Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
| dc.contributor.author | Yaman, Ferhan | |
| dc.contributor.author | Acikan, Izzet | |
| dc.contributor.author | Dundar, Serkan | |
| dc.contributor.author | Simsek, Sercan | |
| dc.contributor.author | Gul, Mehmet | |
| dc.contributor.author | Ozercan, Ibrahim Hanifi | |
| dc.contributor.author | Şahin, Kazım | |
| dc.date.accessioned | 2026-08-12T17:48:53Z | |
| dc.date.issued | 2016 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | Turkish Academy of Sciences | |
| dc.description.sponsorship | The authors thank Nutrition 21 Inc (NY, USA) for providing ASI complex. This work was supported in part by the Turkish Academy of Sciences (KS). | |
| dc.identifier.doi | 10.2147/DDDT.S109271 | |
| dc.identifier.endpage | 2086 | |
| dc.identifier.issn | 1177-8881 | |
| dc.identifier.orcid | 0000-0001-9542-5244 | |
| dc.identifier.orcid | 0000-0002-5721-8778 | |
| dc.identifier.pmid | 27390517 | |
| dc.identifier.scopus | 2-s2.0-84976545032 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 2081 | |
| dc.identifier.uri | https://doi.org/10.2147/DDDT.S109271 | |
| dc.identifier.uri | https://hdl.handle.net/11508/61593 | |
| dc.identifier.volume | 10 | |
| dc.identifier.wos | WOS:000378917700006 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Dove Medical Press Ltd | |
| dc.relation.ispartof | Drug Design Development and Therapy | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WoS_20260511 | |
| dc.subject | arginine silicate inositol | |
| dc.subject | bone healing | |
| dc.subject | osteoblast | |
| dc.subject | osteoclast | |
| dc.subject | critical-sized defect | |
| dc.title | Dietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study | |
| dc.type | Article |







