Hispidulin exerts a protective effect against oleic acid induced-ARDS in the rat via inhibition of ACE activity and MAPK pathway
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.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Koc, Kubra | |
| dc.contributor.author | Ozek, Nihal Simsek | |
| dc.contributor.author | Aysin, Ferhunde | |
| dc.contributor.author | Demir, Ozlem | |
| dc.contributor.author | Yilmaz, Asli | |
| dc.contributor.author | Yilmaz, Mehmet | |
| dc.contributor.author | Geyikoglu, Fatime | |
| dc.contributor.author | Erol, Huseyin Serkan | |
| dc.date.accessioned | 2026-10-18T20:26:34.445960284Z | |
| dc.date.available | 2026-10-18T20:26:34.445960284Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | This work was supported by the BAP from Atatürk University (grant number FKP-2021-8719) | |
| dc.identifier.doi | 10.1080/09603123.2023.2166023 | |
| dc.identifier.eissn | 1369-1619 | |
| dc.identifier.endpage | 766 | |
| dc.identifier.issn | 0960-3123 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 36624973 | |
| dc.identifier.scopus | 2-s2.0-85146245117 | |
| dc.identifier.startpage | 755 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/11537 | |
| dc.identifier.volume | 34 | |
| dc.identifier.wos | WOS:000909864500001 | |
| dc.language.iso | en | |
| dc.publisher | Taylor and Francis Ltd. | |
| dc.relation.ispartof | International Journal of Environmental Health Research | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | ACE activity | |
| dc.subject | Hispidulin | |
| dc.subject | lung injury with ARDS | |
| dc.subject | Animals | |
| dc.subject | Caspase 3 | |
| dc.subject | Flavones | |
| dc.subject | Interleukin-8 | |
| dc.subject | Lung | |
| dc.subject | Mitogen-Activated Protein Kinases | |
| dc.subject | Oleic Acid | |
| dc.subject | Rats | |
| dc.subject | Respiratory Distress Syndrome | |
| dc.subject | Tumor Necrosis Factor-alpha | |
| dc.subject | dipeptidyl carboxypeptidase | |
| dc.subject | glutathione | |
| dc.subject | interleukin 8 | |
| dc.subject | mitogen activated protein kinase | |
| dc.subject | myeloperoxidase | |
| dc.subject | superoxide dismutase | |
| dc.subject | tumor necrosis factor | |
| dc.subject | flavone derivative | |
| dc.subject | apoptosis | |
| dc.subject | cell | |
| dc.subject | enzyme | |
| dc.subject | enzyme activity | |
| dc.subject | fatty acid | |
| dc.subject | gene expression | |
| dc.subject | inhibition | |
| dc.subject | injury | |
| dc.subject | organic compound | |
| dc.title | Hispidulin exerts a protective effect against oleic acid induced-ARDS in the rat via inhibition of ACE activity and MAPK pathway | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 5 | |
| rdl.citation.wos | 4 | |
| rdl.department | Department of Histology and Embryology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
