C entella asiatica extract protects against cisplatin-induced hepatotoxicity via targeting oxidative stress, inflammation, and apoptosis
Özet
This study was designed to investigate the protective effects of Centella asiatica (CA) on cisplatin-induced hepatotoxicity and to clarify the underlying mechanism by biochemical, molecular, immunohistochemical, and histopathological analyses. Rats were pre-treated with two doses of CA (100 and 200 mg/kg, p.o.) for 14 consecutive days. Then, on the 15th day, hepatotoxicity was induced by a single cisplatin injection (10 mg/kg i.p.). On the 18th day, the rats were euthanized. CA effectively alleviated cisplatin-induced hepatic injury via reduction in AST, ALT, and ALP enzymes and a decrease in oxidative stress (decreased MDA and ROS, and increased SOD, CAT, and GSH). CA also mitigated the inflammatory damage by the inhibition of TNF-α, IL-1β, and NF-κB. The liver expression of caspase-3 and Bax was downregulated, while Bcl-2 was upregulated. Moreover, immunohistochemical results confirmed the recovery with CA by downregulation of iNOS and 8-OHdG expression. These results showed that with its antioxidant, anti-inflammatory, and anti-apoptotic activities, CA could help alleviate the hepatotoxic effects of cisplatin chemotherapy. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Ferah Okkay, Irmak | |
| dc.contributor.author | Okkay, Ufuk | |
| dc.contributor.author | Aydin, Ismail Cagri | |
| dc.contributor.author | Bayram, Cemil | |
| dc.contributor.author | Ertugrul, Muhammed Sait | |
| dc.contributor.author | Mendil, Ali Sefa | |
| dc.contributor.author | Hacimuftuoglu, Ahmet | |
| dc.date.accessioned | 2026-10-18T20:27:31.346918900Z | |
| dc.date.available | 2026-10-18T20:27:31.346918900Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | This study was designed to investigate the protective effects of Centella asiatica (CA) on cisplatin-induced hepatotoxicity and to clarify the underlying mechanism by biochemical, molecular, immunohistochemical, and histopathological analyses. Rats were pre-treated with two doses of CA (100 and 200 mg/kg, p.o.) for 14 consecutive days. Then, on the 15th day, hepatotoxicity was induced by a single cisplatin injection (10 mg/kg i.p.). On the 18th day, the rats were euthanized. CA effectively alleviated cisplatin-induced hepatic injury via reduction in AST, ALT, and ALP enzymes and a decrease in oxidative stress (decreased MDA and ROS, and increased SOD, CAT, and GSH). CA also mitigated the inflammatory damage by the inhibition of TNF-α, IL-1β, and NF-κB. The liver expression of caspase-3 and Bax was downregulated, while Bcl-2 was upregulated. Moreover, immunohistochemical results confirmed the recovery with CA by downregulation of iNOS and 8-OHdG expression. These results showed that with its antioxidant, anti-inflammatory, and anti-apoptotic activities, CA could help alleviate the hepatotoxic effects of cisplatin chemotherapy. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. | |
| dc.identifier.doi | 10.1007/s11356-022-18626-z | |
| dc.identifier.eissn | 1614-7499 | |
| dc.identifier.endpage | 33784 | |
| dc.identifier.issn | 0944-1344 | |
| dc.identifier.issue | 22 | |
| dc.identifier.pmid | 35029831 | |
| dc.identifier.scopus | 2-s2.0-85123090820 | |
| dc.identifier.startpage | 33774 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12644 | |
| dc.identifier.volume | 29 | |
| dc.identifier.wos | WOS:000742623900004 | |
| dc.language.iso | en | |
| dc.publisher | Springer Science and Business Media Deutschland GmbH | |
| dc.relation.ispartof | Environmental Science and Pollution Research | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Apoptosis | |
| dc.subject | Centella asiatica | |
| dc.subject | Cisplatin | |
| dc.subject | Hepatotoxicity | |
| dc.subject | Inflammation | |
| dc.subject | Oxidative stress | |
| dc.subject | Animals | |
| dc.subject | Antioxidants | |
| dc.subject | Centella | |
| dc.subject | Chemical and Drug Induced Liver Injury | |
| dc.subject | Liver | |
| dc.subject | Plant Extracts | |
| dc.subject | Rats | |
| dc.subject | Triterpenes | |
| dc.subject | antioxidant | |
| dc.subject | Centella asiatica extract | |
| dc.subject | plant extract | |
| dc.subject | triterpene | |
| dc.subject | herb | |
| dc.subject | histopathology | |
| dc.subject | induced response | |
| dc.subject | inhibition | |
| dc.subject | injury | |
| dc.subject | toxicity | |
| dc.subject | animal | |
| dc.subject | metabolism | |
| dc.subject | rat | |
| dc.subject | toxic hepatitis | |
| dc.title | C entella asiatica extract protects against cisplatin-induced hepatotoxicity via targeting oxidative stress, inflammation, and apoptosis | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 24 | |
| rdl.citation.wos | 22 | |
| rdl.department | Department of Pharmacology, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan, Turkey. | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
