Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47602
Title: Effects of fish oil on methotrexate-induced reproductive damage in rats
Authors: Ipek V.
Kaya K.
Cebi C.
Gurel A.
Ayozger L.E.O.
Keywords: apoptosis
fish oil
histopathology
methotrexate
oxidative stress
caspase 3
catalase
fish oil
glutathione
glutathione peroxidase
methotrexate
superoxide dismutase
thiobarbituric acid reactive substance
antioxidant
fish oil
glutathione
methotrexate
superoxide dismutase
thiobarbituric acid reactive substance
animal cell
animal experiment
animal model
animal tissue
Article
biochemical analysis
controlled study
enzyme activity
general anesthesia
germ cell
histology
histopathology
immunohistochemistry
male
nonhuman
rat
reproductive toxicity
semen parameters
sperm count
sperm quality
sperm viability
spermatozoon motility
animal
metabolism
oxidative stress
sperm
Animals
Antioxidants
Fish Oils
Glutathione
Male
Methotrexate
Oxidative Stress
Rats
Semen
Sperm Motility
Superoxide Dismutase
Thiobarbituric Acid Reactive Substances
Publisher: John Wiley and Sons Inc
Abstract: Methotrexate (MTX) is a folic acid antagonist that is commonly used in paediatric and adult oncology to treat a variety of malignancies. Internal organs, including the testis, are severely cytotoxic and genotoxic to MTX. Omega-3, as an antioxidant, has been shown to protect rat testis tissue from injury. The effect of fish oil (FO) on MTX-induced reproductive damage in rats was investigated in this work. The 28 animals were divided into four groups for this purpose (control, FO, MTX, and MTX-FO). On the third day, the MTX group received a single intraperitoneal injection of 20 mg/kg MTX. Furthermore, in the FO and MTX-FO groups, FO was delivered through gavage once daily for 14 days. All animals euthanized under general anaesthesia on the 15th day. TBARS, catalase, glutathione peroxidase, glutathione (GSH), superoxide dismutase levels were measured biochemically. The Cosentino grading system was utilized for histology. Germ cell thickness and caspase-3 activity were also evaluated. In addition, sperm motility rate, epididymal sperm count, aberrant sperm rate, and sperm vitality were measured to assess sperm quality. Some TBARS levels have increased, but GSH levels decreased significantly in the MTX group. FO reduced TBARS levels while considerably increasing GSH levels. All sperm quality measures were significantly lowered in the MTX group, while FO had a recovery effect. There were no notable variations in histopathology across groups except for germ cell thickness, which reduced considerably in the MTX group and recovered with FO treatment. As a result, FO has been shown to reduce testicular toxicity following MTX treatment in rats. © 2022 Wiley-VCH GmbH.
URI: https://doi.org/10.1111/and.14638
https://hdl.handle.net/11499/47602
ISSN: 0303-4569
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

Show full item record



CORE Recommender

SCOPUSTM   
Citations

1
checked on May 5, 2024

WEB OF SCIENCETM
Citations

1
checked on May 6, 2024

Page view(s)

36
checked on May 6, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.