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The effects of intramuscularly administered vitamin D3, 25- and 1 alpha-hydroxycholecalciferol in cows on plasma mineral content, plasma 25-hydroxycholecalciferol and on mineral deposits in soft tissues.

Abstract
The investigations were carried out to evaluate potential side effects of a prophylaxis with high doses of vitamin D3 and vitamin D metabolites in parturient paresis. For this reason, 10(7) IU vitamin D3 (= 250 mg), 4 mg 25-OHD3 or 420 micrograms 1 alpha-OHD3 were applied to non-gravid dairy cows at the end of lactation. The application was repeated 3 times at one week intervals and the changes of the mineral concentration and 25-OHD were measured in the plasma. The pathomorphological changes in the cardio-vascular system and other organs were examined macro- and microscopically. The application of vitamin D3 and 25-OHD3 led to an immediate and continuous increase of the 25-OHD concentration in the plasma. On the other hand, administration of 1 alpha-OHD3 resulted in a decrease of the 25-OHD level. After the application of vitamin D3 and 1 alpha-OHD3, the Ca and Pi concentration increased significantly. After 25-OHD3, the Ca concentration decreased below the initial level in the second week. The administration of all 3 compounds led to a significant decrease of the Mg concentration after the first injection. The administration of vitamin D3 and 1 alpha-OHD3 resulted in a significantly more pronounced calcinosis of inner organs while after the application of 25-OHD3 only occasionally calcium deposits were observed in the vascular system.
AuthorsH Zepperitz, G Jahreis, H Kiupel, V Hesse
JournalZentralblatt fur Veterinarmedizin. Reihe A (Zentralbl Veterinarmed A) Vol. 38 Issue 10 Pg. 763-9 (Dec 1991) ISSN: 0514-7158 [Print] Germany
PMID1665630 (Publication Type: Journal Article)
Chemical References
  • Hydroxycholecalciferols
  • Minerals
  • Cholecalciferol
  • Calcifediol
  • alfacalcidol
Topics
  • Animals
  • Calcifediol (blood, pharmacology)
  • Cattle (metabolism)
  • Cholecalciferol (pharmacology)
  • Female
  • Hydroxycholecalciferols (pharmacology)
  • Minerals (blood, metabolism)

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