Effects of Achillea millefolium on cisplatin induced ocular toxicity: an experimental study

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Aim: Cisplatin is a widely used and highly effective anti-cancer agent and one of the limiting side effects of cisplatin is ocular toxicity. Achillea millefolium, also known as yarrow, is a plant that has been used for many years to treat various health problems including chemotherapy-related toxicities. Methods: The present investigation was designed to evaluate the biochemical, molecular and histopathological effects of Achillea Millefolium on cisplatin-induced oxidative and inflammatory ocular damage in rats. Twenty-four adult male rats were assigned randomly to four groups (n = 6) as (1) control, (2) cisplatin (7 mg/kg, intraperitoneally), (3) Cisplatin + Achillea millefolium (200 mg/kg, orally for 14 consecutive days), (4) Cisplatin + Achillea millefolium (400 mg/kg, orally for 14 consecutive days). Levels of total antioxidant capacity and total oxidant status, SOD, MDA, IL-1β, and IL-10 were measured in ocular tissue. The mRNA expressions of TNF-α, nuclear factor kappa B and Caspase-3 were evaluated. Also, ocular sections were evaluated histopathologically. Results: Achillea Millefolium upregulated ocular antioxidant enzymes and downregulated inflammation. The SOD activity and total antioxidant capacity increased whereas total oxidant status and MDA levels decreased significantly at high dose group. High dose Achillea millefolium treatment reduced the IL-1β concentrations, whereas IL-10 levels increased significantly in that group. Moreover, we observed that Achillea millefolium restored ocular histopathological structure and significantly suppressed apoptosis by reducing the expression of Caspase-3. Conclusion: Collectively, our results suggest that Achillea millefolium have protective effects against cisplatin-induced ocular toxicity and is a promising adjuvant therapy with the potential to prevent cisplatin related ocular toxicity. © 2021 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorOkkay, Ufuk
dc.contributor.authorFerah Okkay, Irmak
dc.contributor.authorAydin, Ismail Cagri
dc.contributor.authorBayram, Cemil
dc.contributor.authorErtugrul, Muhammed Sait
dc.contributor.authorGezer, Arzu
dc.contributor.authorHacimuftuoglu, Ahmet
dc.date.accessioned2026-10-18T20:27:51.506579502Z
dc.date.available2026-10-18T20:27:51.506579502Z
dc.date.issued2021
dc.description.abstractAim: Cisplatin is a widely used and highly effective anti-cancer agent and one of the limiting side effects of cisplatin is ocular toxicity. Achillea millefolium, also known as yarrow, is a plant that has been used for many years to treat various health problems including chemotherapy-related toxicities. Methods: The present investigation was designed to evaluate the biochemical, molecular and histopathological effects of Achillea Millefolium on cisplatin-induced oxidative and inflammatory ocular damage in rats. Twenty-four adult male rats were assigned randomly to four groups (n = 6) as (1) control, (2) cisplatin (7 mg/kg, intraperitoneally), (3) Cisplatin + Achillea millefolium (200 mg/kg, orally for 14 consecutive days), (4) Cisplatin + Achillea millefolium (400 mg/kg, orally for 14 consecutive days). Levels of total antioxidant capacity and total oxidant status, SOD, MDA, IL-1β, and IL-10 were measured in ocular tissue. The mRNA expressions of TNF-α, nuclear factor kappa B and Caspase-3 were evaluated. Also, ocular sections were evaluated histopathologically. Results: Achillea Millefolium upregulated ocular antioxidant enzymes and downregulated inflammation. The SOD activity and total antioxidant capacity increased whereas total oxidant status and MDA levels decreased significantly at high dose group. High dose Achillea millefolium treatment reduced the IL-1β concentrations, whereas IL-10 levels increased significantly in that group. Moreover, we observed that Achillea millefolium restored ocular histopathological structure and significantly suppressed apoptosis by reducing the expression of Caspase-3. Conclusion: Collectively, our results suggest that Achillea millefolium have protective effects against cisplatin-induced ocular toxicity and is a promising adjuvant therapy with the potential to prevent cisplatin related ocular toxicity. © 2021 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doi10.1080/15569527.2021.1919137
dc.identifier.eissn1556-9535
dc.identifier.endpage220
dc.identifier.issn1556-9527
dc.identifier.issue3
dc.identifier.pmid34180746
dc.identifier.scopus2-s2.0-85114058064
dc.identifier.startpage214
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13009
dc.identifier.volume40
dc.identifier.wosWOS:000667538700001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofCutaneous and Ocular Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAchillea millefolium
dc.subjectapoptosis
dc.subjectcisplatin
dc.subjectinflammation
dc.subjectocular toxicity
dc.subjectoxidative stress
dc.subjectrat
dc.subjectAchillea
dc.subjectAdministration, Oral
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectCornea
dc.subjectCorneal Diseases
dc.subjectDisease Models, Animal
dc.subjectDose-Response Relationship, Drug
dc.subjectHumans
dc.subjectMale
dc.subjectPlant Extracts
dc.subjectRats
dc.subjectAchillea millefolium extract
dc.subjectcaspase 3
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectinterleukin 10
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectsuperoxide dismutase
dc.subjectthiopental
dc.subjecttumor necrosis factor
dc.subjectantioxidant
dc.subjectplant extract
dc.titleEffects of Achillea millefolium on cisplatin induced ocular toxicity: an experimental study
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus27
rdl.citation.wos22
rdl.departmentDepartment of Pharmacology, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan, Turkey.
rdl.oa.statusgreen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)