Comparative study of the protective effects of adenosine triphosphate and resveratrol against amiodarone-induced potential liver damage and dysfunction in rats

ArticleAçık Erişim

Özet

Background. Amiodarone is the most commonly used class III antiarrhythmic drug with antiarrhythmic and vasodilator properties. Adenosine triphosphate (ATP) serves as a crucial source of intracellular energy, while resveratrol is known for its potent antioxidant activity. Objectives. This study aimed to biochemically, histopathologically and immunohistochemically evaluate the effects of ATP, resveratrol and their combination on potential liver damage and dysfunction induced by amiodarone in rats. Materials and methods. The rats were divided into 6 groups: healthy control (HG), amiodarone alone (ADG), amiodarone + ATP at 2 mg/kg (AAG-2), amiodarone + ATP at 5 mg/kg (AAG-5), resveratrol + amiodarone (RAG), and resveratrol + amiodarone + ATP at 2 mg/kg (RAA-2). Amiodarone (50 mg/kg, orally), ATP (2 mg/kg and 5 mg/kg, intraperitoneally) and resveratrol (25 mg/kg, orally) were administered once daily for 14 days. Following treatment, liver tissues were excised for biochemical analysis. Oxidative stress was assessed by measuring malondialdehyde (MDA) levels, while antioxidant status was evaluated through total glutathione (GSH), superoxide dismutase (SOD) and catalase (CAT) levels. To assess liver function, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities were measured in serum samples collected from the animals’ tail veins. In addition, liver tissues were subjected to histopathological and immunohistochemical examination to evaluate structural and molecular changes associated with treatment. Results. Amiodarone administration led to a significant increase in oxidative stress markers and a reduction in antioxidant levels in rat liver tissue. Additionally, serum levels of ALT and AST were elevated, indicating liver dysfunction. Histopathological and immunohistochemical analyses revealed severe (grade 3) oxidative damage in the liver tissue. All biochemical parameters in the 5 mg/kg ATP and resveratrol + 2 mg/kg ATP treatment groups were comparable to those observed in the HG group. Histopathological and immunohistochemical evaluations showed a reduction in liver damage severity to grade 2 in the groups treated with ATP (2 mg/kg) and resveratrol alone, and to grade 1 in the groups receiving ATP (5 mg/kg) or the combination of resveratrol + ATP (2 mg/kg). Conclusions. The results of the present study suggest that adjusting the ATP dosage or using a combination of ATP and resveratrol may be effective strategies for minimizing amiodarone-induced liver damage. © Copyright by Author(s). This is an article distributed under the terms of the Creative Commons Attribution 3.0 Unported (CC BY 3.0) (https://creativecommons.org/licenses/by/3.0/)

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13833Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17219/acem/202011Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKaradogan, Muhammed Talha
dc.contributor.authorYavuzer, Bulent
dc.contributor.authorGursul, Cebrail
dc.contributor.authorHuseynova, Gulbaniz
dc.contributor.authorYazici, Gulce Naz
dc.contributor.authorGulaboglu, Mine
dc.contributor.authorYilmaz, Furkan
dc.contributor.authorMendil, Ali Sefa
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:28:38.373090382Z
dc.date.available2026-10-18T20:28:38.373090382Z
dc.date.issued2020
dc.description.abstractBackground. Amiodarone is the most commonly used class III antiarrhythmic drug with antiarrhythmic and vasodilator properties. Adenosine triphosphate (ATP) serves as a crucial source of intracellular energy, while resveratrol is known for its potent antioxidant activity. Objectives. This study aimed to biochemically, histopathologically and immunohistochemically evaluate the effects of ATP, resveratrol and their combination on potential liver damage and dysfunction induced by amiodarone in rats. Materials and methods. The rats were divided into 6 groups: healthy control (HG), amiodarone alone (ADG), amiodarone + ATP at 2 mg/kg (AAG-2), amiodarone + ATP at 5 mg/kg (AAG-5), resveratrol + amiodarone (RAG), and resveratrol + amiodarone + ATP at 2 mg/kg (RAA-2). Amiodarone (50 mg/kg, orally), ATP (2 mg/kg and 5 mg/kg, intraperitoneally) and resveratrol (25 mg/kg, orally) were administered once daily for 14 days. Following treatment, liver tissues were excised for biochemical analysis. Oxidative stress was assessed by measuring malondialdehyde (MDA) levels, while antioxidant status was evaluated through total glutathione (GSH), superoxide dismutase (SOD) and catalase (CAT) levels. To assess liver function, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities were measured in serum samples collected from the animals’ tail veins. In addition, liver tissues were subjected to histopathological and immunohistochemical examination to evaluate structural and molecular changes associated with treatment. Results. Amiodarone administration led to a significant increase in oxidative stress markers and a reduction in antioxidant levels in rat liver tissue. Additionally, serum levels of ALT and AST were elevated, indicating liver dysfunction. Histopathological and immunohistochemical analyses revealed severe (grade 3) oxidative damage in the liver tissue. All biochemical parameters in the 5 mg/kg ATP and resveratrol + 2 mg/kg ATP treatment groups were comparable to those observed in the HG group. Histopathological and immunohistochemical evaluations showed a reduction in liver damage severity to grade 2 in the groups treated with ATP (2 mg/kg) and resveratrol alone, and to grade 1 in the groups receiving ATP (5 mg/kg) or the combination of resveratrol + ATP (2 mg/kg). Conclusions. The results of the present study suggest that adjusting the ATP dosage or using a combination of ATP and resveratrol may be effective strategies for minimizing amiodarone-induced liver damage. © Copyright by Author(s). This is an article distributed under the terms of the Creative Commons Attribution 3.0 Unported (CC BY 3.0) (https://creativecommons.org/licenses/by/3.0/)
dc.identifier.doi10.17219/acem/202011
dc.identifier.eissn2451-2680
dc.identifier.endpage2152
dc.identifier.issn1899-5276
dc.identifier.issue12
dc.identifier.pmid40827931
dc.identifier.scopus2-s2.0-105025145600
dc.identifier.startpage2137
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13833
dc.identifier.volume34
dc.identifier.wosWOS:001553540800001
dc.language.isoen
dc.publisherWroclaw Medical University
dc.relation.ispartofAdvances in Clinical and Experimental Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectadenosine triphosphate
dc.subjectamiodarone
dc.subjectoxidative liver damage
dc.subjectrats
dc.subjectresveratrol
dc.subjectAnimals
dc.subjectAnti-Arrhythmia Agents
dc.subjectAntioxidants
dc.subjectChemical and Drug Induced Liver Injury
dc.subjectLiver
dc.subjectMale
dc.subjectOxidative Stress
dc.subjectRats, Wistar
dc.subjectantiarrhythmic agent
dc.subjectantioxidant
dc.subjectanimal
dc.subjectcomparative study
dc.subjectdrug effect
dc.subjectmetabolism
dc.subjectpathology
dc.subjectprevention and control
dc.subjectrat
dc.subjectWistar rat
dc.titleComparative study of the protective effects of adenosine triphosphate and resveratrol against amiodarone-induced potential liver damage and dysfunction in rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus6
rdl.citation.wos6
rdl.departmentDepartment of Pediatrics, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Histology and Embryology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)