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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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