Effect of rutin on cisplatin-induced small intestine (Jejunum) damage in rats

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Background and Objective: Cisplatin is an antineoplastic, platinum derivative used in the treatment of various cancers. Mucositis is a notable side effect of cisplatin treatment. Rutin (vitamin P1) is a drug with antioxidant, anticancer, antidiabetic and antimicrobial properties. The aim of this study was to biochemically, histopathologically and immunohistochemically investigate the effect of rutin on cisplatin-induced mucositis of the small intestine (jejunum) in rats. Materials and Methods: Twenty four rats were divided into four groups with six animals in each group: healthy group (HG), cisplatin-only group (CCG), 50 mg kg-1 of rutin plus cisplatin group (RG-50) and 100 mg kg-1 of rutin plus cisplatin group (RG-100). Rutin or distilled water were administered via an oral gavage. One hour after the administration of rutin or distilled water, the CCG, RG-50 and RG-100 were intraperitoneally injected with 5 mg kg-1 of cisplatin once every 2 for 8 days. At the end of this period, all the animals were sacrificed using a high-dose anesthetic and their small intestines (jejunum) were removed for biochemical and histopathological procedures. Differences between the groups were analyzed using a one-way analysis of variance, followed by Dunnett’s multiple comparisons test. Results: The levels of oxidants increased in all the cisplatin-treated groups, whereas those of antioxidants decreased. Rutin administered at a dose of 100 but not 50 mg kg-1 reduced oxidant levels and increased antioxidant levels to those of healthy tissues. Histopathologically, tissue damage was observed in jejunal tissue of the rats administered only cisplatin, whereas treatment with 100 mg kg-1of rutin prevented cisplatin-induced histopathological damage. In the group administered 50 mg kg-1of rutin, jejunal tissue showed a near-normal appearance, except for mildly dilated congested blood vessels. As shown immunohistochemically, rutin prevented cisplatin-induced jejunal damage more effectively when administered at a dose of 100 mg kg-1 than 50 mg kg-1. Conclusion: Rutin may be useful in the prevention of cisplatin-induced jejunal mucositis. © 2018 Ismail Topal et al.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/14240Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3923/ijp.2018.1136.1144Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTopal, Ismail
dc.contributor.authorEmre Akbulut, Ulas
dc.contributor.authorCimen, Orhan
dc.contributor.authorKolkiran, Abdulselim
dc.contributor.authorAkturan, Selcuk
dc.contributor.authorKeskin Cimen, Ferda
dc.contributor.authorCankaya, Murat
dc.contributor.authorOnur Eden, Arif
dc.contributor.authorSuleyman, Zeynep
dc.contributor.authorOzbek Bilgin, Asli
dc.date.accessioned2026-10-18T20:29:01.959988209Z
dc.date.available2026-10-18T20:29:01.959988209Z
dc.date.issued2018
dc.description.abstractBackground and Objective: Cisplatin is an antineoplastic, platinum derivative used in the treatment of various cancers. Mucositis is a notable side effect of cisplatin treatment. Rutin (vitamin P1) is a drug with antioxidant, anticancer, antidiabetic and antimicrobial properties. The aim of this study was to biochemically, histopathologically and immunohistochemically investigate the effect of rutin on cisplatin-induced mucositis of the small intestine (jejunum) in rats. Materials and Methods: Twenty four rats were divided into four groups with six animals in each group: healthy group (HG), cisplatin-only group (CCG), 50 mg kg-1 of rutin plus cisplatin group (RG-50) and 100 mg kg-1 of rutin plus cisplatin group (RG-100). Rutin or distilled water were administered via an oral gavage. One hour after the administration of rutin or distilled water, the CCG, RG-50 and RG-100 were intraperitoneally injected with 5 mg kg-1 of cisplatin once every 2 for 8 days. At the end of this period, all the animals were sacrificed using a high-dose anesthetic and their small intestines (jejunum) were removed for biochemical and histopathological procedures. Differences between the groups were analyzed using a one-way analysis of variance, followed by Dunnett’s multiple comparisons test. Results: The levels of oxidants increased in all the cisplatin-treated groups, whereas those of antioxidants decreased. Rutin administered at a dose of 100 but not 50 mg kg-1 reduced oxidant levels and increased antioxidant levels to those of healthy tissues. Histopathologically, tissue damage was observed in jejunal tissue of the rats administered only cisplatin, whereas treatment with 100 mg kg-1of rutin prevented cisplatin-induced histopathological damage. In the group administered 50 mg kg-1of rutin, jejunal tissue showed a near-normal appearance, except for mildly dilated congested blood vessels. As shown immunohistochemically, rutin prevented cisplatin-induced jejunal damage more effectively when administered at a dose of 100 mg kg-1 than 50 mg kg-1. Conclusion: Rutin may be useful in the prevention of cisplatin-induced jejunal mucositis. © 2018 Ismail Topal et al.
dc.identifier.doi10.3923/ijp.2018.1136.1144
dc.identifier.eissn1812-5700
dc.identifier.endpage1144
dc.identifier.issn1811-7775
dc.identifier.issue8
dc.identifier.scopus2-s2.0-85055543448
dc.identifier.startpage1136
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14240
dc.identifier.volume14
dc.identifier.wosWOS:000452552500011
dc.language.isoen
dc.publisherAsian Network for Scientific Information
dc.relation.ispartofInternational Journal of Pharmacology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCisplatin
dc.subjectIntestinal damage
dc.subjectMucositis
dc.subjectOxidative stress
dc.subjectRutin
dc.subjectToxicity
dc.subjectantioxidant
dc.subjectcatalase
dc.subjectglutathione
dc.subjectglutathione peroxidase
dc.subjectglutathione transferase
dc.subjectmalonaldehyde
dc.subjectnitric oxide
dc.subjectrutoside
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectdrug dose comparison
dc.subjectgastrointestinal toxicity
dc.subjecthistopathology
dc.subjectimmunohistochemistry
dc.subjectinflammatory infiltrate
dc.subjectintestine injury
dc.subjectintestine villus atrophy
dc.subjectjejunum mucosa
dc.subjectjejunum tissue
dc.subjectlipid peroxidation
dc.subjectmale
dc.titleEffect of rutin on cisplatin-induced small intestine (Jejunum) damage in rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos3
rdl.oa.statusopen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)