Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/54839
Title: Investigation of protective effect of ellagic acid in phthalates-induced reproductive damage
Authors: Başak, Türkmen, N.
Ayhan, İ.
Taşlıdere, A.
Aydın, M.
Çiftçi, O.
Keywords: antioxidant
DBP
Ellagic acid
phthalate
reproductive damage
carboxymethylcellulose
catalase
ellagic acid
glutathione
glutathione peroxidase
malonaldehyde
phthalic acid
superoxide dismutase
thiobarbituric acid reactive substance
antioxidant
ellagic acid
malonaldehyde
phthalic acid
phthalic acid derivative
adult
animal cell
animal experiment
animal tissue
antioxidant activity
Article
cell cycle arrest
cell loss
cell structure
cell vacuole
concentration ratio
controlled study
data analysis software
desquamation
edema
germ cell
histopathology
hyperemia
male
nonhuman
oxidative stress
protein expression level
rat
reproductive toxicity
seminiferous tubule epithelium
sperm count
spermatocyte
spermatozoon abnormality
spermatozoon density
spermatozoon head
spermatozoon motility
spermatozoon tail
testis tissue
thickness
upregulation
animal
human
metabolism
reproduction
spermatozoon motility
Sprague Dawley rat
testis
Animals
Antioxidants
Ellagic Acid
Humans
Male
Malondialdehyde
Oxidative Stress
Phthalic Acids
Rats
Rats, Sprague-Dawley
Reproduction
Sperm Motility
Testis
Publisher: Taylor and Francis Ltd.
Abstract: Phthalates that people are exposed to every day are toxic carcinogenic chemicals with proven harmful effects on growth and reproduction. Ellagic acid (EA) is a polyphenol derivative known for its antioxidant properties. We hypothesized that the possible reproductive damage mechanism of phthalates is oxidative attack and ellagic acid could have a protective effect against radical forms in the body through its antioxidant properties. Thirty-two male rats were randomly divided into 4 groups, with 8 rats in each. Phthalate (DBP) was administered intraperitoneally and EA acid through gastric oral gavage (phthalate group 500 mg/kg/day DBP; EA group 2 mg/kg/day ellagic acid; the treatment group 500 mg/kg/day DBP and 2 mg/kg/day EA). The vehicle of DBP and EA, carboxymethyl cellulose was administered to control group. At the end of 4 weeks the testis tissue samples were taken under mild anesthesia. Tissue malondialdehyde, antioxidant parameters, sperm motility, sperm density and abnormal spermatozoon ratios were determined. Analysis was performed with One Way ANOVA test using SPSS 12.0 program. As a result; it has been shown that DBP causes oxidative damage by increasing the malondialdehyde level and decreasing antioxidant parameters, increased abnormal sperm rate and decreased sperm motility and concentration and histopathological damage so this damage is inhibited by the antioxidant activity of ellagic acid. © 2020 Informa UK Limited, trading as Taylor & Francis Group.
URI: https://doi.org/10.1080/01480545.2020.1853764
https://hdl.handle.net/11499/54839
ISSN: 0148-0545
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu

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