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

dc.contributor.authorYaman, Ferhan
dc.contributor.authorAcikan, Izzet
dc.contributor.authorDundar, Serkan
dc.contributor.authorSimsek, Sercan
dc.contributor.authorGul, Mehmet
dc.contributor.authorOzercan, Ibrahim Hanifi
dc.contributor.authorŞahin, Kazım
dc.date.accessioned2026-08-12T17:48:53Z
dc.date.issued2016
dc.departmentFırat Üniversitesi
dc.description.abstractBackground: 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.sponsorshipTurkish Academy of Sciences
dc.description.sponsorshipThe 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.doi10.2147/DDDT.S109271
dc.identifier.endpage2086
dc.identifier.issn1177-8881
dc.identifier.orcid0000-0001-9542-5244
dc.identifier.orcid0000-0002-5721-8778
dc.identifier.pmid27390517
dc.identifier.scopus2-s2.0-84976545032
dc.identifier.scopusqualityQ1
dc.identifier.startpage2081
dc.identifier.urihttps://doi.org/10.2147/DDDT.S109271
dc.identifier.urihttps://hdl.handle.net/11508/61593
dc.identifier.volume10
dc.identifier.wosWOS:000378917700006
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherDove Medical Press Ltd
dc.relation.ispartofDrug Design Development and Therapy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectarginine silicate inositol
dc.subjectbone healing
dc.subjectosteoblast
dc.subjectosteoclast
dc.subjectcritical-sized defect
dc.titleDietary arginine silicate inositol complex increased bone healing: histologic and histomorphometric study
dc.typeArticle

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