<?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>2026-10-18T23:53:46Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/14982" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/14982</identifier><datestamp>2026-10-18T21:14:26Z</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 melatonin on oxidative stress and apoptosis in experimental diabetes mellitus-related ovarian injury</dc:title><dc:creator>Nayki, Umit</dc:creator><dc:creator>Onk, Didem</dc:creator><dc:creator>Balci, Gurhan</dc:creator><dc:creator>Nayki, Cenk</dc:creator><dc:creator>Onk, Alper</dc:creator><dc:creator>Çankaya, Murat</dc:creator><dc:creator>Taskin Kafa, Ayse Humeyra</dc:creator><dc:creator>Kuzucu, Mehmet</dc:creator><dc:subject>Apoptosis</dc:subject><dc:subject>diabetes</dc:subject><dc:subject>NFkB pathway</dc:subject><dc:subject>ovary</dc:subject><dc:subject>oxidative stress</dc:subject><dc:subject>rat</dc:subject><dc:subject>Animals</dc:subject><dc:subject>Caspase 3</dc:subject><dc:subject>Diabetes Mellitus, Experimental</dc:subject><dc:subject>Female</dc:subject><dc:subject>Melatonin</dc:subject><dc:subject>NF-kappa B</dc:subject><dc:subject>Rats</dc:subject><dc:subject>Rats, Sprague-Dawley</dc:subject><dc:subject>catalase</dc:subject><dc:subject>immunoglobulin enhancer binding protein</dc:subject><dc:subject>malonaldehyde</dc:subject><dc:subject>superoxide dismutase</dc:subject><dc:subject>animal experiment</dc:subject><dc:subject>animal model</dc:subject><dc:subject>animal tissue</dc:subject><dc:subject>antioxidant activity</dc:subject><dc:subject>Article</dc:subject><dc:subject>controlled study</dc:subject><dc:subject>diabetes mellitus</dc:subject><dc:subject>drug effect</dc:subject><dc:subject>enzyme activity</dc:subject><dc:subject>experimental diabetes mellitus</dc:subject><dc:subject>histopathology</dc:subject><dc:subject>immunohistochemistry</dc:subject><dc:description>We aimed to evaluate the effect of melatonin on oxidative stress and ovarian injury in rats. Twenty-four Sprague-Dawley albino rats were divided into three groups: Group 1 as nondiabetic healthy controls (n = 8), group 2 as nontreated diabetic rats (n = 8) and group 3 as melatonin-treated diabetic rats (n = 8). After overt diabetes was produced by intraperitoneal injection of streptozosin, 20 mg/kg/day of melatonin was given intraperitoneally to group 3 for a week. NF-kB and caspase-3 immunoexpressions, lipid peroxidation, the activities of antioxidative enzymes, total oxidant capacity and total antioxidant capacity were assessed. Immunoexpressions of NF-kB and caspase-3 were significantly lower in group 3 than group 2. There was a significant decrease in superoxide dismutase activity in group 2 than group 1 and a significant increase in group 3 compared with group 2. We observed a nonsignificant decrease in catalase activity between group 1 and group 2 and a nonsignificant increase between group 2 and group 3. There was a nonsignificant increase in the plasma level of total oxidant status in group 2 than group 1, but a significant decrease was observed in group 3 compared to group 2. Total antioxidant status was significantly lower in group 2 compared with group 1 and group 3. In conclusion, melatonin ameliorates the negative effects of oxidative stress on DM-related ovarian injury. © 2015 Taylor &amp; Francis.</dc:description><dc:publisher>Taylor and Francis Ltd</dc:publisher><dc:date>2016</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/14982</dc:identifier><dc:identifier>https://doi.org/10.3109/09513590.2015.1126819</dc:identifier><dc:identifier>0951-3590</dc:identifier><dc:language>en</dc:language><dc:relation>Gynecological Endocrinology</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/14982</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>