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. 1979 Sep 15;182(3):745–750. doi: 10.1042/bj1820745

The metabolism of cholecalciferol in the liver of Japanese quail (Coturnix coturnix japonica) with particular reference to the effects of oestrogen.

R A Nicholson, M Akhtar, T G Taylor
PMCID: PMC1161408  PMID: 229826

Abstract

1. Studies were carried out in vitro with the livers of Japanese quail that had been fed from hatching on diets supplying their full requirements for vitamin D. 2. 25-Hydroxycholecalciferol was the major metabolite when liver homogenates of egg-laying female and oestrogen-treated quail of both sexes were incubated with [3H]cholecalciferol. 3. Very little 25-hydroxycholecalciferol was generated from liver homogenates of adult male and immature quail. Instead the cholecalciferol was converted into one or more compounds less polar than 25-hydroxycholecalciferol and into a number of highly polar metabolites, some of which were water-soluble. 4. Oestrogen not only stimulated the 25-hydroxylation of cholecalciferol but also protected both cholecalciferol and 25-hydroxycholecalciferol from degradation by the enzymic pathways active in immature and male birds. 5. These actions of oestrogen may be of physiological significance in relation to the high requirements of laying birds for 1,25-dihydroxycholecalciferol to support the intense metabolism of calcium associated with egg-shell calcification.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. 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]
  2. Baksi S. N., Kenny A. D. Vitamin D metabolism in Japanese quail: gonadal hormones and dietary calcium effects. Am J Physiol. 1978 Jun;234(6):E622–E628. doi: 10.1152/ajpendo.1978.234.6.E622. [DOI] [PubMed] [Google Scholar]
  3. Bhattacharyya M. H., DeLuca H. F. The regulation of calciferol-25-hydroxylase in the chick. Biochem Biophys Res Commun. 1974 Jul 24;59(2):734–741. doi: 10.1016/s0006-291x(74)80041-0. [DOI] [PubMed] [Google Scholar]
  4. CHAIKOFF I. L., ENTENMAN C., HILLYARD L. A. Concentration and composition of serum lipoproteins of cholesterol-fed and stilbestrol-injected birds. J Biol Chem. 1956 Nov;223(1):359–368. [PubMed] [Google Scholar]
  5. Corradino R. A. Embryonic chick intestine in organ culture: response to vitamin D 3 and its metabolites. Science. 1973 Jan 26;179(4071):402–405. doi: 10.1126/science.179.4071.402. [DOI] [PubMed] [Google Scholar]
  6. Corradino R. A., Fullmer C. S., Wasserman R. H. Embryonic chick intestine in organ culture: stimulation of calcium transport by exogenous vitamin D-induced calcium-binding protein. Arch Biochem Biophys. 1976 Jun;174(2):738–743. doi: 10.1016/0003-9861(76)90404-5. [DOI] [PubMed] [Google Scholar]
  7. Holick M. F., Clark M. B. The photobiogenesis and metabolism of vitamin D. Fed Proc. 1978 Oct;37(12):2567–2574. [PubMed] [Google Scholar]
  8. Ponchon G., Kennan A. L., DeLuca H. F. "Activation" of vitamin D by the liver. J Clin Invest. 1969 Nov;48(11):2032–2037. doi: 10.1172/JCI106168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. TAYLOR T. G. CALCIUM-ENDOCRINE RELATIONSHIPS IN THE LAYING HEN. Proc Nutr Soc. 1965;24:49–54. [PubMed] [Google Scholar]
  10. Tanaka Y., Castillo L., DeLuca H. F. Control of renal vitamin D hydroxylases in birds by sex hormones. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2701–2705. doi: 10.1073/pnas.73.8.2701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Tucker G., 3rd, Gagnon R. E., Haussler M. R. Vitamin D 3 -25-hydroxylase: tissue occurrence and apparent lack of regulation. Arch Biochem Biophys. 1973 Mar;155(1):47–57. doi: 10.1016/s0003-9861(73)80008-6. [DOI] [PubMed] [Google Scholar]

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