Oxidative and pro-inflammatory lung injury induced by desflurane inhalation in rats and the protective effect of rutin

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Özet

Background. Desflurane is a mainstay of general inhaled anesthetics with a methyl ethyl ether structure and is widely used in clinical practice. It has been reported to induce inflammation and lipid peroxidation in rat pulmonary parenchyma, to increase alveolar macrophages, and to cause peribronchial infiltration and edema. Rutin, a flavonoid vitamin P1, is known to have biological properties including acting as an antioxidant, an anti-inflammatory, and an inhibitor of bronchoalveolar polymorphonuclear leukocyte (PNL) infiltration. Objectives. The aim of this study is to examine the effects of rutin on desflurane-induced pulmonary injury using biochemical and histopathological methods. Materials and methods. The rats were divided into 3 groups (n = 6 each): healthy control (HC), rutin+desflurane-treated (DRT) and desflurane-only (DSF). Briefly, 50 mg/kg of rutin was given orally to the DRT group and an equal volume of normal saline was given to the DSF and HC groups. After 1 h, anesthesia was induced and maintained in the DRT and DSF groups for 2 h. After the rats had been sacrificed, the lungs were removed. Malondialdehyde (MDA), total glutathione (GSH), tumor necrosis factor alpha (TNF-α), and nuclear factor kappa B (NF-κB) levels were measured in the excised lung tissue. The removed tissues were also fixed in 10% formalin, and the obtained sections were stained with hematoxylin and eosin (H&E) and evaluated under light microscopy. The biochemical and histopathological results of the DRT group were compared with those obtained from the DSF and HC groups. Results. Desflurane increased MDA, TNF-α and NF-κB, and decreased GSH in lung tissue. The PNL infiltration, alveolar macrophages, hemorrhage, alveolar damage, and edema were observed in the lung tissue of the DSF group. Rutin was histopathologically shown to protect lung tissue from oxidative stress by preventing an increase in oxidant parameters and a decrease in antioxidants. Conclusions. The results suggest that rutin may be useful in the treatment of desflurane-associated lung injury. © 2021 by Wroclaw Medical University This is an article distributed under the terms of the Creative Commons Attribution 3.0 Unported (CC BY 3.0)

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13317Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17219/acem/136194Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTosun, Mustafa
dc.contributor.authorOlmez, Hasan
dc.contributor.authorUnver, Edhem
dc.contributor.authorArslan, Yusuf Kemal
dc.contributor.authorCimen, Ferda Keskin
dc.contributor.authorOzcicek, Adalet
dc.contributor.authorAktas, Mehmet
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:28:09.533506627Z
dc.date.available2026-10-18T20:28:09.533506627Z
dc.date.issued2021
dc.description.abstractBackground. Desflurane is a mainstay of general inhaled anesthetics with a methyl ethyl ether structure and is widely used in clinical practice. It has been reported to induce inflammation and lipid peroxidation in rat pulmonary parenchyma, to increase alveolar macrophages, and to cause peribronchial infiltration and edema. Rutin, a flavonoid vitamin P1, is known to have biological properties including acting as an antioxidant, an anti-inflammatory, and an inhibitor of bronchoalveolar polymorphonuclear leukocyte (PNL) infiltration. Objectives. The aim of this study is to examine the effects of rutin on desflurane-induced pulmonary injury using biochemical and histopathological methods. Materials and methods. The rats were divided into 3 groups (n = 6 each): healthy control (HC), rutin+desflurane-treated (DRT) and desflurane-only (DSF). Briefly, 50 mg/kg of rutin was given orally to the DRT group and an equal volume of normal saline was given to the DSF and HC groups. After 1 h, anesthesia was induced and maintained in the DRT and DSF groups for 2 h. After the rats had been sacrificed, the lungs were removed. Malondialdehyde (MDA), total glutathione (GSH), tumor necrosis factor alpha (TNF-α), and nuclear factor kappa B (NF-κB) levels were measured in the excised lung tissue. The removed tissues were also fixed in 10% formalin, and the obtained sections were stained with hematoxylin and eosin (H&E) and evaluated under light microscopy. The biochemical and histopathological results of the DRT group were compared with those obtained from the DSF and HC groups. Results. Desflurane increased MDA, TNF-α and NF-κB, and decreased GSH in lung tissue. The PNL infiltration, alveolar macrophages, hemorrhage, alveolar damage, and edema were observed in the lung tissue of the DSF group. Rutin was histopathologically shown to protect lung tissue from oxidative stress by preventing an increase in oxidant parameters and a decrease in antioxidants. Conclusions. The results suggest that rutin may be useful in the treatment of desflurane-associated lung injury. © 2021 by Wroclaw Medical University This is an article distributed under the terms of the Creative Commons Attribution 3.0 Unported (CC BY 3.0)
dc.identifier.doi10.17219/acem/136194
dc.identifier.eissn2451-2680
dc.identifier.endpage948
dc.identifier.issn1899-5276
dc.identifier.issue9
dc.identifier.pmid34418333
dc.identifier.scopus2-s2.0-85114414731
dc.identifier.startpage941
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13317
dc.identifier.volume30
dc.identifier.wosWOS:000704583000008
dc.language.isoen
dc.publisherWroclaw University of Medicine
dc.relation.ispartofAdvances in Clinical and Experimental Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDesflurane
dc.subjectLung injury
dc.subjectOxidative stress
dc.subjectRutin
dc.subjectAnimals
dc.subjectMalondialdehyde
dc.subjectRats
dc.subjectglutathione
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectmalonaldehyde
dc.subjectrutoside
dc.subjectsodium chloride
dc.subjecttumor necrosis factor
dc.subjectanesthesia induction
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectcontrolled study
dc.subjectdrug effect
dc.subjecthistopathology
dc.subjectinhalation anesthesia
dc.subjectlung alveolus macrophage
dc.subjectlung edema
dc.subjectlung hemorrhage
dc.subjectlung parenchyma
dc.subjectmale
dc.titleOxidative and pro-inflammatory lung injury induced by desflurane inhalation in rats and the protective effect of rutin
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus15
rdl.citation.wos15
rdl.departmentDepartment of Chest Diseases, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Biostatistics, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Pathology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Internal Medicine, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Biochemistry, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)