Suberosin Alleviates Sepsis-Induced Lung Injury in A Rat Model of Cecal Ligation and Puncture
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.
Anahtar Kelimeler
- Scopus
- 15
- WoS
- 11
- OpenAlex
- 15
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Karabulut Uzunçakmak, Sevgi | |
| dc.contributor.author | Halıcı, Zekai | |
| dc.contributor.author | Karakaya, Songül | |
| dc.contributor.author | Kutlu, Zerrin | |
| dc.contributor.author | Sağlam, Yavuz Selim | |
| dc.contributor.author | Bolat, İsmail | |
| dc.contributor.author | Aydın, Pelin | |
| dc.contributor.author | Kılıç, Ceyda Sibel | |
| dc.date.accessioned | 2026-10-29T19:08:54.305167511Z | |
| dc.date.available | 2026-10-29T19:08:54.305167511Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | 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. | |
| dc.identifier.doi | 10.1080/08941939.2022.2136802 | |
| dc.identifier.eissn | 1521-0553 | |
| dc.identifier.endpage | 9 | |
| dc.identifier.issn | 0894-1939 | |
| dc.identifier.issue | 1 | |
| dc.identifier.pmid | 36345760 | |
| dc.identifier.scopus | 2-s2.0-85141894711 | |
| dc.identifier.startpage | 1 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/bayburt/11870 | |
| dc.identifier.volume | 36 | |
| dc.identifier.wos | WOS:000879947700001 | |
| dc.language.iso | en | |
| dc.publisher | Taylor and Francis Ltd. | |
| dc.relation.ispartof | Journal of Investigative Surgery | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | lung injury | |
| dc.subject | oxidative stress | |
| dc.subject | rat | |
| dc.subject | sepsis | |
| dc.subject | suberosin | |
| dc.subject.classification | Surgery | |
| dc.subject.other | Animals | |
| dc.subject.other | Coumarins | |
| dc.subject.other | Disease Models, Animal | |
| dc.subject.other | Glutathione | |
| dc.subject.other | Ligation | |
| dc.subject.other | Lung | |
| dc.subject.other | Lung Injury | |
| dc.subject.other | Male | |
| dc.subject.other | Punctures | |
| dc.subject.other | Rats | |
| dc.subject.other | Rats, Wistar | |
| dc.subject.other | RNA, Messenger | |
| dc.subject.other | Sepsis | |
| dc.subject.other | Superoxide Dismutase | |
| dc.subject.other | Tumor Necrosis Factor-alpha | |
| dc.subject.other | adhesive agent | |
| dc.subject.other | antioxidant | |
| dc.subject.other | beta actin | |
| dc.subject.other | complementary DNA | |
| dc.subject.other | coumarin | |
| dc.subject.other | diaminobenzidine | |
| dc.subject.other | distilled water | |
| dc.subject.other | eosin | |
| dc.subject.other | formaldehyde | |
| dc.subject.other | hematoxylin | |
| dc.subject.other | interleukin 1beta | |
| dc.subject.other | ketamine | |
| dc.subject.other | malonaldehyde | |
| dc.subject.other | messenger RNA | |
| dc.subject.other | nuclease | |
| dc.subject.other | oxidizing agent | |
| dc.subject.other | paraffin | |
| dc.subject.other | peroxidase | |
| dc.subject.other | phosphate buffered saline | |
| dc.subject.other | protein | |
| dc.subject.other | sodium chloride | |
| dc.subject.other | suberosin | |
| dc.subject.other | tumor necrosis factor | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | xylazine | |
| dc.subject.other | xylene | |
| dc.subject.other | coumarin derivative | |
| dc.subject.other | abdominal cavity | |
| dc.subject.other | animal experiment | |
| dc.subject.other | animal model | |
| dc.subject.other | animal tissue | |
| dc.subject.other | antigen retrieval | |
| dc.subject.other | Apiaceae | |
| dc.subject.other | Article | |
| dc.subject.other | biochemical analysis | |
| dc.subject.other | body weight | |
| dc.subject.other | bronchiole | |
| dc.subject.other | bronchiole epithelium | |
| dc.subject.other | bronchus | |
| dc.subject.other | bronchus epithelium | |
| dc.subject.other | cecal ligation and puncture-induced sepsis | |
| dc.subject.other | cell infiltration | |
| dc.subject.other | controlled study | |
| dc.subject.other | degeneration | |
| dc.subject.other | desquamation | |
| dc.subject.other | drug effect | |
| dc.subject.other | enzyme activity | |
| dc.subject.other | enzyme linked immunosorbent assay | |
| dc.subject.other | epithelium | |
| dc.subject.other | Ferulago cassia | |
| dc.subject.other | gene expression profiling | |
| dc.subject.other | histopathology | |
| dc.subject.other | housekeeping gene | |
| dc.subject.other | incision | |
| dc.subject.other | inflammatory cell | |
| dc.subject.other | laparotomy | |
| dc.subject.other | light dark cycle | |
| dc.subject.other | lung alveolus wall | |
| dc.subject.other | lung parenchyma | |
| dc.subject.other | mononuclear cell | |
| dc.subject.other | mRNA expression level | |
| dc.subject.other | necrosis | |
| dc.subject.other | nonhuman | |
| dc.subject.other | oxidative stress | |
| dc.subject.other | perivascular cell | |
| dc.subject.other | protein expression | |
| dc.subject.other | rat | |
| dc.subject.other | real time polymerase chain reaction | |
| dc.subject.other | RNA extraction | |
| dc.subject.other | venous congestion | |
| dc.subject.other | adverse event | |
| dc.subject.other | animal | |
| dc.subject.other | complication | |
| dc.subject.other | disease model | |
| dc.subject.other | metabolism | |
| dc.subject.other | pathology | |
| dc.subject.other | puncture | |
| dc.subject.other | Wistar rat | |
| dc.title | Suberosin Alleviates Sepsis-Induced Lung Injury in A Rat Model of Cecal Ligation and Puncture | |
| dc.type | Article | |
| rdl.citation.openalex | 15 | |
| rdl.citation.scopus | 15 | |
| rdl.citation.wos | 11 | |
| rdl.department | Health Services Vocational School, Bayburt University, Bayburt, Turkey | |
| rdl.department | Department of Pharmacology, Faculty of Medicine, Atatürk University, Erzurum, Turkey | |
| rdl.department | Clinical Research, Development and Design Application and Research Center, Ataturk University, Erzurum, Turkey | |
| rdl.department | Department of Pharmaceutical Botany, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey | |
| rdl.department | Department of Biochemistry, Faculty of Pharmacy, Atatürk University, Erzurum, Turkey | |
| rdl.department | Department of Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey | |
| rdl.department | Department of Anesthesia, Regional Education and Research Hospital, Erzurum, Turkey | |
| rdl.department | Department of Pharmaceutical Botany, Faculty of Pharmacy, Ankara University, Ankara, Turkey | |
| rdl.oa.status | hybrid | |
| rdl.oa.url | https://doi.org/10.1080/08941939.2022.2136802 | |
| rdl.scopus.quartile | Q2 | |
| rdl.sdg | SDG03 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |

