Use of ozone to treat ileostomy dermatitis in an experimental rat model

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Özet

Background: Dermatitis associated with ileostomy is an important problem that affects many people, especially children. The aim of this study was to investigate the therapeutic effects of ozone on dermatitis due to ileostomy, and to develop an alternative treatment option. Material/Methods: A total of 28 rats were divided into 4 groups: control, ileostomy, ozone, and zinc oxide. Ileostomy was performed in all rats except the control group. After a 1-week waiting time, the ozone group was administered ozone therapy and the zinc oxide group was administered zinc oxide cream locally once a day for a total of 7 days. All rats were sacrificed at the end of this period. The efficacy of treatment was examined by biochemical, histopathological, and immunohistochemical parameters. The levels of malondialdehyde (MDA), total glutathione (tGSH), total antioxidant capacity (TAC), and total oxidant status (TOS) were measured from tissue. Vascular endothelial growth factor (VEGF) and proliferating cell nuclear antigen (PCNA) were examined immunohistochemically. Results: Dermatitis occurred pathologically in all rats that underwent ileostomy surgery. The lowest dermatitis score was in the ozone treatment group (p<0.05). Ileostomy dermatitis caused increased levels of MDA and TOS. Ozone treatment resulted in reduced MDA and TOS levels, while the levels of tGSH and TAC were increased (p<0.05). Both VEGF and PCNA immunostaining were augmented in the ozone treatment group (p<0.05). Conclusions: Local ozone application may be a good alternative compared to the conventional treatment methods for the prevention of skin lesions that develop after ileostomy. © Med Sci Monit, 2016.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15117Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.12659/msm.897696Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBiçer, Şenol
dc.contributor.authorSayar, İlyas
dc.contributor.authorGürsul, Cebrail
dc.contributor.authorIşık, Arda
dc.contributor.authorAydın, Merve
dc.contributor.authorPeker, Kemal
dc.contributor.authorDemiryilmaz, İsmail
dc.date.accessioned2026-10-18T20:29:54.338963993Z
dc.date.available2026-10-18T20:29:54.338963993Z
dc.date.issued2016
dc.description.abstractBackground: Dermatitis associated with ileostomy is an important problem that affects many people, especially children. The aim of this study was to investigate the therapeutic effects of ozone on dermatitis due to ileostomy, and to develop an alternative treatment option. Material/Methods: A total of 28 rats were divided into 4 groups: control, ileostomy, ozone, and zinc oxide. Ileostomy was performed in all rats except the control group. After a 1-week waiting time, the ozone group was administered ozone therapy and the zinc oxide group was administered zinc oxide cream locally once a day for a total of 7 days. All rats were sacrificed at the end of this period. The efficacy of treatment was examined by biochemical, histopathological, and immunohistochemical parameters. The levels of malondialdehyde (MDA), total glutathione (tGSH), total antioxidant capacity (TAC), and total oxidant status (TOS) were measured from tissue. Vascular endothelial growth factor (VEGF) and proliferating cell nuclear antigen (PCNA) were examined immunohistochemically. Results: Dermatitis occurred pathologically in all rats that underwent ileostomy surgery. The lowest dermatitis score was in the ozone treatment group (p<0.05). Ileostomy dermatitis caused increased levels of MDA and TOS. Ozone treatment resulted in reduced MDA and TOS levels, while the levels of tGSH and TAC were increased (p<0.05). Both VEGF and PCNA immunostaining were augmented in the ozone treatment group (p<0.05). Conclusions: Local ozone application may be a good alternative compared to the conventional treatment methods for the prevention of skin lesions that develop after ileostomy. © Med Sci Monit, 2016.
dc.description.sponsorshipThis research was supported by Erzincan University Unit of Scientific Projects (no. 2014-14/18), Erzincan, Turkey
dc.identifier.doi10.12659/msm.897696
dc.identifier.endpage765
dc.identifier.issn1234-1010
dc.identifier.pmcidPMC4784547
dc.identifier.pmid26947591
dc.identifier.scopus2-s2.0-84960424440
dc.identifier.startpage757
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15117
dc.identifier.volume22
dc.identifier.wosWOS:000371726200001
dc.language.isoen
dc.publisherInternational Scientific Literature Inc.
dc.relation.ispartofMedical Science Monitor
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDermatitis
dc.subjectIleostomy
dc.subjectImmunohistochemistry
dc.subjectOzone
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectDisease Models, Animal
dc.subjectGlutathione
dc.subjectMalondialdehyde
dc.subjectOxidants
dc.subjectRats, Sprague-Dawley
dc.subjectcycline
dc.subjectmalonaldehyde
dc.subjectvasculotropin
dc.subjectzinc oxide
dc.subjectantioxidant
dc.subjectoxidizing agent
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant assay
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectcontrolled study
dc.subjectenzyme linked immunosorbent assay
dc.subjectexperimental rat
dc.subjecthistopathology
dc.subjectmicroscopy
dc.subjectnonhuman
dc.subjectozone therapy
dc.titleUse of ozone to treat ileostomy dermatitis in an experimental rat model
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus8
rdl.citation.wos5
rdl.departmentDepartment of Pediatric Surgery, Erzincan University, Faculty of Medicine, Erzincan, Turkey. | Department of Pathology, Erzincan University, Faculty of Medicine, Erzincan, Turkey. | Department of Physiology, Erzincan University, Faculty of Medicine, Erzincan, Turkey. | Department of General Surgery, Erzincan University, Faculty of Medicine, Erzincan, Turkey. | Department of Microbiology, Erzincan University, Faculty of Medicine, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)