Publication:
Silymarin, the antioxidant component of Silybum marianum, protects against burn-induced oxidative skin injury

dc.contributor.authorERCAN, FERİHA
dc.contributor.authorŞENER, GÖKSEL
dc.contributor.authorYÜKSEL, MERAL
dc.contributor.authorAKBAY, TUĞBA
dc.contributor.authorsToklu, Hale Z.; Tunah-Akbay, Tuba; Erkani, Gozde; Yuksel, Meral; Ercan, Feriha; Sener, Goksel
dc.date.accessioned2022-03-12T17:32:54Z
dc.date.accessioned2026-01-11T15:19:23Z
dc.date.available2022-03-12T17:32:54Z
dc.date.issued2007
dc.description.abstractBackground: Despite recent advances, severe burn is one of the most common problems faced in the emergency room. Major thermal injury induces the activation of an inflammatory cascade resulting in local tissue damage, to contribute to the development of subsequent damage of multiple organs distant from the original burn wound. Objective: Silymarin, the major component of milk thistle has been shown to have antioxidant properties. In the present study, we investigated the putative antioxidant effect of local or systemic silymarin treatment on burn-induced oxidative tissue injury. Methods: Wistar albino rats were exposed to 90 degrees C bath for 10 s to induce burn. Silymarin either locally (30 mg/kg) applied on 4 cm(2) area or locally + systemically (50 mg/kg, p.o.) was administered after the burn and repeated twice daily. Rats were decapitated 48 h after injury and blood was collected for tumor necrosis factor-a (TNF-alpha) and lactate dehydrogenase (LDH) activity. In skin tissue samples malondialdehyde (MDA) and glutathione (GSH) levels, myeloperoxidase (MPO) activity, and luminol-lucigenin chemiluminescense (CL) were measured in addition to the histological evaluation. Results: Burn caused a significant increase in TNF-a and LDH levels. MDA levels were increased and GSH levels were decreased in the skin at 48 h after-burn. Both local and systemic silymarin treatments significantly reversed these parameters. The raised MPO activity and luminol-lucigenin CL were also significantly decreased. Conclusion: Results indicate that both systemic and local administration of silymarin was effective against burn-induced oxidative damage and morphological alterations in rat skin. Therefore, silymarin merits consideration as a therapeutic agent in the treatment of burns. (C) 2006 Elsevier Ltd and ISBI. All rights reserved.
dc.identifier.doi10.1016/j.burns.2006.10.407
dc.identifier.eissn1879-1409
dc.identifier.issn0305-4179
dc.identifier.pubmed17521818
dc.identifier.urihttps://hdl.handle.net/11424/228719
dc.identifier.wosWOS:000250361600013
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.relation.ispartofBURNS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSilymarin
dc.subjectburn skin
dc.subjectthermal
dc.subjectoxidative
dc.subjectinjury
dc.subjectTHERMAL-INJURY
dc.subjectORGAN DAMAGE
dc.subjectRAT MODEL
dc.subjectLIPID-PEROXIDATION
dc.subjectREACTIVE OXYGEN
dc.subjectSTRESS
dc.subjectINHIBITION
dc.subjectMELATONIN
dc.subjectBLOOD
dc.subjectSTAGE
dc.titleSilymarin, the antioxidant component of Silybum marianum, protects against burn-induced oxidative skin injury
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage916
oaire.citation.issue7
oaire.citation.startPage908
oaire.citation.titleBURNS
oaire.citation.volume33

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