Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1988 Mar 1;250(2):527–532. doi: 10.1042/bj2500527

Assay and properties of 25-hydroxyvitamin D3 23-hydroxylase. Evidence that 23,25-dihydroxyvitamin D3 is a major metabolite in 1,25-dihydroxyvitamin D3-treated or fasted guinea pigs.

J I Pedersen 1, Y Hagenfeldt 1, I Björkhem 1
PMCID: PMC1148887  PMID: 3355535

Abstract

Incubation of 25-hydroxyvitamin D3 with kidney cortex mitochondria from 1,25-dihydroxyvitamin D3-treated guinea pigs resulted in the formation of 23,25-dihydroxyvitamin D3 as the major product. The identity of the product was verified by g.c.-m.s. and quantification was performed by h.p.l.c. The rates of the reaction were in the range 1.0-1.8 pmol/min per mg of mitochondrial protein (at 37 degrees C), which were 5-10 times the rates of formation of 24,25-dihydroxyvitamin D3. In mitochondrial preparations from untreated guinea pigs, the rate of 23-hydroxylation was below detection limit (0.02 pmol/min per mg of mitochondrial protein). Fasting the animals for 24 h induced the 23-hydroxylase almost as efficiently as treatment with 1,25-dihydroxyvitamin D3, with a concomitant depression of the 1 alpha-hydroxylase. The 23-hydroxylase reaction required oxidizable substrate, was decreased by low O2 partial pressures and inhibited by CO or the uncoupler carbonyl cyanide p-trifluoromethoxyphenylhydrazone. It was stimulated by the respiratory-chain inhibitors rotenone, antimycin A and KCN. These results indicate that the guinea-pig renal mitochondrial 23-hydroxylase is a cytochrome P-450 and that the reducing equivalents are primarily supplied by NADPH via the energy-dependent transhydrogenase.

