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Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney

There is evidence that dietary fats are important components contributing in bone health and that bone mineral density is inversely related to sodium intake. Salt loading is also known to impose negative effects on renal function. The present study aimed to determine the effect of the polyunsaturate...

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Autores principales: Ahmed, Mona A, Abd EL Samad, Abeer A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841042/
https://www.ncbi.nlm.nih.gov/pubmed/24303178
http://dx.doi.org/10.1002/phy2.106
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author Ahmed, Mona A
Abd EL Samad, Abeer A
author_facet Ahmed, Mona A
Abd EL Samad, Abeer A
author_sort Ahmed, Mona A
collection PubMed
description There is evidence that dietary fats are important components contributing in bone health and that bone mineral density is inversely related to sodium intake. Salt loading is also known to impose negative effects on renal function. The present study aimed to determine the effect of the polyunsaturated fatty acid omega-3 on bone changes imposed by salt loading, highlighting the role of kidney as a potential mechanism involved in this effect. Male Wistar rats were divided into three groups: control group, salt-loaded group consuming 2% NaCl solution as drinking water for 8 weeks, and omega-3-treated salt-loaded group receiving 1 g/kg/day omega-3 by gavage with consumption of 2% NaCl solution for 8 weeks. Systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP), and heart rate (HR) were recorded. Plasma levels of sodium, potassium, calcium, inorganic phosphorus (Pi), alkaline phosphatase (ALP), creatinine, urea, 1,25-dihydroxyvitamin D [1,25(OH)(2)D(3)], and transforming growth factor-beta1 (TGF-β1) were measured. The right tibia and kidney were removed for histologic examination and renal immunohistochemical analysis for endothelial nitric oxide synthase (eNOS) was performed. The results revealed that omega-3 reduced SBP, DBP, and MAP and plasma levels of sodium, potassium, Pi, creatinine, urea, and TGF-β1, but increased plasma levels of calcium, ALP, and 1,25(OH)(2)D(3) as well as renal eNOS. Omega-3 increased cortical and trabecular bone thickness, decreased osteoclast number, and increased newly formed osteoid bone. Renal morphology was found preserved. In conclusion, omega-3 prevents the disturbed bone status imposed by salt loading. This osteoprotective effect is possibly mediated by attenuation of alterations in Ca(2+), Pi, and ALP, and improvement of renal function and arterial blood pressure.
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spelling pubmed-38410422013-12-03 Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney Ahmed, Mona A Abd EL Samad, Abeer A Physiol Rep Original Research There is evidence that dietary fats are important components contributing in bone health and that bone mineral density is inversely related to sodium intake. Salt loading is also known to impose negative effects on renal function. The present study aimed to determine the effect of the polyunsaturated fatty acid omega-3 on bone changes imposed by salt loading, highlighting the role of kidney as a potential mechanism involved in this effect. Male Wistar rats were divided into three groups: control group, salt-loaded group consuming 2% NaCl solution as drinking water for 8 weeks, and omega-3-treated salt-loaded group receiving 1 g/kg/day omega-3 by gavage with consumption of 2% NaCl solution for 8 weeks. Systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP), and heart rate (HR) were recorded. Plasma levels of sodium, potassium, calcium, inorganic phosphorus (Pi), alkaline phosphatase (ALP), creatinine, urea, 1,25-dihydroxyvitamin D [1,25(OH)(2)D(3)], and transforming growth factor-beta1 (TGF-β1) were measured. The right tibia and kidney were removed for histologic examination and renal immunohistochemical analysis for endothelial nitric oxide synthase (eNOS) was performed. The results revealed that omega-3 reduced SBP, DBP, and MAP and plasma levels of sodium, potassium, Pi, creatinine, urea, and TGF-β1, but increased plasma levels of calcium, ALP, and 1,25(OH)(2)D(3) as well as renal eNOS. Omega-3 increased cortical and trabecular bone thickness, decreased osteoclast number, and increased newly formed osteoid bone. Renal morphology was found preserved. In conclusion, omega-3 prevents the disturbed bone status imposed by salt loading. This osteoprotective effect is possibly mediated by attenuation of alterations in Ca(2+), Pi, and ALP, and improvement of renal function and arterial blood pressure. Blackwell Publishing Ltd 2013-10 2013-09-23 /pmc/articles/PMC3841042/ /pubmed/24303178 http://dx.doi.org/10.1002/phy2.106 Text en © 2013 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Research
Ahmed, Mona A
Abd EL Samad, Abeer A
Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
title Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
title_full Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
title_fullStr Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
title_full_unstemmed Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
title_short Benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
title_sort benefits of omega-3 fatty acid against bone changes in salt-loaded rats: possible role of kidney
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841042/
https://www.ncbi.nlm.nih.gov/pubmed/24303178
http://dx.doi.org/10.1002/phy2.106
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