<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-19T01:47:49Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/12106" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/12106</identifier><datestamp>2026-10-18T20:27:03Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>The Effect of Carvacrol on Oxidative and Inflammatory Liver Damage due to Staphylococcus aureus Infection in Rats</dc:title><dc:creator>Dabanlioglu, Bulent</dc:creator><dc:creator>Suleyman, Bahadir</dc:creator><dc:creator>Mammadov, Renad</dc:creator><dc:creator>Coban, Taha Abdulkadir</dc:creator><dc:creator>Yazici, Gulce Naz</dc:creator><dc:creator>Akyuz, Sumeyye</dc:creator><dc:creator>Yavuzer, Bulent</dc:creator><dc:creator>Bulut, Seval</dc:creator><dc:creator>Suleyman, Halis</dc:creator><dc:subject>carvacrol</dc:subject><dc:subject>cefazolin</dc:subject><dc:subject>liver damage</dc:subject><dc:subject>rat</dc:subject><dc:subject>Staphylococcus aureus</dc:subject><dc:subject>alanine aminotransferase</dc:subject><dc:subject>aspartate aminotransferase</dc:subject><dc:subject>glutathione</dc:subject><dc:subject>immunoglobulin enhancer binding protein</dc:subject><dc:subject>interleukin 1beta</dc:subject><dc:subject>malonaldehyde</dc:subject><dc:subject>thiopental</dc:subject><dc:subject>tumor necrosis factor</dc:subject><dc:subject>animal experiment</dc:subject><dc:subject>animal model</dc:subject><dc:subject>animal tissue</dc:subject><dc:subject>antibacterial activity</dc:subject><dc:subject>antibiotic sensitivity</dc:subject><dc:subject>antiinflammatory activity</dc:subject><dc:subject>antimicrobial activity</dc:subject><dc:subject>antioxidant activity</dc:subject><dc:subject>Article</dc:subject><dc:subject>biochemical analysis</dc:subject><dc:subject>colony forming unit</dc:subject><dc:subject>controlled study</dc:subject><dc:subject>disk diffusion</dc:subject><dc:subject>drug efficacy</dc:subject><dc:subject>drug megadose</dc:subject><dc:subject>enzyme linked immunosorbent assay</dc:subject><dc:subject>histopathology</dc:subject><dc:description>SUMMARY. Staphylococcus aureus is a bacterial pathogen that can cause oxidative stress. Carvacrol has anti-microbial, antioxidant, anti-inflammatory and hepatoprotective effects. This study evaluated the antibacterial effect of carvacrol and its effect on liver damage by S. aureus. The rats were divided into four groups: con-trol(HG), S. aureus injected (SaG), S. aureus + carvacrol (SaC), and S. aureus + cefazolin (SaCF). S. aureus was injected intraperitoneally (ip) to the SaG, SaC and SaCF groups. 24 h after the injection, carvacrol was given to the SaC group and cefazolin to the SaCF group as ip. Carvacrol and cefazolin administration was continued for 7 days. According to our antibiogram results, although the antibacterial effect of carvacrol was weaker than cefazolin, it prevented the increase of malondialdehyde (MDA), aminotransferase (ALT), aspar-tate aminotransferase (AST) and proinflammatory cytokines and the decrease of total glutathione (tGSH) better (p &lt; 0.001). It also managed histopathological damage better than cefazolin. The results indicate that carvacrol may be helpful in the treatment of liver damage from infection. © 2023, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.</dc:description><dc:publisher>Colegio de Farmaceuticos de la Provincia de Buenos Aires</dc:publisher><dc:date>2023</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/12106</dc:identifier><dc:identifier>0326-2383</dc:identifier><dc:language>en</dc:language><dc:relation>Latin American Journal of Pharmacy</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/12106</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>