Full text

PDF
527

Selected References

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

  1. DeLuca H. F. Recent advances in the metabolism of vitamin D. Annu Rev Physiol. 1981;43:199–209. doi: 10.1146/annurev.ph.43.030181.001215. [DOI] [PubMed] [Google Scholar]
  2. DeLuca H. F., Schnoes H. K. Metabolism and mechanism of action of vitamin D. Annu Rev Biochem. 1976;45:631–666. doi: 10.1146/annurev.bi.45.070176.003215. [DOI] [PubMed] [Google Scholar]
  3. DeLuca H. F., Schnoes H. K. Vitamin D: recent advances. Annu Rev Biochem. 1983;52:411–439. doi: 10.1146/annurev.bi.52.070183.002211. [DOI] [PubMed] [Google Scholar]
  4. Delvin E. E., Dussault M. Kinetics of kidney mitochondrial 25-hydroxycholecalciferol-1 alpha-hydroxylase in vitamin D-repleted weanling guinea pigs. Arch Biochem Biophys. 1985 Jul;240(1):337–344. doi: 10.1016/0003-9861(85)90039-6. [DOI] [PubMed] [Google Scholar]
  5. Engstrom G. W., Reinhardt T. A., Horst R. L. 25-Hydroxyvitamin D3-23-hydroxylase, a renal enzyme in several animal species. Arch Biochem Biophys. 1986 Oct;250(1):86–93. doi: 10.1016/0003-9861(86)90704-6. [DOI] [PubMed] [Google Scholar]
  6. Fraser D. R., Kodicek E. Unique biosynthesis by kidney of a biological active vitamin D metabolite. Nature. 1970 Nov 21;228(5273):764–766. doi: 10.1038/228764a0. [DOI] [PubMed] [Google Scholar]
  7. Fraser D. R. Regulation of the metabolism of vitamin D. Physiol Rev. 1980 Apr;60(2):551–613. doi: 10.1152/physrev.1980.60.2.551. [DOI] [PubMed] [Google Scholar]
  8. Ghazarian J. G., Jefcoate C. R., Knutson J. C., Orme-Johnson W. H., DeLuca H. F. Mitochondrial cytochrome p450. A component of chick kidney 25-hydrocholecalciferol-1alpha-hydroxylase. J Biol Chem. 1974 May 25;249(10):3026–3033. [PubMed] [Google Scholar]
  9. Hagenfeldt Y., Pedersen J. I., Björkhem I. Properties of guinea-pig kidney 25-hydroxyvitamin D3 1 alpha-hydroxylase assayed by isotope dilution-mass spectrometry. Biochem J. 1988 Mar 1;250(2):521–526. doi: 10.1042/bj2500521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Holick M. F., Schnoes H. K., DeLuca H. F., Suda T., Cousins R. J. Isolation and identification of 1,25-dihydroxycholecalciferol. A metabolite of vitamin D active in intestine. Biochemistry. 1971 Jul 6;10(14):2799–2804. doi: 10.1021/bi00790a023. [DOI] [PubMed] [Google Scholar]
  11. Holmberg I., Saarem K., Pedersen J. I., Björkhem I. Assay of 25-hydroxy vitamin D3-1 alpha-hydroxylase in pig kidney mitochondria using isotope dilution-mass spectrometry. Anal Biochem. 1986 Dec;159(2):317–322. doi: 10.1016/0003-2697(86)90348-9. [DOI] [PubMed] [Google Scholar]
  12. Horst R. L. 25-OHD3-26,23-lactone: a metabolite of vitamin D3 that is 5 times more potent than 25-OHD3 in the rat plasma competitive protein binding radioassay. Biochem Biophys Res Commun. 1979 Jul 12;89(1):286–293. doi: 10.1016/0006-291x(79)90976-8. [DOI] [PubMed] [Google Scholar]
  13. Horst R. L., Shepard R. M., Jorgensen N. A., DeLuca H. F. The determination of 24,25-dihydroxyvitamin D and 25,26-dihydroxyvitamin D in plasma from normal and nephrectomized man. J Lab Clin Med. 1979 Feb;93(2):277–285. [PubMed] [Google Scholar]
  14. Ishizuka S., Ishimoto S., Norman A. W. Metabolic pathway to 25-hydroxyvitamin D3-26,23-lactone from 25-hydroxyvitamin D3. FEBS Lett. 1982 Feb 8;138(1):83–87. doi: 10.1016/0014-5793(82)80400-6. [DOI] [PubMed] [Google Scholar]
  15. Knutson J. C., DeLuca H. F. 25-Hydroxyvitamin D3-24-hydroxylase. Subcellular location and properties. Biochemistry. 1974 Mar 26;13(7):1543–1548. doi: 10.1021/bi00704a034. [DOI] [PubMed] [Google Scholar]
  16. MAKITA M., WELLS W. W. Quantitative analysis of fecal bile acids by gas-liquid chromatography. Anal Biochem. 1963 Jun;5:523–530. doi: 10.1016/0003-2697(63)90072-1. [DOI] [PubMed] [Google Scholar]
  17. Mayer E., Reddy G. S., Chandraratna R. A., Okamura W. H., Kruse J. R., Popjàk G., Bishop J. E., Norman A. W. 23,25-Dihydroxy-24-oxovitamin D3: a metabolite of vitamin D3 made in the kidney. Biochemistry. 1983 Apr 12;22(8):1798–1805. doi: 10.1021/bi00277a009. [DOI] [PubMed] [Google Scholar]
  18. Napoli J. L., Pramanik B. C., Partridge J. J., Uskoković M. R., Horst R. L. 23S,25-dihydroxyvitamin D3 as a circulating metabolite of vitamin D3. Its role in 25-hydroxyvitamin D3-26,23-lactone biosynthesis. J Biol Chem. 1982 Aug 25;257(16):9634–9639. [PubMed] [Google Scholar]
  19. Olson E. B., Jr, Knutson J. C., Bhattacharyya M. H., DeLuca H. F. The effect of hepatectomy on the synthesis of 25-hydroxyvitamin D3. J Clin Invest. 1976 May;57(5):1213–1220. doi: 10.1172/JCI108389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pedersen J. I., Shobaki H. H., Holmberg I., Bergseth S., Björkhem I. 25-Hydroxyvitamin D3-24-hydroxylase in rat kidney mitochondria. J Biol Chem. 1983 Jan 25;258(2):742–746. [PubMed] [Google Scholar]
  21. 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]
  22. Shephard R. M., Deluca H. F. Plasma concentrations of vitamin D3 and its metabolites in the rat as influenced by vitamin D3 or 25-hydroxyvitamin D3 intakes. Arch Biochem Biophys. 1980 Jun;202(1):43–53. doi: 10.1016/0003-9861(80)90404-x. [DOI] [PubMed] [Google Scholar]
  23. Suda T., DeLuca H. F., Schnoes H. K., Blunt J. W. The isolation and identification of 25-hydroxyergocalciferol. Biochemistry. 1969 Sep;8(9):3515–3520. doi: 10.1021/bi00837a005. [DOI] [PubMed] [Google Scholar]
  24. Tahaka Y., Lorenc R. S., DeLuca H. F. The role of 1,25-dihydroxyvitamin D3 and parathyroid hormone in the regulation of chick renal 25-hydroxyvitamin D3-24-hydroxylase. Arch Biochem Biophys. 1975 Dec;171(2):521–526. doi: 10.1016/0003-9861(75)90061-2. [DOI] [PubMed] [Google Scholar]
  25. Tanaka Y., DeLuca H. F., Schnoes H. K., Ikekawa N., Eguchi T. 23,25-Dihydroxyvitamin D3: a natural precursor in the biosynthesis of 25-hydroxyvitamin D3-26,23-lactone. Proc Natl Acad Sci U S A. 1981 Aug;78(8):4805–4808. doi: 10.1073/pnas.78.8.4805. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tanaka Y., DeLuca H. F. Stimulation of 24,25-dihydroxyvitamin D3 production by 1,25-dihydroxyvitamin D3. Science. 1974 Mar;183(130):1198–1200. doi: 10.1126/science.183.4130.1198. [DOI] [PubMed] [Google Scholar]
  27. Tanaka Y., Shepard R. A., DeLuca H. F., Schnoes H. K. The 26-hydroxylation of 25-hydroxyvitamin D3 in vitro by chick renal homogenates. Biochem Biophys Res Commun. 1978 Jul 14;83(1):7–13. doi: 10.1016/0006-291x(78)90390-x. [DOI] [PubMed] [Google Scholar]
  28. Tanaka Y., Wichmann J. K., Schnoes H. K., DeLuca H. F. Isolation and identification of 23,25-dihydroxyvitamin D3, an in vivo metabolite of vitamin D3. Biochemistry. 1981 Jun 23;20(13):3875–3879. doi: 10.1021/bi00516a032. [DOI] [PubMed] [Google Scholar]
  29. Wichmann J. K., DeLuca H. F., Schnoes H. K., Horst R. L., Shepard R. M., Jorgensen N. A. 25-Hydroxyvitamin D3 26,23-lactone: a new in vivo metabolite of vitamin D. Biochemistry. 1979 Oct 30;18(22):4775–4780. doi: 10.1021/bi00589a002. [DOI] [PubMed] [Google Scholar]
  30. Yamada S., Ino E., Takayama H., Horiuchi N., Shinki T., Suda T., Jones G., DeLuca H. F. Differences in the side-chain metabolism of vitamin D3 between chickens and rats. Proc Natl Acad Sci U S A. 1985 Nov;82(22):7485–7489. doi: 10.1073/pnas.82.22.7485. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES