The Molecular Mechanism of the Effect of Carvacrol on Desflurane Inhalation-Induced Liver Damage in Rats

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The metabolite of desflurane has been linked to hepatotoxicity. Carvacrol possesses antioxidant, antibacterial, antifungal, anticancer, anti-inflammatory, and spasmolytic properties, according to research. Our goal is to demonstrate that carvacrol protects rats’ livers against repeated doses of desflurane. Healthy (HG), desflurane (DS), and carvacrol + desflurane treatment (CDS) groups were formed from 18 albino male Wistar rats. A single dosage of carvacrol and 6% desflurane was given for 2 h on the 0th and 8th days. In the CDS group, the ALT and AST, MDA, TOS, NF-xB, TNF-α IL1 β levels were lower compared to the DS group (p < 0.001). The tGSH,TAS levels were found to be higher in the CDS group compared to the DS group (p < 0.001). It was determined that the mean degeneration level, Kupffer cell activation and PMNL infiltration were found to be lower compared to the DS group (p < 0.05).We confirmed that carvacol can be used in the treatment of desflurane-related liver injury. © 2022, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.

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AlanDeğerDil
dc.contributor.authorDisli, Zeliha Korkmaz
dc.contributor.authorAcun Delen, Leman
dc.contributor.authorTas, Hakan Gokalp
dc.contributor.authorKuyrukluyildiz, Ufuk
dc.contributor.authorDisli, Olcay Murat
dc.contributor.authorYazici, Gulce Naz
dc.contributor.authorCoban, Abdulkadir
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:27:43.914121676Z
dc.date.available2026-10-18T20:27:43.914121676Z
dc.date.issued2022
dc.description.abstractThe metabolite of desflurane has been linked to hepatotoxicity. Carvacrol possesses antioxidant, antibacterial, antifungal, anticancer, anti-inflammatory, and spasmolytic properties, according to research. Our goal is to demonstrate that carvacrol protects rats’ livers against repeated doses of desflurane. Healthy (HG), desflurane (DS), and carvacrol + desflurane treatment (CDS) groups were formed from 18 albino male Wistar rats. A single dosage of carvacrol and 6% desflurane was given for 2 h on the 0th and 8th days. In the CDS group, the ALT and AST, MDA, TOS, NF-xB, TNF-α IL1 β levels were lower compared to the DS group (p < 0.001). The tGSH,TAS levels were found to be higher in the CDS group compared to the DS group (p < 0.001). It was determined that the mean degeneration level, Kupffer cell activation and PMNL infiltration were found to be lower compared to the DS group (p < 0.05).We confirmed that carvacol can be used in the treatment of desflurane-related liver injury. © 2022, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.
dc.identifier.endpage137
dc.identifier.issn0326-2383
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85127149965
dc.identifier.startpage130
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12873
dc.identifier.volume41
dc.language.isoen
dc.publisherColegio de Farmaceuticos de la Provincia de Buenos Aires
dc.relation.ispartofLatin American Journal of Pharmacy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant
dc.subjectcarvacrol
dc.subjectdesflurane
dc.subjecthepatotoxicity
dc.subjectınhalation anesthesia
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectinterleukin 1beta
dc.subjectspasmolytic agent
dc.subjecttumor necrosis factor
dc.subjectalanine aminotransferase blood level
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantibacterial activity
dc.subjectantifungal activity
dc.subjectantiinflammatory activity
dc.subjectantineoplastic activity
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectaspartate aminotransferase blood level
dc.subjectcontrolled study
dc.subjectdrug induced cancer
dc.subjectenzyme linked immunosorbent assay
dc.subjecthistopathology
dc.subjectKupffer cell
dc.subjectliver
dc.subjectliver injury
dc.subjectliver toxicity
dc.subjectmale
dc.subjectmetabolite
dc.titleThe Molecular Mechanism of the Effect of Carvacrol on Desflurane Inhalation-Induced Liver Damage in Rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.source.indexSCOPUS