Effects of silymarin on methotrexate-induced nephrotoxicity in rats

dc.contributor.authorDabak, Durrin Ozlem
dc.contributor.authorKocaman, Nevin
dc.date.accessioned2026-08-12T17:48:31Z
dc.date.issued2015
dc.departmentFırat Üniversitesi
dc.description.abstractMethotrexate (MTX) is widely used in the treatment of various malignancies and nononcological diseases but its use has been limited by its nephrotoxicity. Silymarin (SLY), a natural flavonoid, has been reported to have antioxidant, anti-inflammatory and anti-apoptotic effects. This study was carried out to determine whether SLY exerts a protective effect against MTX-induced nephrotoxicity. Rats were divided into six groups: Group 1 (saline, i.p., single injection), Group 2 (0.5% carboxymethyl cellulose (CMC), by gavage once daily for five consecutive days), Group 3 (SLY, 300 mg/kg per day, i. p. for five consecutive days), Group 4 (MTX, 20 mg/kg, i.p., single injection), Group 5 (MTX + CMC similarly as groups 2 and 4) and Group 6 (MTX + CMC + SLY similarly as groups 2, 3 and 4). Histopathologic alterations including apoptotic changes of the kidney were evaluated. MTX injection exhibited dilated Bowman's space, inflammatory cell infiltration, glomerular and peritubular vascular congestion and swelling of renal tubular epithelium cells. Apoptotic cell death was also markedly increased in renal tubules after MTX administration. SLY treatment resulted in statistically significant amelioration in the histological alterations and reduced the number of TUNEL-positive cells as compared with the MTX treated rats (p < 0.05). In conclusion, SLY treatment leads to a reduction on MTX-induced renal damage in rats. Since SLY is safe and acceptable for human consumption, further studies to define the exact mechanism of the protecting effect of SLY on MTX-induced nephrotoxicity and the optimum dosage of this compound would be useful.
dc.description.sponsorshipFirat University Scientific Research Projects Management Unit (FUBAP) [TF1152]
dc.description.sponsorshipThis research was supported by Firat University Scientific Research Projects Management Unit (FUBAP) project number TF1152.
dc.identifier.doi10.3109/0886022X.2015.1012984
dc.identifier.endpage739
dc.identifier.issn0886-022X
dc.identifier.issn1525-6049
dc.identifier.issue4
dc.identifier.orcid0000-0001-7210-6873
dc.identifier.pmid25707519
dc.identifier.scopus2-s2.0-84930322191
dc.identifier.scopusqualityQ2
dc.identifier.startpage734
dc.identifier.urihttps://doi.org/10.3109/0886022X.2015.1012984
dc.identifier.urihttps://hdl.handle.net/11508/61455
dc.identifier.volume37
dc.identifier.wosWOS:000355941500030
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofRenal Failure
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectApoptosis
dc.subjectmethotrexate
dc.subjectnephrotoxicity
dc.subjectrat
dc.subjectsilymarin
dc.titleEffects of silymarin on methotrexate-induced nephrotoxicity in rats
dc.typeArticle

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