Protective Effects of Thymoquinone and Methotrexate on the Renal Injury in Collagen-Induced Arthritis

dc.contributor.author Budancamanak, Mustafa
dc.contributor.author Kanter, Mehmet
dc.contributor.author Demirel, Adnan
dc.contributor.author Ocakci, Ayse
dc.contributor.author Uysal, Hamdi
dc.contributor.author Karakaya, Cengiz
dc.date.accessioned 2025-05-10T17:07:23Z
dc.date.available 2025-05-10T17:07:23Z
dc.date.issued 2006
dc.description.abstract The goal of this investigation was to study the protective effects of thymoquinone (TQ) and methotrexate (MTX) on collagen-induced arthritis (CIA) in rats. On day 0 under ether anesthesia, the experimental groups were immunized with 0.5 mg native chick collagen II (CII) solubilized in 0.1 M acetic acid and emulsified in Freund's incomplete adjuvant. Control rats were gavaged with vehicle, whereas CII was administered intradermally. In addition, arthritis treated with TQ group received TQ (10 mg kg(-1) stop bw by gavage once a week for 3 weeks starting on day 0); and arthritis treated with MTX group received MTX (MTX was suspended in corn oil and administered by gavage at 1 mg kg(-1) stop bw once a week for 3 weeks starting on day 0). A significant decrease in the incidence and severity of arthritis by clinical and radiographic assessments was found in recipients of therapy, compared with that of controls. The MTX treatment significantly (P < 0.01) decreased the elevated serum NO, urea and creatinine in arthritic rats. Likewise, TQ treatment was also able to reduce significantly (P < 0.05) serum NO, urea and creatinine levels, but to lesser extent than MTX. The histopathologic abnormalities are consistent with the hydropic epithelial cell degenerations and moderate tubular dilatation in the some proximal and distal tubules. The severity of the degenerative changes in most of the shrunken glomerules and vascular congestion were also observed in arthritic animals. Preventive treatment of TQ and especially MTX significantly inhibited kidney dysfunction and this histopathologic alterations. These studies indicate that TQ can be used similar to MTX as a safe and effective therapy for CIA and may be useful in the treatment of rheumatoid arthritis. en_US
dc.identifier.doi 10.1007/s00204-006-0094-0
dc.identifier.issn 0340-5761
dc.identifier.issn 1432-0738
dc.identifier.scopus 2-s2.0-33751437702
dc.identifier.uri https://doi.org/10.1007/s00204-006-0094-0
dc.identifier.uri https://hdl.handle.net/20.500.14720/6750
dc.language.iso en en_US
dc.publisher Springer Heidelberg en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Thymoquinone en_US
dc.subject Methotrexate en_US
dc.subject Renal Injury en_US
dc.subject Collagen-Induced Arthritis en_US
dc.subject Rat en_US
dc.title Protective Effects of Thymoquinone and Methotrexate on the Renal Injury in Collagen-Induced Arthritis en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 11238947300
gdc.author.scopusid 7006356462
gdc.author.scopusid 15076677000
gdc.author.scopusid 10141410600
gdc.author.scopusid 12797394300
gdc.author.scopusid 6508027000
gdc.author.wosid Demirel, Adnan/Gwc-0241-2022
gdc.author.wosid Uysal, Hamdi/Aaf-9708-2020
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp Trakya Univ, Dept Histol & Embryol, Fac Med, Edirne, Turkey; Yuzuncu Yil Univ, Fac Med, Dept Rheumatol, Van, Turkey; Zonguldak Karaelmas Univ, Dept Hlth, High Sch, Zonguldak, Turkey; Ankara Univ, Fac Med Vet, Dept Biochem, TR-06100 Ankara, Turkey; Yuzuncu Yil Univ, Fac Med, Dept Biochem, Van, Turkey en_US
gdc.description.endpage 776 en_US
gdc.description.issue 11 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 768 en_US
gdc.description.volume 80 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 16609887
gdc.identifier.wos WOS:000242294800007
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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