<?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>2026-10-19T01:02:03Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10760" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10760</identifier><datestamp>2026-10-18T21:13:05Z</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>Effects of adenosine triphosphate and reduced glutathione on biochemical, histopathological and immunofluorescence alterations associated with atezolizumab-induced cardiac tissue injury</dc:title><dc:creator>Yasar, Yesim Kaya</dc:creator><dc:creator>Sezgin, Esra Tuba</dc:creator><dc:creator>Suleyman, Bahadir</dc:creator><dc:creator>Mammadov, Renad</dc:creator><dc:creator>Ozkaraca, Mustafa</dc:creator><dc:creator>Gungor, Ali</dc:creator><dc:creator>Coban, Taha Abdulkadir</dc:creator><dc:creator>Suleyman, Halis</dc:creator><dc:subject>adenosine triphosphate</dc:subject><dc:subject>atezolizumab</dc:subject><dc:subject>cardiac injury</dc:subject><dc:subject>glutathione</dc:subject><dc:subject>inflammation</dc:subject><dc:subject>myocarditis</dc:subject><dc:subject>oxidative stress</dc:subject><dc:subject>rat</dc:subject><dc:description>Background – In this study, the potential protective effects of adenosine triphosphate (ATP) and glutathione (GSH) against atezolizumab-induced cardiac injury in rat heart tissue were investigated. Methods – A total of 24 male albino Wistar rats were used in the experiment. The animals were divided into four groups: healthy group adenosine triphosphate + atezolizumab (ATAZ), GSH + atezolizumab (GHAZ), and atezolizumab alone (ATZ). ATP was administered intraperitoneally at a dose of 4 mg/kg, while GSH was administered orally at a dose of 200 mg/kg for 7 days. Atezolizumab was administered intraperitoneally to the experimental groups at a dose of 10 mg/kg twice weekly. At the end of the experiment, malondialdehyde total glutathione (tGSH), superoxide dismutase catalase, interleukin-1β (IL-1β), and interleukin-6 (IL-6) levels in heart tissues were measured using biochemical methods. In addition, histopathological and immunofluorescence examinations were performed. Results – The results showed that oxidative stress and inflammation markers increased, whereas antioxidant parameters decreased in the atezolizumab-treated group. ATP and GSH administration significantly attenuated these changes and exerted protective effects on cardiac tissue. Conclusion – Overall, ATP and GSH ameliorated the biochemical, histopathological, and immunofluorescence changes associated with atezolizumab-induced cardiac injury in this experimental model. Copyright © 2026 Yasar, Sezgin, Suleyman, Mammadov, Ozkaraca, Gungor, Coban and Suleyman.</dc:description><dc:publisher>Frontiers Media SA</dc:publisher><dc:date>2026</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/10760</dc:identifier><dc:identifier>https://doi.org/10.3389/fphar.2026.1914819</dc:identifier><dc:identifier>1663-9812</dc:identifier><dc:language>en</dc:language><dc:relation>Frontiers in Pharmacology</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/10760</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>