Evidence map›Paper›PMID 40380316›Full record

ArticleBMC anesthesiology2025

The effect of cerium oxide on liver in sevoflurane-administered rats: an experimental study.

Fazilet Erbay, Levent Öztürk, Merve Meryem Kıran, Gamze Gök, Mustafa Arslan

Abstract read
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Article in BMC anesthesiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Fazilet ErbayFazilet Erbay, Anesthesiology and Reanimation Clinic, Ankara Bilkent City Hospital, Ankara, Turkey. fazilettd@gmail.com.ORCID http://orcid.org/0000-0002-8764-5084
Levent ÖztürkDepartment of Anesthesiology and Reanimation, Ankara Yıldırım Beyazıt University, Ankara, Turkey.ORCID http://orcid.org/0000-0001-9755-033X
Merve Meryem KıranDepartment of Pathology, Ankara Bilkent City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-2498-0472
Gamze GökDepartment of Biochemistry, Ankara Bilkent City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-2804-5548
Mustafa ArslanDepartment of Anesthesiology and Reanimation, Gazi University, Ankara, Turkey.ORCID http://orcid.org/0000-0003-4882-5063

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevoflurane, a commonly used inhalational anesthetic, has been associated with hepatotoxicity, although reports are often isolated. Cerium oxide nanoparticles (CeO₂) are effective free radical scavengers with potential therapeutic applications for oxidative stress-related damage. This study aimed to evaluate the protective effects of CeO₂ on liver damage in sevoflurane-administered rats.

methodsA total of 24 male Wistar albino rats were randomized into four groups: Control (C), Sevoflurane (S), Cerium Oxide (CeO₂), and Sevoflurane + Cerium Oxide (S + CeO₂). Sevoflurane was administered at 2% concentration with 100% oxygen at 4 L/min for 2 h in Groups S and S + CeO₂. CeO₂ (0.5 mg/kg) was administered intravenously in Groups CeO₂ and S + CeO₂. Biochemical analyses of alanine transaminase (ALT), aspartate transaminase (AST), lactate dehydrogenase (LDH), hemoglobin (Hgb), and hematocrit (Hct) were performed, and liver tissues were examined histopathologically.

resultsHydropic degeneration and neutrophil infiltration were significantly lower in Group CeO₂ compared to Group S. Group S showed elevated AST and LDH levels compared to the control (p < 0.05). Although AST levels were lower in Groups CeO₂ and S + CeO₂ than in Group S, the difference was not statistically significant. LDH levels were significantly lower in Group S + CeO₂ compared to Group S (p = 0.045). Histopathological examination confirmed reduced liver damage in CeO₂-treated groups.

conclusionsThis study is of significance since it is the first experimental study on the effect of CeO2 on liver damage caused by sevoflurane. Cerium oxide demonstrated potential in mitigating sevoflurane-induced liver damage. Further research is warranted to explore the clinical relevance of CeO₂ in hepatic injury.

Indexed as

Anesthetics, InhalationCeriumChemical and Drug Induced Liver InjuryLiverMethyl EthersAlanine TransaminaseAnimalsAspartate AminotransferasesMaleRandom AllocationRatsRats, WistarSevofluraneAlanine TransaminaseAnesthetics, InhalationAspartate Aminotransferasesceric oxideCeriumMethyl EthersSevofluraneCerium oxideLiver damageNanoparticlesOxidative stressSevoflurane

Identifiers

PMID40380316
PMCPMC12083047

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.