<?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>2026-10-19T01:18:23Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/14503" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/14503</identifier><datestamp>2026-10-18T21:14:21Z</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>Effects of Pycnogenol on cisplatin-induced optic nerve injury: an experimental study</dc:title><dc:creator>Icel, Erel</dc:creator><dc:creator>Uçak, Turgay</dc:creator><dc:creator>Agcayazi, Burcu</dc:creator><dc:creator>Karakurt, Yücel</dc:creator><dc:creator>Yilmaz, Hayati</dc:creator><dc:creator>Keskin Çimen, Ferda</dc:creator><dc:creator>Süleyman, Halis</dc:creator><dc:subject>cisplatin</dc:subject><dc:subject>malondialdehyde</dc:subject><dc:subject>optic nerve damage</dc:subject><dc:subject>oxidative stress</dc:subject><dc:subject>Pycnogenol</dc:subject><dc:subject>Animals</dc:subject><dc:subject>Antineoplastic Agents</dc:subject><dc:subject>Antioxidants</dc:subject><dc:subject>Flavonoids</dc:subject><dc:subject>Inflammation</dc:subject><dc:subject>Lipid Peroxidation</dc:subject><dc:subject>Male</dc:subject><dc:subject>Optic Nerve</dc:subject><dc:subject>Optic Nerve Injuries</dc:subject><dc:subject>Plant Extracts</dc:subject><dc:subject>Rats</dc:subject><dc:subject>Rats, Wistar</dc:subject><dc:subject>Tumor Necrosis Factor-alpha</dc:subject><dc:subject>glutathione</dc:subject><dc:subject>immunoglobulin enhancer binding protein</dc:subject><dc:subject>malonaldehyde</dc:subject><dc:subject>tumor necrosis factor</dc:subject><dc:subject>antineoplastic agent</dc:subject><dc:subject>antioxidant</dc:subject><dc:subject>flavonoid</dc:subject><dc:subject>plant extract</dc:subject><dc:subject>pycnogenols</dc:subject><dc:subject>animal experiment</dc:subject><dc:subject>animal model</dc:subject><dc:subject>animal tissue</dc:subject><dc:description>Aim: To determine the effects of Pycnogenol on cisplatin-induced optic nerve damage. Material and method: Totally 18 albino Wistar male rats were assigned into three groups, with six rats in each group as follows: healthy controls (HC group), only cisplatin (2.5 mg/kg) administered group (CIS group) and Pycnogenol (40 mg/kg) + cisplatin (2.5 mg/kg) administered group (PYC group). We analyzed the levels of malondialdehyde (MDA) as a marker of lipid peroxidation and oxidative stress, total glutathione (tGSH) as a marker of antioxidant status, nuclear factor-kappa B (NF-κB) and tumor necrosis factor alpha (TNF-α) as inflammatory markers, total oxidative status (TOS) and total antioxidant status (TAS) on eye tissue together with histopathological evaluation of optic nerve in an experimental model. Results: In CIS group MDA, TOS, TNF-α and NF-κB levels were statistically significantly higher (p &lt; 0.001) than HC group while tGSH and TAS levels were significantly lower (p &lt; 0.001). On the other hand, in PYC group MDA, TOS, TNF-α and NF-κB levels were statistically significantly lower (p &lt; 0.001) than CIS group while tGSH and TAS levels were significantly higher (p &lt; 0.001). Conclusion: Pycnogenol pretreatment was highly effective in preventing augmentation of cisplatin-induced oxidative stress and inflammation in eye tissue. © 2018, © 2018 Informa UK Limited, trading as Taylor &amp; Francis Group.</dc:description><dc:publisher>Taylor and Francis Ltd</dc:publisher><dc:date>2018</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/14503</dc:identifier><dc:identifier>https://doi.org/10.1080/15569527.2018.1495224</dc:identifier><dc:identifier>1556-9527</dc:identifier><dc:language>en</dc:language><dc:relation>Cutaneous and Ocular Toxicology</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/14503</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>