Suberosin Alleviates Sepsis-Induced Lung Injury in A Rat Model of Cecal Ligation and Puncture

MakaleAçık ErişimScopus SJRQ2
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Özet

Background/aims: Sepsis is one of the major problems encountered in intensive care units, causing organ damage and increasing mortality. Suberosin (SBR) is a type of coumarin with antioxidant and anti-inflammatory activities. The goal of this study is to explore the protective effects of SBR on the lungs in a rat model of sepsis. Methods: Male Wistar rats were utilized in this study. A cecal ligation and puncture (CLP) model was applied to induce sepsis. Rats were separated into six groups with nine animals in each group, including healthy control, SBR, CLP, and CLP + SBR (5, 10, and 20 mg/kg) groups. Superoxide dismutase (SOD), glutathione (GSH) enzyme activities, and malondialdehyde (MDA) level were measured via enzyme-linked immunosorbent assay (ELISA). The messenger RNA (mRNA) expressions of tumor necrosis factor α (TNF-α) and interleukin 1β (IL-1β) were evaluated by real-time polymerase chain reaction (RT-PCR). Histopathological changes in the lungs were investigated with hematoxylin and eosin (H&E). Results: MDA levels and GSH and SOD enzyme activities were negatively affected in the CLP group, but SBR treatment ameliorated these oxidative stress parameters in the SBR1-3 groups (p< 0.05). The mRNA expressions of TNF-α and IL-1β were increased in the CLP group, and SBR treatment decreased those expression levels in a dose-dependent manner (p < 0.05). Organ damage and necrosis were seen in the CLP group and were alleviated in the SBR3 group. Immunohistochemical (IHC) analysis of lung tissues demonstrated decreased TNF-α and IL-1β immunopositivity in the SBR1-3 groups (p< 0.05). Conclusions: SBR ameliorated sepsis-related lung injury in a dose-dependent manner. This compound has significant potential as a future agent in the treatment of sepsis.

