<?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>2026-10-19T01:36:02Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/12310" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/12310</identifier><datestamp>2026-10-18T21:13:21Z</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>Molecular mechanism of the protective effect of adenosine triphosphate against paracetamol-induced liver toxicity in rats</dc:title><dc:creator>Koç, Alparslan</dc:creator><dc:creator>Gazi, Mustafa</dc:creator><dc:creator>Caner Sayar, Ali</dc:creator><dc:creator>Onk, Didem</dc:creator><dc:creator>Ali Arı, Muhammet</dc:creator><dc:creator>Süleyman, Bahadır</dc:creator><dc:creator>Gökhan Ağgül, Ahmet</dc:creator><dc:creator>Altındağ, Fikret</dc:creator><dc:creator>Altuner, Durdu</dc:creator><dc:creator>Süleyman, Halis</dc:creator><dc:subject>ATP</dc:subject><dc:subject>Liver toxicity</dc:subject><dc:subject>Pain</dc:subject><dc:subject>Paracetamol</dc:subject><dc:subject>Acetaminophen</dc:subject><dc:subject>Adenosine Triphosphate</dc:subject><dc:subject>Animals</dc:subject><dc:subject>Antioxidants</dc:subject><dc:subject>Chemical and Drug Induced Liver Injury</dc:subject><dc:subject>Liver</dc:subject><dc:subject>Oxidative Stress</dc:subject><dc:subject>Rats</dc:subject><dc:subject>catalase</dc:subject><dc:subject>glutathione</dc:subject><dc:subject>malonaldehyde</dc:subject><dc:subject>superoxide dismutase</dc:subject><dc:subject>antioxidant</dc:subject><dc:subject>alanine aminotransferase blood level</dc:subject><dc:subject>animal experiment</dc:subject><dc:subject>animal model</dc:subject><dc:subject>animal tissue</dc:subject><dc:subject>Article</dc:subject><dc:subject>aspartate aminotransferase level</dc:subject><dc:subject>controlled study</dc:subject><dc:subject>drug mechanism</dc:subject><dc:subject>edema</dc:subject><dc:subject>enzyme activity</dc:subject><dc:subject>fibrosis</dc:subject><dc:subject>histopathology</dc:subject><dc:subject>lipid storage</dc:subject><dc:description>Toxic doses of paracetamol are also known to be close to therapeutic doses. This study aimed to biochemically investigate the protective effect of ATP against paracetamol-induced oxida-tive liver injury in rats and to examine the tissues histopathologically. We divided the animals into the paracetamol alone (PCT), ATP + paracetamol (PATP), and healthy control (HG) groups. Liver tissues were examined biochemically and histopathologically. Malondialdehyde level, AST and ALT activity in the PCT group were significantly higher than those in the HG and PATP groups (p &lt; 0.001). The glutathione (tGSH) level, superoxide dismutase (SOD) and catalase (CAT) activity in the PCT group was significantly lower than that in the HG and PATP groups (p &lt; 0.001), while animal SOD activity was significantly different between the PATP and HG groups (p &lt; 0.001). The activity of CAT was almost the same. In the group treated with paracetamol alone, lipid deposition, necrosis, fibrosis, and grade 3 hydropic degeneration were observed. No histopathological damage was observed of the ATP-treated group, except for grade 2 edema. We discovered that ATP reduces the oxidative stress caused by paracetamol ingestion and protects against paracetamol-induced liver injury at the macroscopic and histological levels. © The Authors 2023.</dc:description><dc:publisher>Slovak Academy of Sciences</dc:publisher><dc:date>2023</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/12310</dc:identifier><dc:identifier>https://doi.org/10.4149/gpb_2022055</dc:identifier><dc:identifier>0231-5882</dc:identifier><dc:language>en</dc:language><dc:relation>General Physiology and Biophysics</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/12310</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>