Protective effect of melatonin and ascorbic acid combination on sepsis-induced lung injury: An Experimental study

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Özet

This study investigated the synergistic protective effects of melatonin (MEL) and ascorbic acid (vitamin C, ASA) in treating sepsis-induced lung injury in rats. Rats were divided into five groups: control, cecal ligation and puncture (CLP), CLP + MEL, CLP + ASA and CLP + MEL + ASA. The effects of MEL (10 mg/kg), ASA (100 mg/kg) and their combination on oxidative stress, inflammation and histopathology were evaluated in septic rats’ lung tissues. Sepsis-induced oxidative stress and inflammation were evident through increased levels of malondialdehyde (MDA), myeloperoxidase (MPO), total oxidant status (TOS) and oxidative stress index (OSI); decreased levels of superoxide dismutase (SOD), glutathione (GSH), catalase (CAT) and glutathione peroxidase (GPx); and elevated levels of tumour necrosis factor-α (TNF-α) and interleukin-1 β (IL-1β) in the lung tissue. Treatment with MEL, ASA and their combination significantly improved antioxidant capacity and reduced oxidative stress, with the combination treatment being more effective. The combination treatment also significantly reduced TNF-α and IL-1β levels and improved peroxisome proliferator-activated receptor (PPAR), arylesterase (ARE) and paraoxonase (PON) levels in the lung tissue. Histopathological examination showed reduced oedema and lymphocyte infiltration with a lung tissue appearance similar to the control group. Immunohistochemical staining for caspase 3 demonstrated reduced immune positivity in the treatment groups. In conclusion, this study supports the potential synergistic protective effects of MEL and ASA in treating sepsis-induced lung injury. The combination therapy could effectively reduce oxidative stress, inflammation and improve antioxidant capacity in septic rats, suggesting a promising strategy for treating sepsis-induced lung injury. © 2023 The Authors. Clinical and Experimental Pharmacology and Physiology published by John Wiley & Sons Australia, Ltd.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12395Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1111/1440-1681.13780Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorÜstündağ, Hilal
dc.contributor.authorDemir, Özlem
dc.contributor.authorÇiçek, Betül
dc.contributor.authorHuyut, Mehmet Tahir
dc.contributor.authorYüce, Neslihan
dc.contributor.authorTavacı, Taha
dc.date.accessioned2026-10-18T20:27:18.201076150Z
dc.date.available2026-10-18T20:27:18.201076150Z
dc.date.issued2023
dc.description.abstractThis study investigated the synergistic protective effects of melatonin (MEL) and ascorbic acid (vitamin C, ASA) in treating sepsis-induced lung injury in rats. Rats were divided into five groups: control, cecal ligation and puncture (CLP), CLP + MEL, CLP + ASA and CLP + MEL + ASA. The effects of MEL (10 mg/kg), ASA (100 mg/kg) and their combination on oxidative stress, inflammation and histopathology were evaluated in septic rats’ lung tissues. Sepsis-induced oxidative stress and inflammation were evident through increased levels of malondialdehyde (MDA), myeloperoxidase (MPO), total oxidant status (TOS) and oxidative stress index (OSI); decreased levels of superoxide dismutase (SOD), glutathione (GSH), catalase (CAT) and glutathione peroxidase (GPx); and elevated levels of tumour necrosis factor-α (TNF-α) and interleukin-1 β (IL-1β) in the lung tissue. Treatment with MEL, ASA and their combination significantly improved antioxidant capacity and reduced oxidative stress, with the combination treatment being more effective. The combination treatment also significantly reduced TNF-α and IL-1β levels and improved peroxisome proliferator-activated receptor (PPAR), arylesterase (ARE) and paraoxonase (PON) levels in the lung tissue. Histopathological examination showed reduced oedema and lymphocyte infiltration with a lung tissue appearance similar to the control group. Immunohistochemical staining for caspase 3 demonstrated reduced immune positivity in the treatment groups. In conclusion, this study supports the potential synergistic protective effects of MEL and ASA in treating sepsis-induced lung injury. The combination therapy could effectively reduce oxidative stress, inflammation and improve antioxidant capacity in septic rats, suggesting a promising strategy for treating sepsis-induced lung injury. © 2023 The Authors. Clinical and Experimental Pharmacology and Physiology published by John Wiley & Sons Australia, Ltd.
dc.identifier.doi10.1111/1440-1681.13780
dc.identifier.eissn1440-1681
dc.identifier.endpage646
dc.identifier.issn0305-1870
dc.identifier.issue8
dc.identifier.pmid37199082
dc.identifier.scopus2-s2.0-85159577199
dc.identifier.startpage634
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12395
dc.identifier.volume50
dc.identifier.wosWOS:000991702400001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofClinical and Experimental Pharmacology and Physiology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant
dc.subjectascorbic acid
dc.subjectcaspase 3
dc.subjectinflammation
dc.subjectlung injury
dc.subjectmelatonin
dc.subjectoxidative stress
dc.subjectsepsis
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectGlutathione
dc.subjectLung
dc.subjectRats
dc.subjectTumor Necrosis Factor-alpha
dc.subjectaryldialkylphosphatase
dc.subjectarylesterase
dc.subjectcatalase
dc.subjectglutathione peroxidase
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectmyeloperoxidase
dc.subjectoxidizing agent
dc.subjectperoxisome proliferator activated receptor
dc.subjectphenylacetic acid
dc.subjectsuperoxide dismutase
dc.subjecttumor necrosis factor
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.titleProtective effect of melatonin and ascorbic acid combination on sepsis-induced lung injury: An Experimental study
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus17
rdl.citation.wos18
rdl.departmentDepartment of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | Department of Histology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | Department of Biostatistics, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)