Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1988 Oct 1;255(1):91–97. doi: 10.1042/bj2550091

The calcium ionophore A23187 is a potent stimulator of the vitamin D3-25 hydroxylase in hepatocytes isolated from normocalcaemic vitamin D-depleted rats.

N Benbrahim 1, C Dubé 1, S Vallieres 1, M Gascon-Barré 1
PMCID: PMC1135194  PMID: 2848514

Abstract

The role played by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3] and/or by calcium on the C-25 hydroxylation of vitamin D3 (D3) was studied in hepatocytes isolated from D-depleted rats which were divided into four treatment groups: Group 1 served as controls, Group 2 received calcium gluconate, Groups 3 and 4 were infused with 1,25(OH)2D3 at 7 and 65 pmol/24 h x 7 days respectively. The treatments normalized serum calcium in all but the controls which remained hypocalcaemic, while serum 1,25(OH)2D3 remained low in Groups 1 and 2 but increased to physiologic and supraphysiologic levels in Groups 3 and 4. The data show that basal D3-25 hydroxylase activities were not significantly affected by any of the treatments. Addition of CaCl2, EGTA, or Quin-2 in vitro revealed that relative to basal values, EGTA strongly inhibited the enzyme activity in all groups (P less than 0.0001), except in G 1; Quin-2 and CaCl2 had no significant effect on the activity of the enzyme in any of the groups. Addition of 1,25(OH)2D3 or A23187 in vitro in the presence of CaCl2 revealed that 1,25(OH)2D3 did not significantly affect enzyme activity, while A23187 was found to stimulate its activity in vitamin D-depleted animals, but most specifically in Group 2 (P less than 0.001); low serum calcium (Group 1) dampened (P less than 0.01), and 1,25(OH)2D3 treatment in vivo totally blunted (P less than 0.001) the response to A23187. The data suggest that 1,25(OH)2D3 supplementation in vivo has per se little or no effect on the basal D3-25 hydroxylase activity. The data show, however, that the magnitude of the response to various challenges in vitro is greatly influenced by the conditioning in vivo of the animals. They also show that A23187 can be a potent stimulator of the enzyme activity, which allowed us to demonstrate a significant reserve for the C-25 hydroxylation of D3 which is well expressed in hepatocytes obtained from D-depleted calcium-supplemented rats.

