Publication:
Pressure ulcer-induced oxidative organ injury is ameliorated by beta-glucan treatment in rats

dc.contributor.authorŞENER, GÖKSEL
dc.contributor.authorsSener, G; Sert, G; Sehirli, AO; Arbak, S; Uslu, B; Gedik, N; Ayanoglu-Dulger, G
dc.date.accessioned2022-03-12T17:19:33Z
dc.date.accessioned2026-01-11T10:24:25Z
dc.date.available2022-03-12T17:19:33Z
dc.date.issued2006
dc.description.abstractPressure ulcers (PU) cause morphological and functional alterations in the skin and visceral organs. In this study we investigated the role of oxidative damage in PUs and the probable beneficial effect of beta-glucan treatment against this damage. beta-glucan is known to have immunomodulatory effects. Experiments were carried on Wistar albino rats. PU was induced by applying magnets over steel plates that were implanted under the skin, to compress the skin and cause ischemia where removing the magnets cause reperfusion of the tissue. Within the first 12 h, rats were subjected to 5 cycles of ischemia/reperfusion (I/R), followed by 12 h ischemia. This protocol was repeated for 3 days. In treatment groups, twice a day during reperfusion periods, beta-glucan was either applied locally (25 mg/kg) as an ointment on skin, or administered orally (50 mg/kg) as a gavage. At the end of the experimental periods, tissue samples (skin, liver, kidney, lung, stomach, and ileum) were taken for the measurement of malondialdehyde (MDA) - an index of lipid peroxidation - and glutathione (GSH) - a key antioxidant - levels. Neutrophil infiltration was evaluated by the measurement of tissue myeloperoxidase activity, while collagen contents were measured for the evaluation of tissue fibrosis. Skin tissues were also examined microscopically. Liver and kidney functions were assayed in serum samples. Local treatment with beta-glucan inhibited the increase in MDA and MPO levels and the decrease in GSH in the skin induced by PU, but was less efficient in preventing the damage in visceral organs. However, systemic treatment prevented the damage in the visceral organs. Significant increases in creatinine, BUN, ALT, AST, LDH and collagen levels in PU group were prevented by beta-glucan treatment. The light microscopic examination exhibited significant degenerative changes in dermis and epidermis in the PU group. Tissue injury was decreased especially in the locally treated group. Thus, supplementing geriatric and neurologically impaired patients with adjuvant therapy of beta-glucan may have some benefits for successful therapy and improving quality of life. (c) 2005 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.intimp.2005.10.010
dc.identifier.issn1567-5769
dc.identifier.pubmed16546702
dc.identifier.urihttps://hdl.handle.net/11424/228124
dc.identifier.wosWOS:000236555700002
dc.language.isoeng
dc.publisherELSEVIER SCIENCE BV
dc.relation.ispartofINTERNATIONAL IMMUNOPHARMACOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectbeta-glucan
dc.subjectdecubitus ulcer
dc.subjectglutathione
dc.subjectlipid peroxidation
dc.subjectmyeloperoxidase activity
dc.subjectSTAPHYLOCOCCAL WOUND-INFECTION
dc.subjectGUINEA-PIG MODEL
dc.subjectLIPID-PEROXIDATION
dc.subjectCYTOKINE RELEASE
dc.subjectTISSUE-INJURY
dc.subjectFREE-RADICALS
dc.subjectMELATONIN
dc.subjectACTIVATION
dc.subjectEXPRESSION
dc.subjectMICE
dc.titlePressure ulcer-induced oxidative organ injury is ameliorated by beta-glucan treatment in rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage732
oaire.citation.issue5
oaire.citation.startPage724
oaire.citation.titleINTERNATIONAL IMMUNOPHARMACOLOGY
oaire.citation.volume6

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