<?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>2026-10-19T01:05:37Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/11932" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/11932</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>Protective Effect of Adenosine Triphosphate against 5-Fluorouracil-Induced Oxidative Ovarian Damage in vivo</dc:title><dc:creator>Ozer, Mehmet</dc:creator><dc:creator>Ince, Sefa</dc:creator><dc:creator>Altuner, Durdu</dc:creator><dc:creator>Suleyman, Zeynep</dc:creator><dc:creator>Cicek, Betul</dc:creator><dc:creator>Gulaboglu, Mine</dc:creator><dc:creator>Mokhtare, Behzad</dc:creator><dc:creator>Gursul, Cebrail</dc:creator><dc:creator>Suleyman, Halis</dc:creator><dc:subject>5</dc:subject><dc:subject>adenosine triphosphate</dc:subject><dc:subject>fluorouracil</dc:subject><dc:subject>inflammation</dc:subject><dc:subject>ovarian</dc:subject><dc:subject>rat</dc:subject><dc:subject>reproductive</dc:subject><dc:subject>Animals</dc:subject><dc:subject>Female</dc:subject><dc:subject>Ovary</dc:subject><dc:subject>Oxidative Stress</dc:subject><dc:subject>Rats</dc:subject><dc:subject>animal</dc:subject><dc:description>Objective: The aim of our study was to analyze the effect of ATP on possible ovarian damage of 5-FU in rats. Methods: The animals were divided to three groups; healthy group (HG), 5-FU alone group (FUG) and ATP+5-FU administered group (AFU). The ATP 4 mg/kg was injected intraperitoneally (IP) into the AFU group. The same volume of saline (0.9% NaCl) as the solvent was administered intraperitoneally to the HG and FUG groups. One hour after administering ATP and solvent, 5-FU 100 mg/kg was injected intraperitoneally to the animals in the AFU and FUG groups. ATP was administered to the animals once a day for 10 days. On the 1st, 3rd and 5th days of 5-FU, one dose (total of 3 doses) was administered. On day 10, the animals were euthanasia with high-dose anaesthesia and ovarian tissues were removed. The removed ovaries were analyzed biochemically andhistopathological. Result: ATP significantly suppressed both the increase in MDA and IL-6 levels, and the decrease in tGSH, SOD and CAT levels. Treatment with ATP significantly suppressed the severe vacuolization and primordial follicle degeneration induced by 5-FU in our study. Conclusion: ATP was possible to be useful for the treatment of 5-FU-induced ovarian damage. © This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License.</dc:description><dc:publisher>Asian Pacific Organization for Cancer Prevention</dc:publisher><dc:date>2023</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/11932</dc:identifier><dc:identifier>https://doi.org/10.31557/apjcp.2023.24.3.1007</dc:identifier><dc:identifier>1513-7368</dc:identifier><dc:language>en</dc:language><dc:relation>Asian Pacific Journal of Cancer Prevention</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/11932</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>