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Resveratrol inhibits the intracellular calcium increase and angiotensin/endothelin system activation induced by soluble uric acid in mesangial cells
Resveratrol (Resv) is natural polyphenol found in grapes. This study evaluated the protective effect of Resv against the effects of uric acid (UA) in immortalized human mesangial cells (ihMCs). ihMCs were preincubated with Resv (12.5 µM) for 1 h and treated with UA (10 mg/dL) for 6 or 12 h. The intr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Associação Brasileira de Divulgação Científica
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288493/ https://www.ncbi.nlm.nih.gov/pubmed/25493383 http://dx.doi.org/10.1590/1414-431X20144032 |
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author | Albertoni, G. Schor, N. |
author_facet | Albertoni, G. Schor, N. |
author_sort | Albertoni, G. |
collection | PubMed |
description | Resveratrol (Resv) is natural polyphenol found in grapes. This study evaluated the protective effect of Resv against the effects of uric acid (UA) in immortalized human mesangial cells (ihMCs). ihMCs were preincubated with Resv (12.5 µM) for 1 h and treated with UA (10 mg/dL) for 6 or 12 h. The intracellular calcium concentration [Ca(2+)]i was quantified by fluorescence using flow cytometry. Angiotensinogen (AGT) and pre-pro endothelin-1 (ppET-1) mRNA were assayed by quantitative real-time RT-PCR. Angiotensin II (AII) and endothelin-1 (ET-1) were assayed by ELISA. UA significantly increased [Ca(2+)]i. Pre-incubation with Resv significantly reduced the change in [Ca(2+)]i induced by UA. Incubation with UA for 6 or 12 h also increased AGT mRNA expression and AII protein synthesis. Resv blunted these increases in AGT mRNA expression and AII protein. Incubation with UA in the ihMCs increased ppET-1 expression and ET-1 protein synthesis at 6 and 12 h. When ihMCs were pre-incubated with Resv, UA had a significantly diminished effect on ppET-1 mRNA expression and ET-1 protein synthesis at 6 and 12 h, respectively. Our results suggested that UA triggers reactions including AII and ET-1 production in mesangial cells. The renin-angiotensin system may contribute to the pathogenesis of renal function and chronic kidney disease. Resv can minimize the impact of UA on AII, ET-1 and the increase of [Ca(2+)]i in mesangial cells, suggesting that, at least in part, Resv can prevent the effects of soluble UA in mesangial cells. |
format | Online Article Text |
id | pubmed-4288493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-42884932015-01-21 Resveratrol inhibits the intracellular calcium increase and angiotensin/endothelin system activation induced by soluble uric acid in mesangial cells Albertoni, G. Schor, N. Braz J Med Biol Res Biomedical Sciences Resveratrol (Resv) is natural polyphenol found in grapes. This study evaluated the protective effect of Resv against the effects of uric acid (UA) in immortalized human mesangial cells (ihMCs). ihMCs were preincubated with Resv (12.5 µM) for 1 h and treated with UA (10 mg/dL) for 6 or 12 h. The intracellular calcium concentration [Ca(2+)]i was quantified by fluorescence using flow cytometry. Angiotensinogen (AGT) and pre-pro endothelin-1 (ppET-1) mRNA were assayed by quantitative real-time RT-PCR. Angiotensin II (AII) and endothelin-1 (ET-1) were assayed by ELISA. UA significantly increased [Ca(2+)]i. Pre-incubation with Resv significantly reduced the change in [Ca(2+)]i induced by UA. Incubation with UA for 6 or 12 h also increased AGT mRNA expression and AII protein synthesis. Resv blunted these increases in AGT mRNA expression and AII protein. Incubation with UA in the ihMCs increased ppET-1 expression and ET-1 protein synthesis at 6 and 12 h. When ihMCs were pre-incubated with Resv, UA had a significantly diminished effect on ppET-1 mRNA expression and ET-1 protein synthesis at 6 and 12 h, respectively. Our results suggested that UA triggers reactions including AII and ET-1 production in mesangial cells. The renin-angiotensin system may contribute to the pathogenesis of renal function and chronic kidney disease. Resv can minimize the impact of UA on AII, ET-1 and the increase of [Ca(2+)]i in mesangial cells, suggesting that, at least in part, Resv can prevent the effects of soluble UA in mesangial cells. Associação Brasileira de Divulgação Científica 2014-10-24 /pmc/articles/PMC4288493/ /pubmed/25493383 http://dx.doi.org/10.1590/1414-431X20144032 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedical Sciences Albertoni, G. Schor, N. Resveratrol inhibits the intracellular calcium increase and angiotensin/endothelin system activation induced by soluble uric acid in mesangial cells |
title | Resveratrol inhibits the intracellular calcium increase and
angiotensin/endothelin system activation induced by soluble uric acid in mesangial
cells |
title_full | Resveratrol inhibits the intracellular calcium increase and
angiotensin/endothelin system activation induced by soluble uric acid in mesangial
cells |
title_fullStr | Resveratrol inhibits the intracellular calcium increase and
angiotensin/endothelin system activation induced by soluble uric acid in mesangial
cells |
title_full_unstemmed | Resveratrol inhibits the intracellular calcium increase and
angiotensin/endothelin system activation induced by soluble uric acid in mesangial
cells |
title_short | Resveratrol inhibits the intracellular calcium increase and
angiotensin/endothelin system activation induced by soluble uric acid in mesangial
cells |
title_sort | resveratrol inhibits the intracellular calcium increase and
angiotensin/endothelin system activation induced by soluble uric acid in mesangial
cells |
topic | Biomedical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288493/ https://www.ncbi.nlm.nih.gov/pubmed/25493383 http://dx.doi.org/10.1590/1414-431X20144032 |
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