Full text

PDF
91

Selected References

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

  1. Baran D. T., Milne M. L. 1,25 Dihydroxyvitamin D increases hepatocyte cytosolic calcium levels. A potential regulator of vitamin D-25-hydroxylase. J Clin Invest. 1986 May;77(5):1622–1626. doi: 10.1172/JCI112478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baran D. T., Milne M. L. 1,25 dihydroxyvitamin D-induced inhibition of 3H-25 hydroxyvitamin D production by the rachitic rat liver in vitro. Calcif Tissue Int. 1983 Jul;35(4-5):461–464. doi: 10.1007/BF02405077. [DOI] [PubMed] [Google Scholar]
  3. Bell N. H., Shaw S., Turner R. T. Evidence that 1,25-dihydroxyvitamin D3 inhibits the hepatic production of 25-hydroxyvitamin D in man. J Clin Invest. 1984 Oct;74(4):1540–1544. doi: 10.1172/JCI111568. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bell N. H., Shaw S., Turner R. T. Evidence that calcium modulates circulating 25-hydroxyvitamin D in man. J Bone Miner Res. 1987 Jun;2(3):211–214. doi: 10.1002/jbmr.5650020307. [DOI] [PubMed] [Google Scholar]
  5. Berlin T., Björkhem I. On the regulatory importance of 1,25-dihydroxyvitamin D3 and dietary calcium on serum levels of 25-hydroxyvitamin D3 in rats. Biochem Biophys Res Commun. 1987 Apr 29;144(2):1055–1058. doi: 10.1016/s0006-291x(87)80071-2. [DOI] [PubMed] [Google Scholar]
  6. Berry M. N., Friend D. S. High-yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structural study. J Cell Biol. 1969 Dec;43(3):506–520. doi: 10.1083/jcb.43.3.506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bhattacharyya M. H., DeLuca H. F. The regulation of rat liver calciferol-25-hydroxylase. J Biol Chem. 1973 May 10;248(9):2969–2973. [PubMed] [Google Scholar]
  8. Chisholm J. C., Kim S., Tashjian A. H., Jr Modulation by 1,25-dihydroxycholecalciferol of the acute change in cytosolic free calcium induced by thyrotropin-releasing hormone in GH4C1 pituitary cells. J Clin Invest. 1988 Mar;81(3):661–668. doi: 10.1172/JCI113370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Clements M. R., Johnson L., Fraser D. R. A new mechanism for induced vitamin D deficiency in calcium deprivation. Nature. 1987 Jan 1;325(6099):62–65. doi: 10.1038/325062a0. [DOI] [PubMed] [Google Scholar]
  10. Corlett S. C., Chaudhary M. S., Tomlinson S., Care A. D. The involvement of intracellular calcium ion concentration and calmodulin in the 25-hydroxylation of cholecalciferol in ovine and rat liver. Cell Calcium. 1987 Aug;8(4):247–258. doi: 10.1016/0143-4160(87)90001-7. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. GUROFF G., DELUCA H. F., STEENBOCK H. Citrate and action of vitamin D on calcium and phosphorus metabolism. Am J Physiol. 1963 May;204:833–836. doi: 10.1152/ajplegacy.1963.204.5.833. [DOI] [PubMed] [Google Scholar]
  13. Gascon-Barré M., Elbaz H., Therrien-Ferland D. Sequestration and microsomal C-25 hydroxylation of [3H]-vitamin D3 by the rat liver. Metabolism. 1985 Mar;34(3):244–250. doi: 10.1016/0026-0495(85)90007-1. [DOI] [PubMed] [Google Scholar]
  14. Gascon-Barré M., Huet P. M. Role of the liver in the homeostasis of calciferol metabolism in the dog. Endocrinology. 1982 Feb;110(2):563–570. doi: 10.1210/endo-110-2-563. [DOI] [PubMed] [Google Scholar]
  15. Gindler E. M., King J. D. Rapid colorimetric determination of calcium in biologic fluids with methylthymol blue. Am J Clin Pathol. 1972 Oct;58(4):376–382. doi: 10.1093/ajcp/58.5.376. [DOI] [PubMed] [Google Scholar]
  16. Haddad P., Coulombe P. A., Gascon-Barré M. Influence of the vitamin D hormonal status on the hepatic response to bromobenzene. J Pharmacol Exp Ther. 1987 Jul;242(1):354–363. [PubMed] [Google Scholar]
  17. Haddad P., Gascon-Barré M., Brault G., Plourde V. Influence of calcium or 1,25-dihydroxyvitamin D3 supplementation on the hepatic microsomal and in vivo metabolism of vitamin D3 in vitamin D-depleted rats. J Clin Invest. 1986 Dec;78(6):1529–1537. doi: 10.1172/JCI112745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Haddad P., Gascon-Barré M., Dumont A. Comparative hepatic response to bromobenzene and allyl alcohol in the vitamin D-replete and vitamin D-depleted rat. J Pharmacol Exp Ther. 1985 May;233(2):499–506. [PubMed] [Google Scholar]
  19. Halloran B. P., Bikle D. D., Levens M. J., Castro M. E., Globus R. K., Holton E. Chronic 1,25-dihydroxyvitamin D3 administration in the rat reduces the serum concentration of 25-hydroxyvitamin D by increasing metabolic clearance rate. J Clin Invest. 1986 Sep;78(3):622–628. doi: 10.1172/JCI112619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Joseph S. K., Williamson J. R. The origin, quantitation, and kinetics of intracellular calcium mobilization by vasopressin and phenylephrine in hepatocytes. J Biol Chem. 1983 Sep 10;258(17):10425–10432. [PubMed] [Google Scholar]
  21. Madhok T. C., DeLuca H. F. Characteristics of the rat liver microsomal enzyme system converting cholecalciferol into 25-hydroxycholecalciferol. Evidence for the participation of cytochrome p-450. Biochem J. 1979 Dec 15;184(3):491–499. doi: 10.1042/bj1840491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Matsui I., Pegg A. E. Increase in acetylation of spermidine in rat liver extracts brought about by treatment with carbon tetrachloride. Biochem Biophys Res Commun. 1980 Feb 12;92(3):1009–1015. doi: 10.1016/0006-291x(80)90802-5. [DOI] [PubMed] [Google Scholar]
  23. Mawer E. B., Schaefer K., Lumb G. A., Stanbury S. W. The metabolism of isotopically labelled vitamin D3 in man: the influence of the state of vitamin D nutrition. Clin Sci. 1971 Jan;40(1):39–53. doi: 10.1042/cs0400039. [DOI] [PubMed] [Google Scholar]
  24. Milne M. L., Baran D. T. End product inhibition of hepatic 25-hydroxyvitamin D production in the rat: specificity and kinetics. Arch Biochem Biophys. 1985 Nov 1;242(2):488–492. doi: 10.1016/0003-9861(85)90234-6. [DOI] [PubMed] [Google Scholar]
  25. Nemere I., Yoshimoto Y., Norman A. W. Calcium transport in perfused duodena from normal chicks: enhancement within fourteen minutes of exposure to 1,25-dihydroxyvitamin D3. Endocrinology. 1984 Oct;115(4):1476–1483. doi: 10.1210/endo-115-4-1476. [DOI] [PubMed] [Google Scholar]
  26. Norman A. W., Ross F. P. Vitamin D seco-steroids: unique molecules with both hormone and possible membranophilic properties. Life Sci. 1979 Feb 26;24(9):759–769. doi: 10.1016/0024-3205(79)90359-x. [DOI] [PubMed] [Google Scholar]
  27. Reinhardt T. A., Horst R. L., Littledike E. T., Beitz D. C. 1,25-Dihydroxyvitamin D3 receptor in bovine thymus gland. Biochem Biophys Res Commun. 1982 Jun 15;106(3):1012–1018. doi: 10.1016/0006-291x(82)91812-5. [DOI] [PubMed] [Google Scholar]
  28. Sikorska M., Whitefield J. F., Rixon R. H. The effects of thyroparathyroidectomy and 1,25 dihydroxyvitamin D3 on changes in the activities of some cytoplasmic and nuclear protein kinases during liver regeneration. J Cell Physiol. 1983 Jun;115(3):297–304. doi: 10.1002/jcp.1041150313. [DOI] [PubMed] [Google Scholar]
  29. Youdale T., Whitfield J. F., Rixon R. H. 1 alpha,25-Dihydroxyvitamin D3 enables regenerating liver cells to make functional ribonucleotide reductase subunits and replicate DNA in thyroparathyroidectomized rats. Can J Biochem Cell Biol. 1985 May;63(5):319–324. doi: 10.1139/o85-047. [DOI] [PubMed] [Google Scholar]

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

RESOURCES