Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47597
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dc.contributor.authorAkin A.T.-
dc.contributor.authorKaymak E.-
dc.contributor.authorCeylan T.-
dc.contributor.authorOzturk E.-
dc.contributor.authorBasaran K.E.-
dc.contributor.authorKarabulut D.-
dc.contributor.authorOzdamar S.-
dc.contributor.authorYakan, Birkan-
dc.date.accessioned2023-01-09T21:29:20Z-
dc.date.available2023-01-09T21:29:20Z-
dc.date.issued2022-
dc.identifier.issn0305-1870-
dc.identifier.urihttps://doi.org/10.1111/1440-1681.13669-
dc.identifier.urihttps://hdl.handle.net/11499/47597-
dc.description.abstractChronic hypoxia negatively affects male fertility by causing pathological changes in male reproductive system. However, underlying mechanisms of this damage are unknown. Chloroquine (CLQ) is an anti-inflammatory agent that is widely used in the treatment of inflammation-related diseases such as malaria and rheumatoid arthritis. This study aimed to investigate the therapeutic effects of CLQ in the hypoxia-induced testicular damage via assessment of hypoxic response, endoplasmic reticulum stress and apoptosis. For this purpose, 32 Wistar albino rats were divided into 4 groups as control (given 20%-21% O2, no treatment), CLQ (given 50 mg/kg and 20%-21% O2 for 28 days), hypoxia (HX) (given 10% O2 for 28 days) and HX + CLQ (given 50 mg/kg and 10% O2 for 28 days). After the experiment, blood samples and testicular tissues were taken. Histopathological evaluation was performed on testicular tissues and hypoxia-inducible factor 1-? (HIF1-?), heat shock proteins (HSPs) HSP70, HSP90 and growth arrest and DNA damage-inducible gene 153 (GADD153) expression levels were detected via immunohistochemistry. Moreover, apoptotic cells were detected via terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL) staining and serum testosterone levels were determined by enzyme-linked immunosorbent assay (ELISA) assay. Histopathological changes, apoptotic cell numbers and HIF1-?, HSP70, HSP90 and GADD153 expressions significantly increased in HX group (P <.05). Moreover, serum testosterone levels decreased in this group (P >.05). However, CLQ exerted a strong ameliorative effect on all parameters in HX + CLQ group. According to our results, we suggested that CLQ can be considered as an alternative protective agent for eliminating the negative effects of hypoxic conditions on male fertility. © 2022 John Wiley & Sons Australia, Ltd.en_US
dc.description.sponsorshipThe authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: the cost of the experimental animals used in this experimental study has been covered by a grant from the research and technology department of Erciyes University.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.relation.ispartofClinical and Experimental Pharmacology and Physiologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectapoptosisen_US
dc.subjectchloroquineen_US
dc.subjectheat-shock proteinsen_US
dc.subjecthypoxiaen_US
dc.subjectmale infertilityen_US
dc.subjectchloroquineen_US
dc.subjectgrowth arrest and DNA damage inducible protein 153en_US
dc.subjectheat shock protein 70en_US
dc.subjectheat shock protein 90en_US
dc.subjecthypoxia inducible factor 1alphaen_US
dc.subjectadulten_US
dc.subjectanimal experimenten_US
dc.subjectanimal modelen_US
dc.subjectapoptosisen_US
dc.subjectArticleen_US
dc.subjectblood samplingen_US
dc.subjectcontrolled studyen_US
dc.subjectendoplasmic reticulum stressen_US
dc.subjectenzyme linked immunosorbent assayen_US
dc.subjectevaluation studyen_US
dc.subjectexperimental raten_US
dc.subjecthistopathologyen_US
dc.subjecthypoxiaen_US
dc.subjectimmunohistochemistryen_US
dc.subjectmaleen_US
dc.subjectmale fertilityen_US
dc.subjectnonhumanen_US
dc.subjectprotein expressionen_US
dc.subjectraten_US
dc.subjecttestis injuryen_US
dc.subjecttestis tissueen_US
dc.subjecttestosterone blood levelen_US
dc.subjecttherapy effecten_US
dc.subjectTUNEL assayen_US
dc.subjectWistar raten_US
dc.titleChloroquine attenuates chronic hypoxia-induced testicular damage via suppressing endoplasmic reticulum stress and apoptosis in experimental rat modelen_US
dc.typeArticleen_US
dc.identifier.volume49en_US
dc.identifier.issue8en_US
dc.identifier.startpage813en_US
dc.identifier.endpage823en_US
dc.identifier.doi10.1111/1440-1681.13669-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57196939064-
dc.authorscopusid57188632370-
dc.authorscopusid57221313801-
dc.authorscopusid36131874700-
dc.authorscopusid57050249800-
dc.authorscopusid56595045000-
dc.authorscopusid6701347161-
dc.identifier.pmid35579513en_US
dc.identifier.scopus2-s2.0-85131385159en_US
dc.identifier.wosWOS:000807828500001en_US
dc.identifier.scopusqualityQ2-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Sağlık Bilimleri Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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