Hispidulin exerts a protective effect against oleic acid induced-ARDS in the rat via inhibition of ACE activity and MAPK pathway

ArticleAçık Erişim

Özet

This study investigates the protective role of Hispidulin on acute respiratory distress syndrome (ARDS) in rats. Rats were divided into three groups: control, ARDS, ARDS+ Hispidulin. The ARDS models were established by injecting rats with oleic acid. Hispidulin (100 mg/kg) was injected i.p. an hour before ARDS. Myeloperoxidase (MPO), Interleukin-8 (IL-8), Mitogen-activated protein kinases (MAPK), Lipid Peroxidation (LPO), Superoxide Dismutase (SOD), Glutathione (GSH), and Angiotensin-converting enzyme (ACE) were determined by ELISA. Tumor necrosis factor-alpha (TNF-α) expression was described by RT-qPCR. Caspase-3 immunostaining was performed to evaluate apoptosis. Compared with the model group, a significant decrease was observed in the MPO, IL-8, MAPK, ACE, LPO levels, and TNF-α expression in the ARDS+ Hispidulin group. Moreover, reduced caspase-3 immunoreactivity and activity of ACE were detected in the Hispidulin+ARDS group. The protective effect of Hispidulin treatment may act through inhibition of the ACE activity and then regulation of inflammatory cytokine level and alteration of apoptosis. © 2023 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorKoc, Kubra
dc.contributor.authorOzek, Nihal Simsek
dc.contributor.authorAysin, Ferhunde
dc.contributor.authorDemir, Ozlem
dc.contributor.authorYilmaz, Asli
dc.contributor.authorYilmaz, Mehmet
dc.contributor.authorGeyikoglu, Fatime
dc.contributor.authorErol, Huseyin Serkan
dc.date.accessioned2026-10-18T20:26:34.445960284Z
dc.date.available2026-10-18T20:26:34.445960284Z
dc.date.issued2024
dc.description.abstractThis study investigates the protective role of Hispidulin on acute respiratory distress syndrome (ARDS) in rats. Rats were divided into three groups: control, ARDS, ARDS+ Hispidulin. The ARDS models were established by injecting rats with oleic acid. Hispidulin (100 mg/kg) was injected i.p. an hour before ARDS. Myeloperoxidase (MPO), Interleukin-8 (IL-8), Mitogen-activated protein kinases (MAPK), Lipid Peroxidation (LPO), Superoxide Dismutase (SOD), Glutathione (GSH), and Angiotensin-converting enzyme (ACE) were determined by ELISA. Tumor necrosis factor-alpha (TNF-α) expression was described by RT-qPCR. Caspase-3 immunostaining was performed to evaluate apoptosis. Compared with the model group, a significant decrease was observed in the MPO, IL-8, MAPK, ACE, LPO levels, and TNF-α expression in the ARDS+ Hispidulin group. Moreover, reduced caspase-3 immunoreactivity and activity of ACE were detected in the Hispidulin+ARDS group. The protective effect of Hispidulin treatment may act through inhibition of the ACE activity and then regulation of inflammatory cytokine level and alteration of apoptosis. © 2023 Informa UK Limited, trading as Taylor & Francis Group.
dc.description.sponsorshipThis work was supported by the BAP from Atatürk University (grant number FKP-2021-8719)
dc.identifier.doi10.1080/09603123.2023.2166023
dc.identifier.eissn1369-1619
dc.identifier.endpage766
dc.identifier.issn0960-3123
dc.identifier.issue2
dc.identifier.pmid36624973
dc.identifier.scopus2-s2.0-85146245117
dc.identifier.startpage755
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11537
dc.identifier.volume34
dc.identifier.wosWOS:000909864500001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofInternational Journal of Environmental Health Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectACE activity
dc.subjectHispidulin
dc.subjectlung injury with ARDS
dc.subjectAnimals
dc.subjectCaspase 3
dc.subjectFlavones
dc.subjectInterleukin-8
dc.subjectLung
dc.subjectMitogen-Activated Protein Kinases
dc.subjectOleic Acid
dc.subjectRats
dc.subjectRespiratory Distress Syndrome
dc.subjectTumor Necrosis Factor-alpha
dc.subjectdipeptidyl carboxypeptidase
dc.subjectglutathione
dc.subjectinterleukin 8
dc.subjectmitogen activated protein kinase
dc.subjectmyeloperoxidase
dc.subjectsuperoxide dismutase
dc.subjecttumor necrosis factor
dc.subjectflavone derivative
dc.subjectapoptosis
dc.subjectcell
dc.subjectenzyme
dc.subjectenzyme activity
dc.subjectfatty acid
dc.subjectgene expression
dc.subjectinhibition
dc.subjectinjury
dc.subjectorganic compound
dc.titleHispidulin exerts a protective effect against oleic acid induced-ARDS in the rat via inhibition of ACE activity and MAPK pathway
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus5
rdl.citation.wos4
rdl.departmentDepartment of Histology and Embryology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)