No difference in intestinal strontium absorption after an oral or an intravenous 1,25(OH)2D3 bolus in normal subjects

It has been suggested that 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) stimulates intestinal calcium absorption less via the intravenous (iv) than the oral route, because the first avoids direct contact of the drug with the enterocytes. However, no study has addressed the issue directly. This investigati...

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Hauptverfasser: Bianchi, Maria L. (VerfasserIn) , Ardissino, Gianluigi (VerfasserIn) , Schmitt, Claus P. (VerfasserIn) , Daccó, V. (VerfasserIn) , Barletta, L. (VerfasserIn) , Claris‐Appiani, A. (VerfasserIn) , Mehls, Otto (VerfasserIn)
Körperschaft: European Study Group on Vitamin D in Children with Renal Failure (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1999
In: Journal of bone and mineral research
Year: 1999, Jahrgang: 14, Heft: 10, Pages: 1789-1795
ISSN:1523-4681
DOI:https://doi.org/10.1359/jbmr.1999.14.10.1789
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1359/jbmr.1999.14.10.1789
Verlag, lizenzpflichtig, Volltext: https://asbmr.onlinelibrary.wiley.com/doi/abs/10.1359/jbmr.1999.14.10.1789
Volltext
Verfasserangaben:M.L. Bianchi, G.L. Ardissino, C.P. Schmitt, V. Daccó, L. Barletta, A. Claris‐Appiani, O. Mehls for the European Study Group on Vitamin D in Children with Renal Failure

MARC

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245 1 0 |a No difference in intestinal strontium absorption after an oral or an intravenous 1,25(OH)2D3 bolus in normal subjects  |c M.L. Bianchi, G.L. Ardissino, C.P. Schmitt, V. Daccó, L. Barletta, A. Claris‐Appiani, O. Mehls for the European Study Group on Vitamin D in Children with Renal Failure 
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500 |a First published: 02 December 2009 
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520 |a It has been suggested that 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) stimulates intestinal calcium absorption less via the intravenous (iv) than the oral route, because the first avoids direct contact of the drug with the enterocytes. However, no study has addressed the issue directly. This investigation was designed to measure the effect of a single oral or iv dose of 1,25(OH)2D3 on calcium absorption, using stable strontium (Sr) as a surrogate for calcium, and measuring the Sr fractional absorbed dose (FAD%) over 240 minutes after Sr administration. In 10 healthy volunteers, five tests were performed in a cross-over design, with a wash-out period between two consecutive tests: Sr absorption without 1,25(OH)2D3 (test A); Sr absorption immediately after either oral (test B) or iv (test C) 1,25(OH)2D3 (1.5 μg/m2 of body surface area [BSA]); Sr absorption (24 hr after either oral (test D) or iv (test E) 1,25(OH)2D3 (1.5 μg/m2 BSA). The concurrent administration of 1,25(OH)2D3 and Sr (tests B and C) did not significantly change the area under the Sr FAD%-time curve with respect to test A (test A: 4090 ± 345; test B: 4510 ± 345; test C: 4210 ± 345), whereas Sr absorption was significantly increased (p < 0.001) when Sr was given 24 hr after either oral or iv 1,25(OH)2D3 (test D: 5710 ± 345; test E: 5510 ± 345). It was concluded that 1,25(OH)2D3 is likely to influence calcium absorption significantly only via its genomic effect, independent of its administration route. 
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