Protective effect of astaxanthin and metformin in the liver of rats in which the polycystic ovary syndrome model was formed by giving letrozole

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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.

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AlanDeğerDil
dc.contributor.authorTaştan, Tuǧba Bal
dc.contributor.authorAkaras, Nurhan
dc.contributor.authorDemir, Özlem
dc.contributor.authorUgan, Rüstem Anil
dc.date.accessioned2026-10-18T20:27:04.039189694Z
dc.date.available2026-10-18T20:27:04.039189694Z
dc.date.issued2023
dc.description.abstractObjective(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.doi10.22038/ijbms.2023.68032.14872
dc.identifier.eissn2008-3874
dc.identifier.endpage694
dc.identifier.issn2008-3866
dc.identifier.issue6
dc.identifier.pmcidPMC10237172
dc.identifier.pmid37275752
dc.identifier.scopus2-s2.0-85162861692
dc.identifier.startpage688
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12119
dc.identifier.volume26
dc.identifier.wosWOS:000988782100010
dc.language.isoen
dc.publisherMashhad University of Medical Sciences
dc.relation.ispartofIranian Journal of Basic Medical Sciences
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAstaxanthine
dc.subjectLiver
dc.subjectMetformin
dc.subjectOxidative stress
dc.subjectPolycystic ovary syndrome
dc.subjectRat
dc.subjectastaxanthin
dc.subjectcaspase 3
dc.subjecteosin
dc.subjecthematoxylin
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectletrozole
dc.subjectmalonaldehyde
dc.subjectsuperoxide dismutase
dc.subjectadult
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectfemale
dc.subjecthistology
dc.subjectimmunohistochemistry
dc.subjectliver cell
dc.subjectliver protection
dc.subjectnonhuman
dc.subjectovary polycystic disease
dc.titleProtective effect of astaxanthin and metformin in the liver of rats in which the polycystic ovary syndrome model was formed by giving letrozole
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus21
rdl.citation.wos19
rdl.departmentDepartment of Histology and Embryology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)