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Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study

BACKGROUND: Arginine silicate inositol complex (ASI; arginine 49.5%, silicon 8.2%, and inositol 25%) is a novel material that is a bioavailable source of silicon and arginine. ASI offers potential benefits for vascular and bone health. OBJECTIVE: The aim of this study was to evaluate the potential e...

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Autores principales: Yaman, Ferhan, Acikan, Izzet, Dundar, Serkan, Simsek, Sercan, Gul, Mehmet, Ozercan, Ibrahim Hanifi, Komorowski, James, Sahin, Kazim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930222/
https://www.ncbi.nlm.nih.gov/pubmed/27390517
http://dx.doi.org/10.2147/DDDT.S109271
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author Yaman, Ferhan
Acikan, Izzet
Dundar, Serkan
Simsek, Sercan
Gul, Mehmet
Ozercan, Ibrahim Hanifi
Komorowski, James
Sahin, Kazim
author_facet Yaman, Ferhan
Acikan, Izzet
Dundar, Serkan
Simsek, Sercan
Gul, Mehmet
Ozercan, Ibrahim Hanifi
Komorowski, James
Sahin, Kazim
author_sort Yaman, Ferhan
collection PubMed
description BACKGROUND: Arginine silicate inositol complex (ASI; arginine 49.5%, silicon 8.2%, and inositol 25%) is a novel material that is a bioavailable source of silicon and arginine. ASI offers potential benefits for vascular and bone health. OBJECTIVE: The aim of this study was to evaluate the potential effects of ASI complex on bone healing of critical-sized defects in rats. METHODS: The rats were randomly assigned to two groups of 21 rats each. The control group was fed a standard diet for 12 weeks; after the first 8 weeks, a calvarial critical-sized defect was created, and the rats were sacrificed 7, 14, and 28 days later. The ASI group was fed a diet containing 1.81 g/kg of ASI for 12 weeks; after the first 8 weeks, a calvarial critical-sized defect was created, and the rats were sacrificed 7, 14, and 28 days later. The calvarial bones of all the rats were then harvested for evaluation. RESULTS: Osteoblasts and osteoclasts were detected at higher levels in the ASI group compared with the control group at days 7, 14, and 28 of the calvarial defect (P<0.05). New bone formation was detected at higher levels in the ASI group compared with the controls at day 28 (P<0.05). However, new bone formation was not detected at days 7 and 14 in both the groups (P>0.05). CONCLUSION: ASI supplementation significantly improved bone tissue healing in rats with critical-sized defects. This study demonstrated that ASI can enhance bone repair and has potential as a therapeutic regimen in humans.
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spelling pubmed-49302222016-07-07 Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study Yaman, Ferhan Acikan, Izzet Dundar, Serkan Simsek, Sercan Gul, Mehmet Ozercan, Ibrahim Hanifi Komorowski, James Sahin, Kazim Drug Des Devel Ther Original Research BACKGROUND: Arginine silicate inositol complex (ASI; arginine 49.5%, silicon 8.2%, and inositol 25%) is a novel material that is a bioavailable source of silicon and arginine. ASI offers potential benefits for vascular and bone health. OBJECTIVE: The aim of this study was to evaluate the potential effects of ASI complex on bone healing of critical-sized defects in rats. METHODS: The rats were randomly assigned to two groups of 21 rats each. The control group was fed a standard diet for 12 weeks; after the first 8 weeks, a calvarial critical-sized defect was created, and the rats were sacrificed 7, 14, and 28 days later. The ASI group was fed a diet containing 1.81 g/kg of ASI for 12 weeks; after the first 8 weeks, a calvarial critical-sized defect was created, and the rats were sacrificed 7, 14, and 28 days later. The calvarial bones of all the rats were then harvested for evaluation. RESULTS: Osteoblasts and osteoclasts were detected at higher levels in the ASI group compared with the control group at days 7, 14, and 28 of the calvarial defect (P<0.05). New bone formation was detected at higher levels in the ASI group compared with the controls at day 28 (P<0.05). However, new bone formation was not detected at days 7 and 14 in both the groups (P>0.05). CONCLUSION: ASI supplementation significantly improved bone tissue healing in rats with critical-sized defects. This study demonstrated that ASI can enhance bone repair and has potential as a therapeutic regimen in humans. Dove Medical Press 2016-06-27 /pmc/articles/PMC4930222/ /pubmed/27390517 http://dx.doi.org/10.2147/DDDT.S109271 Text en © 2016 Yaman 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
Yaman, Ferhan
Acikan, Izzet
Dundar, Serkan
Simsek, Sercan
Gul, Mehmet
Ozercan, Ibrahim Hanifi
Komorowski, James
Sahin, Kazim
Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
title Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
title_full Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
title_fullStr Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
title_full_unstemmed Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
title_short Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
title_sort dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930222/
https://www.ncbi.nlm.nih.gov/pubmed/27390517
http://dx.doi.org/10.2147/DDDT.S109271
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