Literature DB >> 6546577

Calcitriol but no other metabolite of vitamin D is essential for normal bone growth and development in the rat.

A M Parfitt, C H Mathews, R Brommage, K Jarnagin, H F DeLuca.   

Abstract

To determine the relative importance of different metabolites of vitamin D in bone growth and development, weanling male rat pups suckled by vitamin D-deficient mothers were given either calcitriol (1,25-dihydroxycholecalciferol) by continuous subcutaneous infusion, oral calcidiol (25-hydroxycholecalciferol), or oral 24,24-difluoro-25-hydroxycholecalciferol, a synthetic compound that can undergo 1-hydroxylation but not 24-hydroxylation, as their sole source of vitamin D for 40 d. Pups raised in the same manner, but given no vitamin D, served as controls. The three metabolites compared were given in doses that restored normal plasma calcium levels and normal increments in body weight. After in vivo double tetracycline labeling, bone histomorphometry by standard methods was performed on one femur and one tail vertebra. There were no significant differences between the three metabolite-treated groups in length, periosteal or endosteal diameter, cortical cross-sectional area, cortical porosity, osteoid thickness and volume, appositional rate and bone formation rate in the femur, or in qualitative and quantitative indices of endochondral ossification in the tail vertebra. All three groups differed markedly from the untreated controls with respect to all measurements. Collectively, the data indicate that neither calcidiol nor any 24-hydroxylated metabolite of calcidiol is needed in the rat (other than as a precursor) for longitudinal or transverse bone growth, for normal endochondral ossification, or for normal periosteal and endosteal formation, mineralization, and resorption of bone. Calcitriol was fully active with respect to each of the indices listed when given in a manner resembling its continuous endogenous production by the kidney, suggesting that previous reports of incomplete skeletal response to calcitriol result from its rapid clearance and infrequent oral administration. We demonstrated that calcitriol is the only metabolite that is both necessary and sufficient for normal bone growth and development in the rat, but our data do not indicate the extent to which its beneficial skeletal effects were mediated by direct action on bone, either of calcitriol itself or of some metabolite thereof, or by restoration of normal plasma levels of calcium and phosphate.

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Year:  1984        PMID: 6546577      PMCID: PMC425051          DOI: 10.1172/JCI111246

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


  30 in total

1.  Lack of histological evidence of vitamin D abnormality in the bones of anephric patients.

Authors:  P J Bordier; S T Chot; J B Eastwood; A Fournier; H E de Wardener
Journal:  Clin Sci       Date:  1973-01       Impact factor: 6.124

2.  Formation, mineralization, and resorption of bone in vitamin D-deficient rats.

Authors:  D Baylink; M Stauffer; J Wergedal; C Rich
Journal:  J Clin Invest       Date:  1970-06       Impact factor: 14.808

3.  The action of vitamin D metabolites (25 OHD3--12,5 (OH)2D3--24.25 (OH)2D3--25.26 (OH)2D3) on vitamin D deficient rats.

Authors:  M L Queille; L Miravet; P Bordier; J Redel
Journal:  Biomedicine       Date:  1978 Jul-Aug

4.  24, 25-dihydroxyvitamin D is a metabolite of vitamin D essential for bone formation.

Authors:  A Ornoy; D Goodwin; D Noff; S Edelstein
Journal:  Nature       Date:  1978-11-30       Impact factor: 49.962

5.  Evidence for the metabolism of 24R-hydroxy-25-fluorovitamin D3 and 1alpha-hydroxy-25-fluorovitamin D3 to 1alpha,24R-dihydroxy-25-fluorovitamin D3.

Authors:  J L Napoli; W S Mellon; H K Schnoes; H F DeLuca
Journal:  Arch Biochem Biophys       Date:  1979-10-01       Impact factor: 4.013

6.  Biological activity of 24,24-difluoro-25-hydroxyvitamin D3. Effect of blocking of 24-hydroxylation on the functions of vitamin D.

