Novel formulations ameliorate osteoarthritis in rats by inhibiting inflammation and oxidative stress

MakaleAçık ErişimScopus SJRQ1
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

The study tested new oral plant-based formulations (F) on rats with monosodium iodoacetate (MIA)-induced osteoarthritis, measuring inflammation, antioxidant levels, paw size, stride, and analyzing knee joint images. Fifty-six female Sprague Dawley rats were allocated into 8 groups: (1) Control, (2) MIA (OA induced with MIA), (3) MIA + F1 [curcuminoids+gingerols+acetyl-11-keto-β boswellic acid (AKBA)], (4) MIA + F2 (curcuminoids+Withania glycosides+AKBA), (5) MIA + F3 (curcuminoids+total withanolides+AKBA), (6) MIA + F4 (curcuminoids, AKBA), (7) MIA + UCII (type II collagen), and (8) MIA + GCHON (Glucosamine Chondroitin). Treatments F1 to F4 reduced right joint diameter and improved stride length and paw area in OA rats. Despite improvements with treatments F1 to F4, there was no significant difference between these groups (p >.05). In OA animals, F1 to F4 treatments decreased MDA levels and increased antioxidant enzymes activities (p <.001). This was done by reducing levels of inflammatory markers and enzymes like IL-1β, IL-6, MMP-8, TNF-α, CRP, COMP, and LOX-5, while increasing the anti-inflammatory cytokine IL-10. In conclusion, these plant-based treatments significantly reduced osteoarthritis severity, slowed disease progression by reducing inflammation, and protected joints from damage, showing a protective effect in rats with induced osteoarthritis, likely due to their anti-inflammatory and antioxidant properties.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/munzur/2121Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/fsn3.4407Yayıncı resmi DOI adresi
İndeks kayıtları
Kaydın indeks veri tabanlarındaki sayfası (aktarımda alınan kayıt numarasıyla). Erişim, indeksin kendi koşullarına bağlıdır.
Atıflar
Scopus
14
WoS
11
OpenAlex
10
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorErten, Fusun
dc.contributor.authorOzdemir, Oguzhan
dc.contributor.authorTokmak, Muhammed
dc.contributor.authorDurmus, Ali Said
dc.contributor.authorOzercan, Ibrahim Hanifi
dc.contributor.authorMorde, Abhijeet
dc.contributor.authorPadigaru, Muralidhara
dc.contributor.authorSahin, Kazim
dc.date.accessioned2026-10-28T14:54:57.756286868Z
dc.date.available2026-10-28T14:54:57.756286868Z
dc.date.issued2024
dc.description.abstractThe study tested new oral plant-based formulations (F) on rats with monosodium iodoacetate (MIA)-induced osteoarthritis, measuring inflammation, antioxidant levels, paw size, stride, and analyzing knee joint images. Fifty-six female Sprague Dawley rats were allocated into 8 groups: (1) Control, (2) MIA (OA induced with MIA), (3) MIA + F1 [curcuminoids+gingerols+acetyl-11-keto-β boswellic acid (AKBA)], (4) MIA + F2 (curcuminoids+Withania glycosides+AKBA), (5) MIA + F3 (curcuminoids+total withanolides+AKBA), (6) MIA + F4 (curcuminoids, AKBA), (7) MIA + UCII (type II collagen), and (8) MIA + GCHON (Glucosamine Chondroitin). Treatments F1 to F4 reduced right joint diameter and improved stride length and paw area in OA rats. Despite improvements with treatments F1 to F4, there was no significant difference between these groups (p >.05). In OA animals, F1 to F4 treatments decreased MDA levels and increased antioxidant enzymes activities (p <.001). This was done by reducing levels of inflammatory markers and enzymes like IL-1β, IL-6, MMP-8, TNF-α, CRP, COMP, and LOX-5, while increasing the anti-inflammatory cytokine IL-10. In conclusion, these plant-based treatments significantly reduced osteoarthritis severity, slowed disease progression by reducing inflammation, and protected joints from damage, showing a protective effect in rats with induced osteoarthritis, likely due to their anti-inflammatory and antioxidant properties.
dc.description.sponsorshipOmniActive Health Technologies
dc.description.sponsorshipTürkiye Bilimler Akademisi
dc.description.sponsorshipTUBA
dc.identifier.doi10.1002/fsn3.4407
dc.identifier.endpage7912
dc.identifier.issn2048-7177
dc.identifier.issue10
dc.identifier.pmcidPMC11521736
dc.identifier.pmid39479600
dc.identifier.scopus2-s2.0-85201042984
dc.identifier.startpage7896
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2121
dc.identifier.volume12
dc.identifier.wosWOS:001289779900001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofFood Science and Nutrition
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectanti-inflammatory
dc.subjectinflammation
dc.subjectosteoarthritis
dc.subjectoxidative stress
dc.subjectplant-based formulations
dc.subject.classificationFood Science & Technology
dc.subject.otherCARTILAGE
dc.subject.otherSYSTEM
dc.titleNovel formulations ameliorate osteoarthritis in rats by inhibiting inflammation and oxidative stress
dc.typeArticle
rdl.citation.openalex10
rdl.citation.scopus14
rdl.citation.wos11
rdl.departmentDepartment of Veterinary Medicine, Pertek Sakine Genc Vocational School Munzur University Tunceli Turkey
rdl.departmentDepartment of Veterinary Science, Technical Sciences Vocational School Batman University Batman Turkey
rdl.departmentDepartment of Animal Nutrition, Faculty of Veterinary Medicine Firat University Elazig Turkey
rdl.departmentDepartment of Surgery, Faculty of Veterinary Medicine Firat University Elazig Turkey
rdl.departmentDepartment of Pathology, Faculty of Medicine Firat University Elazig Turkey
rdl.departmentResearch and Development OmniActive Health Technologies Mumbai India
rdl.oa.statushybrid
rdl.oa.statusgreen
rdl.oa.urlhttps://doi.org/10.1002/fsn3.4407
rdl.scopus.quartileQ1
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)