Astaxanthin treatment reduces kidney damage and facilitates antioxidant recovery in lithium-intoxicated rats

ArticleAçık Erişim

Özet

Objective: This study aimed to evaluate the protective effects of astaxanthin against lithium-induced nephrotoxicity, focusing on histopathological changes, oxidative stress modulation, and alteration in the expression of key proteins related to apoptosis and inflammation. Methods: In this study, 56 male rats were utilized and divided into experimental groups subjected to lithium-induced nephrotoxicity, with and without astaxanthin treatment, over 14 and 28 days. The parameters assessed included oxidative stress markers (MDA, GSH, SOD), protein expression levels of BCL-2, BAX, TNF- α, PI3K, NF-κ B-p65, IL-1β, and comprehensive histopathological examinations to evaluate the integrity of renal tissue. Results: Lithium exposure led to significant renal damage, as evidenced by histological distortions in renal architecture, increased oxidative stress indicated by elevated MDA levels, and dysregulated expressions of apoptotic and inflammatory proteins. Notably, histopathological analysis revealed glomerular and tubular degeneration in lithium-treated groups. Astaxanthin treatment effectively mitigated these effects, demonstrating its efficacy in reducing lipid peroxidation, rebalancing apoptotic proteins, suppressing pro-inflammatory cytokines, and preserving renal histological structure. The concurrent use of lithium and astaxanthin showed a considerable amelioration of lithium-induced damage, suggesting astaxanthin's role in attenuating the nephrotoxic effects of lithium, both at a molecular and structural level. Conclusion: Astaxanthin demonstrates significant renoprotective effects against lithium-induced nephrotoxicity, suggesting its utility as an effective adjunctive therapy. Through its potent antioxidative, anti-inflammatory, and anti-apoptotic actions, astaxanthin effectively reduces renal damage associated with lithium treatment, underscoring its potential for enhancing renal health in patients receiving lithium therapy. © 2024 Elsevier Ltd

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11867Resmi atıflarda kullanılan kalıcı adres
Tam Kayıt
AlanDeğerDil
dc.contributor.authorErbaş, Elif
dc.contributor.authorÜstündağ, Hilal
dc.contributor.authorÖztürk, Emre
dc.contributor.authorParlak, Seçil Nazife
dc.contributor.authorAtcalı, Tuğçe
dc.date.accessioned2026-10-18T20:26:51.603627523Z
dc.date.available2026-10-18T20:26:51.603627523Z
dc.date.issued2024
dc.description.abstractObjective: This study aimed to evaluate the protective effects of astaxanthin against lithium-induced nephrotoxicity, focusing on histopathological changes, oxidative stress modulation, and alteration in the expression of key proteins related to apoptosis and inflammation. Methods: In this study, 56 male rats were utilized and divided into experimental groups subjected to lithium-induced nephrotoxicity, with and without astaxanthin treatment, over 14 and 28 days. The parameters assessed included oxidative stress markers (MDA, GSH, SOD), protein expression levels of BCL-2, BAX, TNF- α, PI3K, NF-κ B-p65, IL-1β, and comprehensive histopathological examinations to evaluate the integrity of renal tissue. Results: Lithium exposure led to significant renal damage, as evidenced by histological distortions in renal architecture, increased oxidative stress indicated by elevated MDA levels, and dysregulated expressions of apoptotic and inflammatory proteins. Notably, histopathological analysis revealed glomerular and tubular degeneration in lithium-treated groups. Astaxanthin treatment effectively mitigated these effects, demonstrating its efficacy in reducing lipid peroxidation, rebalancing apoptotic proteins, suppressing pro-inflammatory cytokines, and preserving renal histological structure. The concurrent use of lithium and astaxanthin showed a considerable amelioration of lithium-induced damage, suggesting astaxanthin's role in attenuating the nephrotoxic effects of lithium, both at a molecular and structural level. Conclusion: Astaxanthin demonstrates significant renoprotective effects against lithium-induced nephrotoxicity, suggesting its utility as an effective adjunctive therapy. Through its potent antioxidative, anti-inflammatory, and anti-apoptotic actions, astaxanthin effectively reduces renal damage associated with lithium treatment, underscoring its potential for enhancing renal health in patients receiving lithium therapy. © 2024 Elsevier Ltd
dc.identifier.doi10.1016/j.toxicon.2024.107664
dc.identifier.eissn1879-3150
dc.identifier.issn0041-0101
dc.identifier.pmid38460603
dc.identifier.scopus2-s2.0-85187943453
dc.identifier.startpage107664
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11867
dc.identifier.volume241
dc.identifier.wosWOS:001206485200001
dc.language.isoen
dc.publisherElsevier Ltd
dc.relation.ispartofToxicon
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectApoptosis
dc.subjectAstaxanthin
dc.subjectLithium
dc.subjectNephrotoxicity
dc.subjectOxidative stress
dc.subjectRenal protection
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectHumans
dc.subjectKidney
dc.subjectKidney Diseases
dc.subjectMale
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectXanthophylls
dc.subject3,4 methylenedioxyamphetamine
dc.subjectglutathione
dc.subjectI kappa B kinase gamma
dc.subjectinterleukin 1
dc.subjectprotein Bax
dc.subjectprotein bcl 2
dc.subjecttumor necrosis factor
dc.subjectantioxidant
dc.subjectxanthophyll
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectcontrolled study
dc.titleAstaxanthin treatment reduces kidney damage and facilitates antioxidant recovery in lithium-intoxicated rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus28
rdl.citation.wos24
rdl.departmentErzincan Binali Yıldırım University, Faculty of Medicine, Department of Physiology, Erzincan, Turkiye. Electronic address: hilal.ustundag@erzincan.edu.tr.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)