Authors:  Y Tanaka; H F DeLuca; Y Kobayashi; T Taguchi; N Ikekawa; M Morisaki
Journal:  J Biol Chem       Date:  1979-08-10       Impact factor: 5.157

7.  Role of 1,25-dihydroxyvitamin D3 in maintaining serum phosphorus and curing rickets.

Authors:  Y Tanaka; H F Deluca
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

8.  Vitamin D metabolites and bone mineralization in man.

Authors:  P Bordier; H Rasmussen; P Marie; L Miravet; J Gueris; A Ryckwaert
Journal:  J Clin Endocrinol Metab       Date:  1978-02       Impact factor: 5.958

9.  Metabolism and binding properties of 24,24-difluoro-25-hydroxyvitamin D3.

Authors:  Y Tanaka; J K Wichmann; H F De Luca; Y Kobayashi; N Ikekawa
Journal:  Arch Biochem Biophys       Date:  1983-09       Impact factor: 4.013

10.  Normal plasma-1,25-(OH)2-vitamin-D concentrations in nutritional osteomalacia.

Authors:  J B Eastwood; H E de Wardener; R W Gray; J L Lemann
Journal:  Lancet       Date:  1979-06-30       Impact factor: 79.321

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  9 in total

1.  Indications on the use of vitamin D and vitamin D metabolites in clinical phenotypes.

Authors:  M L Brandi
Journal:  Clin Cases Miner Bone Metab       Date:  2010-09

Review 2.  Is 24,25(OH)D level really high in dialysis patients with high FGF23 levels?

Authors:  Hulya Taskapan
Journal:  Int Urol Nephrol       Date:  2012-03-31       Impact factor: 2.370

Review 3.  Use of calciferol and its metabolites and analogues in osteoporosis. Current status.

Authors:  A M Parfitt
Journal:  Drugs       Date:  1988-11       Impact factor: 9.546

Review 4.  Vitamin D: Metabolism, Molecular Mechanism of Action, and Pleiotropic Effects.

Authors:  Sylvia Christakos; Puneet Dhawan; Annemieke Verstuyf; Lieve Verlinden; Geert Carmeliet
Journal:  Physiol Rev       Date:  2016-01       Impact factor: 37.312

5.  Vitamin D metabolites prevent vertebral osteopenia in ovariectomized rats.

Authors:  R G Erben; H Weiser; F Sinowatz; W A Rambeck; H Zucker
Journal:  Calcif Tissue Int       Date:  1992-03       Impact factor: 4.333

6.  Enhancement of vitamin D metabolites in the eye following vitamin D3 supplementation and UV-B irradiation.

Authors:  Yanping Lin; John L Ubels; Mark P Schotanus; Zhaohong Yin; Victorina Pintea; Bruce D Hammock; Mitchell A Watsky
Journal:  Curr Eye Res       Date:  2012-05-25       Impact factor: 2.424

7.  Effect of 24R,25-dihydroxyvitamin D3 on the formation and function of osteoclastic cells.

Authors:  H Yamato; R Okazaki; T Ishii; E Ogata; T Sato; M Kumegawa; K Akaogi; N Taniguchi; T Matsumoto
Journal:  Calcif Tissue Int       Date:  1993-03       Impact factor: 4.333

8.  Increase of bone volume in vitamin D-repleted rats by massive administration of 24R,25(OH)2D3.

Authors:  T Nakamura; T Kurokawa; H Orimo
Journal:  Calcif Tissue Int       Date:  1988-10       Impact factor: 4.333

9.  The Vitamin D Metabolite Ratio Is Associated With Changes in Bone Density and Fracture Risk in Older Adults.

Authors:  Charles Ginsberg; Andrew N Hoofnagle; Ronit Katz; Jan Hughes-Austin; Lindsay M Miller; Jessica O Becker; Stephen B Kritchevsky; Michael G Shlipak; Mark J Sarnak; Joachim H Ix
Journal:  J Bone Miner Res       Date:  2021-08-29       Impact factor: 6.741

  9 in total

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