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Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation
BACKGROUND & OBJECTIVES: Iron supplementation is usually given to pregnant and lactating women who may also have marginal deficiency of zinc. The negative impact of supplemental iron and calcium on zinc status is a cause of concern. The present investigation was undertaken to examine the effect...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859134/ https://www.ncbi.nlm.nih.gov/pubmed/27121523 http://dx.doi.org/10.4103/0971-5916.180221 |
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author | Jayalakshmi, S. Platel, Kalpana |
author_facet | Jayalakshmi, S. Platel, Kalpana |
author_sort | Jayalakshmi, S. |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: Iron supplementation is usually given to pregnant and lactating women who may also have marginal deficiency of zinc. The negative impact of supplemental iron and calcium on zinc status is a cause of concern. The present investigation was undertaken to examine the effect of inclusion of iron and calcium in the diet at supplementary levels on zinc status of experimental rats. METHODS: Groups of experimental rats were maintained on diets supplemented with iron (Molar ratio - Zn:Fe 1:30) and calcium (Molar ratio - Zn:Ca 1:667) both individually and in combination for six weeks. Zinc status of these rats was assessed by determining zinc concentration in circulation and in organs, and the activities of zinc containing enzymes in serum and liver. RESULTS: The zinc status of experimental rats receiving supplemental levels of iron and calcium was significantly compromised. Zinc concentration in serum, kidney, spleen and liver was reduced significantly by both these minerals. Six weeks of supplementation of iron and calcium individually, significantly reduced the activity of liver and serum superoxide dismutase and alkaline phosphatase. Activity of liver alcohol dehydrogenase was lowered in calcium supplemented group and in calcium + iron supplemented group, while that of carbonic anhydrase was significantly reduced by iron, calcium and their combination. INTERPRETATION & CONCLUSIONS: Supplemental levels of iron and calcium, both individually and in combination, significantly compromised the zinc status of experimental rats. This negative effect of these two minerals was more prominent when these were supplemented for a period of six weeks. |
format | Online Article Text |
id | pubmed-4859134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48591342016-05-16 Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation Jayalakshmi, S. Platel, Kalpana Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Iron supplementation is usually given to pregnant and lactating women who may also have marginal deficiency of zinc. The negative impact of supplemental iron and calcium on zinc status is a cause of concern. The present investigation was undertaken to examine the effect of inclusion of iron and calcium in the diet at supplementary levels on zinc status of experimental rats. METHODS: Groups of experimental rats were maintained on diets supplemented with iron (Molar ratio - Zn:Fe 1:30) and calcium (Molar ratio - Zn:Ca 1:667) both individually and in combination for six weeks. Zinc status of these rats was assessed by determining zinc concentration in circulation and in organs, and the activities of zinc containing enzymes in serum and liver. RESULTS: The zinc status of experimental rats receiving supplemental levels of iron and calcium was significantly compromised. Zinc concentration in serum, kidney, spleen and liver was reduced significantly by both these minerals. Six weeks of supplementation of iron and calcium individually, significantly reduced the activity of liver and serum superoxide dismutase and alkaline phosphatase. Activity of liver alcohol dehydrogenase was lowered in calcium supplemented group and in calcium + iron supplemented group, while that of carbonic anhydrase was significantly reduced by iron, calcium and their combination. INTERPRETATION & CONCLUSIONS: Supplemental levels of iron and calcium, both individually and in combination, significantly compromised the zinc status of experimental rats. This negative effect of these two minerals was more prominent when these were supplemented for a period of six weeks. Medknow Publications & Media Pvt Ltd 2016-02 /pmc/articles/PMC4859134/ /pubmed/27121523 http://dx.doi.org/10.4103/0971-5916.180221 Text en Copyright: © Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Jayalakshmi, S. Platel, Kalpana Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
title | Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
title_full | Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
title_fullStr | Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
title_full_unstemmed | Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
title_short | Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
title_sort | compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859134/ https://www.ncbi.nlm.nih.gov/pubmed/27121523 http://dx.doi.org/10.4103/0971-5916.180221 |
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