海马体
开阔地
成年男性
谷胱甘肽过氧化物酶
生理学
医学
抗氧化剂
肝酶
内科学
组织病理学
粪便
谷胱甘肽
内分泌学
氧化应激
动物科学
化学
生物
病理
酶
生物化学
过氧化氢酶
古生物学
作者
Orhan Baş,Hasan İlhan,Hatice Hancı,Hüseyin Çelikkan,Deniz Ekinci,Muhammet Değermenci,Burak Oğuzhan Karapınar,Aymen A. Warille,Soner Çankaya,Sezgin Özkasapoğlu
标识
DOI:10.1016/j.jchemneu.2023.102314
摘要
As the use of plastic-containing materials in our daily lives becomes increasingly common, exposure to nanoplastics accordingly becomes inevitable. Micro and nanoplastics released from large amounts of plastic waste constitute a serious environmental problem. Therefore, this study aimed to examine the effects of polystyrene nanoplastic (PS-NP) on the hippocampus. Thirty Wistar albino rats, 15 male and 15 female, aged 6–8 weeks, were used in the research. These were randomly divided into three groups of five males and five females each. A five-minute open field test was applied to all rats on the first and last days of the study. Three groups of rats (Control, NP1 and NP2) received the standard chow and water. Additionally, rats in the first neoplastic group (NP1) received 25 mg/kg PS-NP and rats in the second nanoplastic group (NP2) received 50 mg/kg PS-NP, at the same time each day by oral gavage. The rats were sacrificed under deep anesthesia at the end of four weeks. The hippocampi were removed and subjected to histopathological and biochemical analyses. Green fluorescent dots were detected in the hippocampi of both dose groups receiving nanoplastics (NPs) administered orally to female and male rats. Histopathological examination revealed neuronal degeneration in the hippocampi of male and female rats from both dose groups. However, while no significant difference was observed among the groups in terms of changes in antioxidant enzyme values and open-field test data in male rats, significant differences in peroxidase (POD) and glutathione S-transferase (GST) values and fecal boli and grooming numbers were determined in female rats exposed to NPs. In conclusion, exposure to NP substances extend as far as the hippocampus, causing neuronal damage and behavioral problems.
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