissues and urine.

Authors:  H Balikian; J Southerland; C M Howard; J R Preedy
Journal:  Endocrinology       Date:  1968-03       Impact factor: 4.736

10.  Studies on phenolic steroids in human subjects. II. The metabolic fate and hepato-biliary-enteric circulation of C14-estrone and C14-estradiol in women.

Authors:  A A SANDBERG; W R SLAUNWHITE
Journal:  J Clin Invest       Date:  1957-08       Impact factor: 14.808

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