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High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats
BACKGROUND: The Dahl salt-sensitive rat, but not the Dahl salt-resistant rat, develops hypertension and hypovitaminosis D when fed a high salt diet. Since the salt-sensitive rat and salt-resistant rat were bred from the Sprague Dawley rat, the aim of this research was to test the hypothesis that sal...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018403/ https://www.ncbi.nlm.nih.gov/pubmed/21143930 http://dx.doi.org/10.1186/1756-0500-3-332 |
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author | Thierry-Palmer, Myrtle Tewolde, Teclemicael K Emmett, Neremiah L Bayorh, Mohamed A |
author_facet | Thierry-Palmer, Myrtle Tewolde, Teclemicael K Emmett, Neremiah L Bayorh, Mohamed A |
author_sort | Thierry-Palmer, Myrtle |
collection | PubMed |
description | BACKGROUND: The Dahl salt-sensitive rat, but not the Dahl salt-resistant rat, develops hypertension and hypovitaminosis D when fed a high salt diet. Since the salt-sensitive rat and salt-resistant rat were bred from the Sprague Dawley rat, the aim of this research was to test the hypothesis that salt-resistant and Sprague Dawley rats would be similar in their vitamin D endocrine system response to high salt intake. FINDINGS: Sprague Dawley, salt-sensitive, and salt-resistant rats were fed high (80 g/kg, 8%) or low (3 g/kg, 3%) salt diets for three weeks. The blood pressure of Sprague Dawley rats increased from baseline to week 3 during both high and low salt intake and the mean blood pressure at week 3 of high salt intake was higher than that at week 3 of low salt intake (P < 0.05). Mean plasma 25-hydroxyvitamin D concentrations (marker of vitamin D status) of Sprague Dawley, salt-sensitive, and salt-resistant rats were similar at week 3 of low salt intake. Mean plasma 25-hydroxyvitamin D concentrations of Sprague Dawley and salt-resistant rats were unaffected by high salt intake, whereas the mean plasma 25-hydroxyvitamin D concentration of salt-sensitive rats at week 3 of high salt intake was only 20% of that at week 3 of low salt intake. CONCLUSIONS: These data indicate that the effect of high salt intake on the vitamin D endocrine system of Sprague Dawley rats at week 3 was similar to that of salt-resistant rats. The salt-sensitive rat, thus, appears to be a more appropriate model than the Sprague Dawley rat for assessing possible effects of salt-sensitivity on vitamin D status of humans. |
format | Text |
id | pubmed-3018403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30184032011-01-11 High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats Thierry-Palmer, Myrtle Tewolde, Teclemicael K Emmett, Neremiah L Bayorh, Mohamed A BMC Res Notes Short Report BACKGROUND: The Dahl salt-sensitive rat, but not the Dahl salt-resistant rat, develops hypertension and hypovitaminosis D when fed a high salt diet. Since the salt-sensitive rat and salt-resistant rat were bred from the Sprague Dawley rat, the aim of this research was to test the hypothesis that salt-resistant and Sprague Dawley rats would be similar in their vitamin D endocrine system response to high salt intake. FINDINGS: Sprague Dawley, salt-sensitive, and salt-resistant rats were fed high (80 g/kg, 8%) or low (3 g/kg, 3%) salt diets for three weeks. The blood pressure of Sprague Dawley rats increased from baseline to week 3 during both high and low salt intake and the mean blood pressure at week 3 of high salt intake was higher than that at week 3 of low salt intake (P < 0.05). Mean plasma 25-hydroxyvitamin D concentrations (marker of vitamin D status) of Sprague Dawley, salt-sensitive, and salt-resistant rats were similar at week 3 of low salt intake. Mean plasma 25-hydroxyvitamin D concentrations of Sprague Dawley and salt-resistant rats were unaffected by high salt intake, whereas the mean plasma 25-hydroxyvitamin D concentration of salt-sensitive rats at week 3 of high salt intake was only 20% of that at week 3 of low salt intake. CONCLUSIONS: These data indicate that the effect of high salt intake on the vitamin D endocrine system of Sprague Dawley rats at week 3 was similar to that of salt-resistant rats. The salt-sensitive rat, thus, appears to be a more appropriate model than the Sprague Dawley rat for assessing possible effects of salt-sensitivity on vitamin D status of humans. BioMed Central 2010-12-09 /pmc/articles/PMC3018403/ /pubmed/21143930 http://dx.doi.org/10.1186/1756-0500-3-332 Text en Copyright ©2010 Thierry-Palmer et al; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Thierry-Palmer, Myrtle Tewolde, Teclemicael K Emmett, Neremiah L Bayorh, Mohamed A High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats |
title | High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats |
title_full | High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats |
title_fullStr | High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats |
title_full_unstemmed | High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats |
title_short | High dietary salt does not significantly affect plasma 25-hydroxyvitamin D concentrations of Sprague Dawley rats |
title_sort | high dietary salt does not significantly affect plasma 25-hydroxyvitamin d concentrations of sprague dawley rats |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018403/ https://www.ncbi.nlm.nih.gov/pubmed/21143930 http://dx.doi.org/10.1186/1756-0500-3-332 |
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