Aprepitant: An antiemetic drug, contributes to the prevention of acute lung injury with its anti-inflammatory and antioxidant properties
Özet
Objectives: We investigated, the effects of aprepitant (APRE) on the lung tissues of rats with an experimental polymicrobial sepsis model (CLP: Cecal ligation and puncture) biochemically, molecularly and histopathologically. Methods: A total of 40 rats were divided into 5 groups with 8 animals in each group. Group 1 (SHAM), control group; Group 2 (CLP), cecal ligation and puncture; Group 3 (CLP + APRE10), rats were administered CLP + 10 mg/kg aprepitant; Group 4 (CLP + APRE20), rats were administered CLP + 20 mg/kg aprepitant; and Group 5 (CLP + APRE40), rats were administered CLP + 40 mg/kg aprepitant. A polymicrobial sepsis model was induced with CLP. After 16 h, lung tissues were taken for examination. Tumour necrosis factor α (TNF-α) and nuclear factor-kappa b (NFK-b) messenger ribonucleic acid (mRNA) expressions were analysed by real-time PCR (RT-PCR), biochemically antioxidant parameters such as superoxide dismutase (SOD) and glutathione (GSH) and oxidant parameters such as malondialdehyde (MDA) and lung damage histopathologically. Key findings and conclusions: The GSH level and SOD activity increased while the MDA level and the expressions of TNF-α and NFK-b were reduced in the groups treated with APRE, especially in the CLP + APRE40 group. The histopathology results supported the molecular and biochemical results. © The Author(s) 2021.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Kose, Duygu | |
| dc.contributor.author | Un, Harun | |
| dc.contributor.author | Ugan, Rustem Anil | |
| dc.contributor.author | Halici, Zekai | |
| dc.contributor.author | Cadirci, Elif | |
| dc.contributor.author | Tastan, Tugba Bal | |
| dc.contributor.author | Kahramanlar, Aysenur | |
| dc.date.accessioned | 2026-10-18T20:28:11.234003465Z | |
| dc.date.available | 2026-10-18T20:28:11.234003465Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | Objectives: We investigated, the effects of aprepitant (APRE) on the lung tissues of rats with an experimental polymicrobial sepsis model (CLP: Cecal ligation and puncture) biochemically, molecularly and histopathologically. Methods: A total of 40 rats were divided into 5 groups with 8 animals in each group. Group 1 (SHAM), control group; Group 2 (CLP), cecal ligation and puncture; Group 3 (CLP + APRE10), rats were administered CLP + 10 mg/kg aprepitant; Group 4 (CLP + APRE20), rats were administered CLP + 20 mg/kg aprepitant; and Group 5 (CLP + APRE40), rats were administered CLP + 40 mg/kg aprepitant. A polymicrobial sepsis model was induced with CLP. After 16 h, lung tissues were taken for examination. Tumour necrosis factor α (TNF-α) and nuclear factor-kappa b (NFK-b) messenger ribonucleic acid (mRNA) expressions were analysed by real-time PCR (RT-PCR), biochemically antioxidant parameters such as superoxide dismutase (SOD) and glutathione (GSH) and oxidant parameters such as malondialdehyde (MDA) and lung damage histopathologically. Key findings and conclusions: The GSH level and SOD activity increased while the MDA level and the expressions of TNF-α and NFK-b were reduced in the groups treated with APRE, especially in the CLP + APRE40 group. The histopathology results supported the molecular and biochemical results. © The Author(s) 2021. | |
| dc.identifier.doi | 10.1093/jpp/rgab088 | |
| dc.identifier.eissn | 2042-7158 | |
| dc.identifier.endpage | 1309 | |
| dc.identifier.issn | 0022-3573 | |
| dc.identifier.issue | 10 | |
| dc.identifier.pmid | 34160038 | |
| dc.identifier.scopus | 2-s2.0-85116957241 | |
| dc.identifier.startpage | 1302 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/13346 | |
| dc.identifier.volume | 73 | |
| dc.identifier.wos | WOS:000696581500003 | |
| dc.language.iso | en | |
| dc.publisher | Oxford University Press | |
| dc.relation.ispartof | Journal of Pharmacy and Pharmacology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Aprepitant | |
| dc.subject | Nuclear factor-kappa b | |
| dc.subject | Polymicrobial sepsis | |
| dc.subject | Tumour necrosis factor α | |
| dc.subject | Acute Lung Injury | |
| dc.subject | Animals | |
| dc.subject | Anti-Inflammatory Agents | |
| dc.subject | Antiemetics | |
| dc.subject | Antioxidants | |
| dc.subject | Cecum | |
| dc.subject | Disease Models, Animal | |
| dc.subject | Female | |
| dc.subject | Glutathione | |
| dc.subject | Inflammation | |
| dc.subject | Ligation | |
| dc.subject | Lung | |
| dc.subject | Malondialdehyde | |
| dc.subject | NF-kappa B | |
| dc.subject | Oxidative Stress | |
| dc.subject | Peroxidase | |
| dc.subject | Rats, Sprague-Dawley | |
| dc.subject | Sepsis | |
| dc.subject | Superoxide Dismutase | |
| dc.subject | Tumor Necrosis Factor-alpha | |
| dc.subject | immunoglobulin enhancer binding protein | |
| dc.subject | malonaldehyde | |
| dc.subject | messenger RNA | |
| dc.subject | tumor necrosis factor | |
| dc.subject | antiemetic agent | |
| dc.subject | antiinflammatory agent | |
| dc.title | Aprepitant: An antiemetic drug, contributes to the prevention of acute lung injury with its anti-inflammatory and antioxidant properties | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 18 | |
| rdl.citation.wos | 18 | |
| rdl.oa.status | green | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
