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Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis
The purpose of this study was to induce experimental periodontitis in rats previously fed diets containing arginine silicate inositol (ASI) complex and examine the biochemical, immunological, and radiological effects. Fifty two 8-week-old female Sprague Dawley rats were equally divided into four gro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117900/ https://www.ncbi.nlm.nih.gov/pubmed/27895467 http://dx.doi.org/10.2147/DDDT.S115088 |
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author | Dundar, Serkan Eltas, Abubekir Hakki, Sema S Malkoc, Sıddık Uslu, M Ozay Tuzcu, Mehmet Komorowski, James Ozercan, I Hanifi Akdemir, Fatih Sahin, Kazim |
author_facet | Dundar, Serkan Eltas, Abubekir Hakki, Sema S Malkoc, Sıddık Uslu, M Ozay Tuzcu, Mehmet Komorowski, James Ozercan, I Hanifi Akdemir, Fatih Sahin, Kazim |
author_sort | Dundar, Serkan |
collection | PubMed |
description | The purpose of this study was to induce experimental periodontitis in rats previously fed diets containing arginine silicate inositol (ASI) complex and examine the biochemical, immunological, and radiological effects. Fifty two 8-week-old female Sprague Dawley rats were equally divided into four groups. The control group included those fed a standard rat diet with no operation performed during the experiment. The periodontitis, ASI I, and ASI II groups were subjected to experimental periodontitis induction for 11 days after being fed a standard rat diet alone, a diet containing 1.81 g/kg ASI complex, or a diet containing 3.62 g/kg ASI complex, respectively, for 8 weeks. Throughout the 11-day duration of periodontitis induction, all rats were fed standard feed. The rats were euthanized on the eleventh day, and their tissue and blood samples were collected. In the periodontitis group, elevated tissue destruction parameters and reduced tissue formation parameters were found, as compared to the ASI groups. Levels of enzymes, cytokines, and mediators associated with periodontal tissue destruction were lower in rats fed a diet containing ASI complex after experimental periodontitis. These results indicate that ASI complex could be an alternative agent for host modulation. |
format | Online Article Text |
id | pubmed-5117900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51179002016-11-28 Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis Dundar, Serkan Eltas, Abubekir Hakki, Sema S Malkoc, Sıddık Uslu, M Ozay Tuzcu, Mehmet Komorowski, James Ozercan, I Hanifi Akdemir, Fatih Sahin, Kazim Drug Des Devel Ther Original Research The purpose of this study was to induce experimental periodontitis in rats previously fed diets containing arginine silicate inositol (ASI) complex and examine the biochemical, immunological, and radiological effects. Fifty two 8-week-old female Sprague Dawley rats were equally divided into four groups. The control group included those fed a standard rat diet with no operation performed during the experiment. The periodontitis, ASI I, and ASI II groups were subjected to experimental periodontitis induction for 11 days after being fed a standard rat diet alone, a diet containing 1.81 g/kg ASI complex, or a diet containing 3.62 g/kg ASI complex, respectively, for 8 weeks. Throughout the 11-day duration of periodontitis induction, all rats were fed standard feed. The rats were euthanized on the eleventh day, and their tissue and blood samples were collected. In the periodontitis group, elevated tissue destruction parameters and reduced tissue formation parameters were found, as compared to the ASI groups. Levels of enzymes, cytokines, and mediators associated with periodontal tissue destruction were lower in rats fed a diet containing ASI complex after experimental periodontitis. These results indicate that ASI complex could be an alternative agent for host modulation. Dove Medical Press 2016-11-15 /pmc/articles/PMC5117900/ /pubmed/27895467 http://dx.doi.org/10.2147/DDDT.S115088 Text en © 2016 Dundar et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Dundar, Serkan Eltas, Abubekir Hakki, Sema S Malkoc, Sıddık Uslu, M Ozay Tuzcu, Mehmet Komorowski, James Ozercan, I Hanifi Akdemir, Fatih Sahin, Kazim Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
title | Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
title_full | Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
title_fullStr | Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
title_full_unstemmed | Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
title_short | Dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
title_sort | dietary arginine silicate inositol complex inhibits periodontal tissue loss in rats with ligature-induced periodontitis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117900/ https://www.ncbi.nlm.nih.gov/pubmed/27895467 http://dx.doi.org/10.2147/DDDT.S115088 |
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