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AlanDeğerDil
dc.contributor.authorKarabulut Uzunçakmak, Sevgi
dc.contributor.authorHalıcı, Zekai
dc.contributor.authorKarakaya, Songül
dc.contributor.authorKutlu, Zerrin
dc.contributor.authorSağlam, Yavuz Selim
dc.contributor.authorBolat, İsmail
dc.contributor.authorAydın, Pelin
dc.contributor.authorKılıç, Ceyda Sibel
dc.date.accessioned2026-10-29T19:08:54.305167511Z
dc.date.available2026-10-29T19:08:54.305167511Z
dc.date.issued2023
dc.description.abstractBackground/aims: Sepsis is one of the major problems encountered in intensive care units, causing organ damage and increasing mortality. Suberosin (SBR) is a type of coumarin with antioxidant and anti-inflammatory activities. The goal of this study is to explore the protective effects of SBR on the lungs in a rat model of sepsis. Methods: Male Wistar rats were utilized in this study. A cecal ligation and puncture (CLP) model was applied to induce sepsis. Rats were separated into six groups with nine animals in each group, including healthy control, SBR, CLP, and CLP + SBR (5, 10, and 20 mg/kg) groups. Superoxide dismutase (SOD), glutathione (GSH) enzyme activities, and malondialdehyde (MDA) level were measured via enzyme-linked immunosorbent assay (ELISA). The messenger RNA (mRNA) expressions of tumor necrosis factor α (TNF-α) and interleukin 1β (IL-1β) were evaluated by real-time polymerase chain reaction (RT-PCR). Histopathological changes in the lungs were investigated with hematoxylin and eosin (H&E). Results: MDA levels and GSH and SOD enzyme activities were negatively affected in the CLP group, but SBR treatment ameliorated these oxidative stress parameters in the SBR1-3 groups (p< 0.05). The mRNA expressions of TNF-α and IL-1β were increased in the CLP group, and SBR treatment decreased those expression levels in a dose-dependent manner (p < 0.05). Organ damage and necrosis were seen in the CLP group and were alleviated in the SBR3 group. Immunohistochemical (IHC) analysis of lung tissues demonstrated decreased TNF-α and IL-1β immunopositivity in the SBR1-3 groups (p< 0.05). Conclusions: SBR ameliorated sepsis-related lung injury in a dose-dependent manner. This compound has significant potential as a future agent in the treatment of sepsis.
dc.identifier.doi10.1080/08941939.2022.2136802
dc.identifier.eissn1521-0553
dc.identifier.endpage9
dc.identifier.issn0894-1939
dc.identifier.issue1
dc.identifier.pmid36345760
dc.identifier.scopus2-s2.0-85141894711
dc.identifier.startpage1
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/11870
dc.identifier.volume36
dc.identifier.wosWOS:000879947700001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofJournal of Investigative Surgery
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectlung injury
dc.subjectoxidative stress
dc.subjectrat
dc.subjectsepsis
dc.subjectsuberosin
dc.subject.classificationSurgery
dc.subject.otherAnimals
dc.subject.otherCoumarins
dc.subject.otherDisease Models, Animal
dc.subject.otherGlutathione
dc.subject.otherLigation
dc.subject.otherLung
dc.subject.otherLung Injury
dc.subject.otherMale
dc.subject.otherPunctures
dc.subject.otherRats
dc.subject.otherRats, Wistar
dc.subject.otherRNA, Messenger
dc.subject.otherSepsis
dc.subject.otherSuperoxide Dismutase
dc.subject.otherTumor Necrosis Factor-alpha
dc.subject.otheradhesive agent
dc.subject.otherantioxidant
dc.subject.otherbeta actin
dc.subject.othercomplementary DNA
dc.subject.othercoumarin
dc.subject.otherdiaminobenzidine
dc.subject.otherdistilled water
dc.subject.othereosin
dc.subject.otherformaldehyde
dc.subject.otherhematoxylin
dc.subject.otherinterleukin 1beta
dc.subject.otherketamine
dc.subject.othermalonaldehyde
dc.subject.othermessenger RNA
dc.subject.othernuclease
dc.subject.otheroxidizing agent
dc.subject.otherparaffin
dc.subject.otherperoxidase
dc.subject.otherphosphate buffered saline
dc.subject.otherprotein
dc.subject.othersodium chloride
dc.subject.othersuberosin
dc.subject.othertumor necrosis factor
dc.subject.otherunclassified drug
dc.subject.otherxylazine
dc.subject.otherxylene
dc.subject.othercoumarin derivative
dc.subject.otherabdominal cavity
dc.subject.otheranimal experiment
dc.subject.otheranimal model
dc.subject.otheranimal tissue
dc.subject.otherantigen retrieval
dc.subject.otherApiaceae
dc.subject.otherArticle
dc.subject.otherbiochemical analysis
dc.subject.otherbody weight
dc.subject.otherbronchiole
dc.subject.otherbronchiole epithelium
dc.subject.otherbronchus
dc.subject.otherbronchus epithelium
dc.subject.othercecal ligation and puncture-induced sepsis
dc.subject.othercell infiltration
dc.subject.othercontrolled study
dc.subject.otherdegeneration
dc.subject.otherdesquamation
dc.subject.otherdrug effect
dc.subject.otherenzyme activity
dc.subject.otherenzyme linked immunosorbent assay
dc.subject.otherepithelium
dc.subject.otherFerulago cassia
dc.subject.othergene expression profiling
dc.subject.otherhistopathology
dc.subject.otherhousekeeping gene
dc.subject.otherincision
dc.subject.otherinflammatory cell
dc.subject.otherlaparotomy
dc.subject.otherlight dark cycle
dc.subject.otherlung alveolus wall
dc.subject.otherlung parenchyma
dc.subject.othermononuclear cell
dc.subject.othermRNA expression level
dc.subject.othernecrosis
dc.subject.othernonhuman
dc.subject.otheroxidative stress
dc.subject.otherperivascular cell
dc.subject.otherprotein expression
dc.subject.otherrat
dc.subject.otherreal time polymerase chain reaction
dc.subject.otherRNA extraction
dc.subject.othervenous congestion
dc.subject.otheradverse event
dc.subject.otheranimal
dc.subject.othercomplication
dc.subject.otherdisease model
dc.subject.othermetabolism
dc.subject.otherpathology
dc.subject.otherpuncture
dc.subject.otherWistar rat
dc.titleSuberosin Alleviates Sepsis-Induced Lung Injury in A Rat Model of Cecal Ligation and Puncture
dc.typeArticle
rdl.citation.openalex15
rdl.citation.scopus15
rdl.citation.wos11
rdl.departmentHealth Services Vocational School, Bayburt University, Bayburt, Turkey
rdl.departmentDepartment of Pharmacology, Faculty of Medicine, Atatürk University, Erzurum, Turkey
rdl.departmentClinical Research, Development and Design Application and Research Center, Ataturk University, Erzurum, Turkey
rdl.departmentDepartment of Pharmaceutical Botany, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey
rdl.departmentDepartment of Biochemistry, Faculty of Pharmacy, Atatürk University, Erzurum, Turkey
rdl.departmentDepartment of Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey
rdl.departmentDepartment of Anesthesia, Regional Education and Research Hospital, Erzurum, Turkey
rdl.departmentDepartment of Pharmaceutical Botany, Faculty of Pharmacy, Ankara University, Ankara, Turkey
rdl.oa.statushybrid
rdl.oa.urlhttps://doi.org/10.1080/08941939.2022.2136802
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)