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Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats
PURPOSE: Hydroxocobalamin (HOCbl) is the dominating Cbl form in food, whereas cyanocobalamin (CNCbl) is common in vitamin pills and oral supplements. This study compares single-dose absorption and distribution of oral HO[(57)Co]Cbl and CN[(57)Co]Cbl in Cbl-deficient and normal rats. METHODS: Male Wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960002/ https://www.ncbi.nlm.nih.gov/pubmed/28321545 http://dx.doi.org/10.1007/s00394-017-1424-0 |
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author | Kornerup, Linda S. Fedosov, Sergey N. Juul, Christian B. Greibe, Eva Heegaard, Christian W. Nexo, Ebba |
author_facet | Kornerup, Linda S. Fedosov, Sergey N. Juul, Christian B. Greibe, Eva Heegaard, Christian W. Nexo, Ebba |
author_sort | Kornerup, Linda S. |
collection | PubMed |
description | PURPOSE: Hydroxocobalamin (HOCbl) is the dominating Cbl form in food, whereas cyanocobalamin (CNCbl) is common in vitamin pills and oral supplements. This study compares single-dose absorption and distribution of oral HO[(57)Co]Cbl and CN[(57)Co]Cbl in Cbl-deficient and normal rats. METHODS: Male Wistar rats (7 weeks) were fed a 14-day diet with (n = 15) or without (n = 15) Cbl. We compared the uptakes of HO[(57)Co]Cbl (free or bound to bovine transcobalamin) and free CN[(57)Co]Cbl administered by gastric gavage (n = 5 in each diet group). Rats were sacrificed after 24 h. Blood, liver, kidney, brain, heart, spleen, intestines, skeletal muscle, 24-h urine and faeces were collected, and the content of [(57)Co]Cbl was measured. Endogenous Cbl in tissues and plasma was analysed by routine methods. RESULTS: Mean endogenous plasma-Cbl was sevenfold lower in deficient vs. normal rats (190 vs. 1330 pmol/L, p < 0.0001). Cbl depletion increased endogenous Cbl ratios (tissue/plasma = k (in)/k (out)) in all organs except for the kidney, where the ratio decreased considerably. Twenty-four-hour accumulation of labelled Cbl showed that HOCbl > CNCbl (liver) and CNCbl > HOCbl (brain, muscle and plasma). CONCLUSIONS: The Cbl status of rats and the administered Cbl form influence 24-h Cbl accumulation in tissues and plasma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-017-1424-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5960002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-59600022018-05-24 Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats Kornerup, Linda S. Fedosov, Sergey N. Juul, Christian B. Greibe, Eva Heegaard, Christian W. Nexo, Ebba Eur J Nutr Original Contribution PURPOSE: Hydroxocobalamin (HOCbl) is the dominating Cbl form in food, whereas cyanocobalamin (CNCbl) is common in vitamin pills and oral supplements. This study compares single-dose absorption and distribution of oral HO[(57)Co]Cbl and CN[(57)Co]Cbl in Cbl-deficient and normal rats. METHODS: Male Wistar rats (7 weeks) were fed a 14-day diet with (n = 15) or without (n = 15) Cbl. We compared the uptakes of HO[(57)Co]Cbl (free or bound to bovine transcobalamin) and free CN[(57)Co]Cbl administered by gastric gavage (n = 5 in each diet group). Rats were sacrificed after 24 h. Blood, liver, kidney, brain, heart, spleen, intestines, skeletal muscle, 24-h urine and faeces were collected, and the content of [(57)Co]Cbl was measured. Endogenous Cbl in tissues and plasma was analysed by routine methods. RESULTS: Mean endogenous plasma-Cbl was sevenfold lower in deficient vs. normal rats (190 vs. 1330 pmol/L, p < 0.0001). Cbl depletion increased endogenous Cbl ratios (tissue/plasma = k (in)/k (out)) in all organs except for the kidney, where the ratio decreased considerably. Twenty-four-hour accumulation of labelled Cbl showed that HOCbl > CNCbl (liver) and CNCbl > HOCbl (brain, muscle and plasma). CONCLUSIONS: The Cbl status of rats and the administered Cbl form influence 24-h Cbl accumulation in tissues and plasma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-017-1424-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-03-20 2018 /pmc/articles/PMC5960002/ /pubmed/28321545 http://dx.doi.org/10.1007/s00394-017-1424-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Contribution Kornerup, Linda S. Fedosov, Sergey N. Juul, Christian B. Greibe, Eva Heegaard, Christian W. Nexo, Ebba Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats |
title | Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats |
title_full | Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats |
title_fullStr | Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats |
title_full_unstemmed | Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats |
title_short | Tissue distribution of oral vitamin B12 is influenced by B12 status and B12 form: an experimental study in rats |
title_sort | tissue distribution of oral vitamin b12 is influenced by b12 status and b12 form: an experimental study in rats |
topic | Original Contribution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960002/ https://www.ncbi.nlm.nih.gov/pubmed/28321545 http://dx.doi.org/10.1007/s00394-017-1424-0 |
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