Effects of ketamine, thiopental and their combination on the rat liver: A biochemical evaluation

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Özet

Background. In the literature, it has been suggested that ketamine-related oxidative organ damage results from increased blood adrenaline level, and thiopental-related oxidative damage is caused by decreased adrenaline level, suggesting that ketamine-thiopental combination (KT) may be beneficial in reducing the hepatotoxic effect of ketamine. Objectives. To biochemically investigate the effects of ketamine, thiopental and KT on the liver in rats. Materials and methods. Male albino Wistar type rats received intraperitoneally (ip.) 30 mg/kg ketamine in the ketamine alone (KG) group (n = 6), 15 mg/kg thiopental in the thiopental alone (TG) group (n = 6), and 30 mg/kg ketamine + 15 mg/kg thiopental in the ketamine+thiopental (KTG) group (n = 6). The same volume of distilled water as solvent was given to the healthy (HG) animal group. This procedure was repeated once daily for 30 days. At the end of this period, the animals were killed by decapitation and their livers were removed. In liver tissue, malondialdehyde (MDA), total glutathione (tGSH), total oxidant status (TOS), total antioxidant status (TAS), tumor necrosis factor alpha (TNF-α), interleukin 1 beta (IL-1β), and interleukin-6 (IL-6) levels were measured. The IL-1β, IL-6, TNF-α, adrenalin (ADR), noradrenalin (NDR), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) levels were determined in blood samples taken from the tail veins. Results. In the group treated with ketamine and thiopental alone, MDA, TOS, IL-1β, IL-6, TNF-α, ADR, NDR, ALT, and AST levels were found to be high, and those of tGSH and TAS to be low. However, there was no significant change in the levels of these parameters in the KTG. Conclusions. These results indicate that oxidative stress and inflammation developed in the liver tissue of the group that used ketamine and thiopental alone, suggesting that the KT form may be safer in terms of toxicity in the clinical usage. © 2022 by Wroclaw Medical University.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12928Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17219/acem/143573Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBedir, Zehra
dc.contributor.authorOzkaloglu Erdem, Kezban Tuna
dc.contributor.authorAtes, Irem
dc.contributor.authorOlmezturk Karakurt, Tulay Ceren
dc.contributor.authorGursul, Cebrail
dc.contributor.authorOnk, Didem
dc.contributor.authorKurt, Nezahat
dc.contributor.authorSuleyman, Zeynep
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:27:46.896918622Z
dc.date.available2026-10-18T20:27:46.896918622Z
dc.date.issued2022
dc.description.abstractBackground. In the literature, it has been suggested that ketamine-related oxidative organ damage results from increased blood adrenaline level, and thiopental-related oxidative damage is caused by decreased adrenaline level, suggesting that ketamine-thiopental combination (KT) may be beneficial in reducing the hepatotoxic effect of ketamine. Objectives. To biochemically investigate the effects of ketamine, thiopental and KT on the liver in rats. Materials and methods. Male albino Wistar type rats received intraperitoneally (ip.) 30 mg/kg ketamine in the ketamine alone (KG) group (n = 6), 15 mg/kg thiopental in the thiopental alone (TG) group (n = 6), and 30 mg/kg ketamine + 15 mg/kg thiopental in the ketamine+thiopental (KTG) group (n = 6). The same volume of distilled water as solvent was given to the healthy (HG) animal group. This procedure was repeated once daily for 30 days. At the end of this period, the animals were killed by decapitation and their livers were removed. In liver tissue, malondialdehyde (MDA), total glutathione (tGSH), total oxidant status (TOS), total antioxidant status (TAS), tumor necrosis factor alpha (TNF-α), interleukin 1 beta (IL-1β), and interleukin-6 (IL-6) levels were measured. The IL-1β, IL-6, TNF-α, adrenalin (ADR), noradrenalin (NDR), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) levels were determined in blood samples taken from the tail veins. Results. In the group treated with ketamine and thiopental alone, MDA, TOS, IL-1β, IL-6, TNF-α, ADR, NDR, ALT, and AST levels were found to be high, and those of tGSH and TAS to be low. However, there was no significant change in the levels of these parameters in the KTG. Conclusions. These results indicate that oxidative stress and inflammation developed in the liver tissue of the group that used ketamine and thiopental alone, suggesting that the KT form may be safer in terms of toxicity in the clinical usage. © 2022 by Wroclaw Medical University.
dc.identifier.doi10.17219/acem/143573
dc.identifier.eissn2451-2680
dc.identifier.endpage292
dc.identifier.issn1899-5276
dc.identifier.issue3
dc.identifier.pmid34918884
dc.identifier.scopus2-s2.0-85128160251
dc.identifier.startpage285
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12928
dc.identifier.volume31
dc.identifier.wosWOS:000733401000001
dc.language.isoen
dc.publisherWroclaw University of Medicine
dc.relation.ispartofAdvances in Clinical and Experimental Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHepatotoxicity
dc.subjectKetamine
dc.subjectRat
dc.subjectThiopental
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectLiver
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectTumor Necrosis Factor-alpha
dc.subjectalanine aminotransferase
dc.subjectaspartate aminotransferase
dc.subjectepinephrine
dc.subjectglutathione
dc.subjectinterleukin 1beta
dc.subjectinterleukin 6
dc.subjectmalonaldehyde
dc.subjectnoradrenalin
dc.subjecttumor necrosis factor
dc.subjectantioxidant
dc.subjectalanine aminotransferase blood level
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectaspartate aminotransferase blood level
dc.subjectaspartate aminotransferase level
dc.subjectbiochemical analysis
dc.titleEffects of ketamine, thiopental and their combination on the rat liver: A biochemical evaluation
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus10
rdl.citation.wos8
rdl.departmentDepartment of Anesthesiology and Reanimation, Mengucek Gazi Training and Research Hospital, Erzincan Binali Yildirim University, Turkey. | Department of Physiology, Faculty of Medicine, Erzincan Binali Yildirim University, Turkey. | Department of Anesthesiology and Reanimation, Faculty of Medicine, Erzincan Binali Yildirim University, Turkey. | Department of Biochemistry, Faculty of Medicine, Erzincan Binali Yildirim University, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yildirim University, Turkey. | Department of Nursing, Faculty of Health Sciences, Erzincan Binali Yildirim University, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)