Effect of inositol -stabilized arginine silicate on arthritis in a rat model

dc.contributor.authorŞahin, Kazım
dc.contributor.authorOjalvo, Sara Perez
dc.contributor.authorAkdemir, Fatih
dc.contributor.authorOrhan, Cemal
dc.contributor.authorTuzcu, Mehmet
dc.contributor.authorŞahin, Nurhan
dc.contributor.authorKomorowski, James R.
dc.date.accessioned2026-08-12T17:33:56Z
dc.date.issued2019
dc.departmentFırat Üniversitesi
dc.description.abstractThe purpose of this study was to test the effects of arginine-silicate-inositol complex (ASI), compared to a combination of the individual ingredients (A + S + I) of the AM, on inflammatory markers and joint health in a collagen-induced arthritis (CIA) rat model. A total of 28 Wistar rats were divided into four groups: (i) Control; (ii) Arthritic group, rats subjected to CIA induction by injection of bovine collagen type II (A); (iii) Arthritic group treated with equivalent doses of the separate components of the ASI complex (arginine hydrochloride, silicon, and inositol) (A + S + I); (iv) Arthritic group treated with the ASI complex. The ASI complex treatment showed improved inflammation scores and markers over the arthritic control and the A + S + I group. ASI group had also greater levels of serum and joint-tissue arginine and silicon than the A + S + I group. Joint tissue IL-6, NF-kappa B, COX-2, TNF-alpha, p38 MAPK, WISP-1, and beta-Catenin levels were lower in the ASI group compared to the other groups (P < 0.05 for all). In conclusion, these results demonstrate that the ASI complex may be effective in reducing markers of inflammation associated with joint health and that the AM complex is more effective than a combination of the individual ingredients.
dc.description.sponsorshipNutrition 21, LLC (Purchase, NY, USA); Turkish Academy of Sciences (Ankara, Turkey; KS)
dc.description.sponsorshipFunding for this study was provided by Nutrition 21, LLC (Purchase, NY, USA) through a restricted grant. This work was also supported in part by the Turkish Academy of Sciences (Ankara, Turkey; KS).
dc.identifier.doi10.1016/j.fct.2019.01.005
dc.identifier.endpage251
dc.identifier.issn0278-6915
dc.identifier.issn1873-6351
dc.identifier.orcid0000-0002-5779-6631
dc.identifier.orcid0000-0003-4138-7689
dc.identifier.orcid0000-0002-1329-3143
dc.identifier.orcid0000-0001-9542-5244
dc.identifier.orcid0000-0003-4995-430X
dc.identifier.pmid30634014
dc.identifier.scopus2-s2.0-85059813809
dc.identifier.scopusqualityQ1
dc.identifier.startpage242
dc.identifier.urihttps://doi.org/10.1016/j.fct.2019.01.005
dc.identifier.urihttps://hdl.handle.net/11508/57212
dc.identifier.volume125
dc.identifier.wosWOS:000463305000026
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherPergamon-Elsevier Science Ltd
dc.relation.ispartofFood and Chemical Toxicology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectArthritis
dc.subjectArginine
dc.subjectSilicate
dc.subjectInositol
dc.subjectInflammatory cytokines
dc.titleEffect of inositol -stabilized arginine silicate on arthritis in a rat model
dc.typeArticle

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