Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47597
Title: Chloroquine attenuates chronic hypoxia-induced testicular damage via suppressing endoplasmic reticulum stress and apoptosis in experimental rat model
Authors: Akin A.T.
Kaymak E.
Ceylan T.
Ozturk E.
Basaran K.E.
Karabulut D.
Ozdamar S.
Yakan, Birkan
Keywords: apoptosis
chloroquine
heat-shock proteins
hypoxia
male infertility
chloroquine
growth arrest and DNA damage inducible protein 153
heat shock protein 70
heat shock protein 90
hypoxia inducible factor 1alpha
adult
animal experiment
animal model
apoptosis
Article
blood sampling
controlled study
endoplasmic reticulum stress
enzyme linked immunosorbent assay
evaluation study
experimental rat
histopathology
hypoxia
immunohistochemistry
male
male fertility
nonhuman
protein expression
rat
testis injury
testis tissue
testosterone blood level
therapy effect
TUNEL assay
Wistar rat
Publisher: John Wiley and Sons Inc
Abstract: Chronic 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.
URI: https://doi.org/10.1111/1440-1681.13669
https://hdl.handle.net/11499/47597
ISSN: 0305-1870
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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