Protective effect of astaxanthin and metformin in the liver of rats in which the polycystic ovary syndrome model was formed by giving letrozole
Özet
Objective(s): In this study, the effects of astaxanthin on liver tissue in rats with polycystic ovary syndrome (PCOS) were evaluated. Materials and Methods: Fifty-four Spraque-Dawley rats were divided into 9 groups: Groups: Control, PCOS, PCOS+Metformin (Met), PCOS+ Astaxanthin (ASX)10, PCOS+ASX20, PCOS+ASX40, PCOS+Met+ASX10, PCOS+Met+ASX20, and PCOS+Met+ASX40. PCOS was induced in female rats by oral administration of letrozole (1 mg/kg) for 21 days. Rats were treated with ASX (10 mg/kg), ASX (20 mg/kg), ASX (40 mg/kg), and metformin (20 mg/kg) for 7 days after PCOS induction. At the end of the experiment, malondialdehyde (MDA) and superoxide dismutase (SOD) levels were measured in the liver tissue. The liver was stained with hematoxylin/eosin for histological examination. Additionally, NF-kB and caspase 3 were analyzed immunohistochemically. Results: A remarkable abnormality was observed in the biochemical and histological parameters in the liver tissue of the PCOS model rats. Astaxanthin dose-dependently normalized the MDA level. Additionally, astaxanthin showed a protective effect by increasing the SOD level and increasing its antioxidant activities. We observed that administration of astaxanthin in addition to metformin applied in the standard was more effective. Caspase 3 and NF-kB immune positivity was lower in the groups given astaxanthin compared with PCOS. Histologically, it was observed that astaxanthin improved the deteriorated liver morphology in the letrozole-induced PCOS group. Conclusion: According to our results, it was observed that astaxanthin had antioxidant, anti-inflammatory and anti-apoptotic effects on PCOS in the treatment groups. Therefore, it was concluded that astaxanthin may have a protective effect against PCOS side effects. © 2023 Mashhad University of Medical Sciences. All rights reserved.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Taştan, Tuǧba Bal | |
| dc.contributor.author | Akaras, Nurhan | |
| dc.contributor.author | Demir, Özlem | |
| dc.contributor.author | Ugan, Rüstem Anil | |
| dc.date.accessioned | 2026-10-18T20:27:04.039189694Z | |
| dc.date.available | 2026-10-18T20:27:04.039189694Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Objective(s): In this study, the effects of astaxanthin on liver tissue in rats with polycystic ovary syndrome (PCOS) were evaluated. Materials and Methods: Fifty-four Spraque-Dawley rats were divided into 9 groups: Groups: Control, PCOS, PCOS+Metformin (Met), PCOS+ Astaxanthin (ASX)10, PCOS+ASX20, PCOS+ASX40, PCOS+Met+ASX10, PCOS+Met+ASX20, and PCOS+Met+ASX40. PCOS was induced in female rats by oral administration of letrozole (1 mg/kg) for 21 days. Rats were treated with ASX (10 mg/kg), ASX (20 mg/kg), ASX (40 mg/kg), and metformin (20 mg/kg) for 7 days after PCOS induction. At the end of the experiment, malondialdehyde (MDA) and superoxide dismutase (SOD) levels were measured in the liver tissue. The liver was stained with hematoxylin/eosin for histological examination. Additionally, NF-kB and caspase 3 were analyzed immunohistochemically. Results: A remarkable abnormality was observed in the biochemical and histological parameters in the liver tissue of the PCOS model rats. Astaxanthin dose-dependently normalized the MDA level. Additionally, astaxanthin showed a protective effect by increasing the SOD level and increasing its antioxidant activities. We observed that administration of astaxanthin in addition to metformin applied in the standard was more effective. Caspase 3 and NF-kB immune positivity was lower in the groups given astaxanthin compared with PCOS. Histologically, it was observed that astaxanthin improved the deteriorated liver morphology in the letrozole-induced PCOS group. Conclusion: According to our results, it was observed that astaxanthin had antioxidant, anti-inflammatory and anti-apoptotic effects on PCOS in the treatment groups. Therefore, it was concluded that astaxanthin may have a protective effect against PCOS side effects. © 2023 Mashhad University of Medical Sciences. All rights reserved. | |
| dc.identifier.doi | 10.22038/ijbms.2023.68032.14872 | |
| dc.identifier.eissn | 2008-3874 | |
| dc.identifier.endpage | 694 | |
| dc.identifier.issn | 2008-3866 | |
| dc.identifier.issue | 6 | |
| dc.identifier.pmcid | PMC10237172 | |
| dc.identifier.pmid | 37275752 | |
| dc.identifier.scopus | 2-s2.0-85162861692 | |
| dc.identifier.startpage | 688 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12119 | |
| dc.identifier.volume | 26 | |
| dc.identifier.wos | WOS:000988782100010 | |
| dc.language.iso | en | |
| dc.publisher | Mashhad University of Medical Sciences | |
| dc.relation.ispartof | Iranian Journal of Basic Medical Sciences | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Astaxanthine | |
| dc.subject | Liver | |
| dc.subject | Metformin | |
| dc.subject | Oxidative stress | |
| dc.subject | Polycystic ovary syndrome | |
| dc.subject | Rat | |
| dc.subject | astaxanthin | |
| dc.subject | caspase 3 | |
| dc.subject | eosin | |
| dc.subject | hematoxylin | |
| dc.subject | immunoglobulin enhancer binding protein | |
| dc.subject | letrozole | |
| dc.subject | malonaldehyde | |
| dc.subject | superoxide dismutase | |
| dc.subject | adult | |
| dc.subject | animal cell | |
| dc.subject | animal experiment | |
| dc.subject | animal model | |
| dc.subject | animal tissue | |
| dc.subject | antioxidant activity | |
| dc.subject | Article | |
| dc.subject | female | |
| dc.subject | histology | |
| dc.subject | immunohistochemistry | |
| dc.subject | liver cell | |
| dc.subject | liver protection | |
| dc.subject | nonhuman | |
| dc.subject | ovary polycystic disease | |
| dc.title | Protective effect of astaxanthin and metformin in the liver of rats in which the polycystic ovary syndrome model was formed by giving letrozole | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 21 | |
| rdl.citation.wos | 19 | |
| 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) |
