To what extent are orally ingested nanoplastics toxic to the hippocampus in young adult rats?

IF 2.7 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Orhan Baş , Hasan İlhan , Hatice Hancı , Hüseyin Çelikkan , Deniz Ekinci , Muhammet Değermenci , Burak Oğuzhan Karapınar , Aymen A. Warille , Soner Çankaya , Sezgin Özkasapoğlu
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Abstract

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.

Material and method

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.

Results

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.

口服纳米塑料对年轻成年大鼠海马体的毒性有多大?
随着含塑料材料在我们日常生活中的使用越来越普遍,接触纳米塑料也变得不可避免。从大量塑料垃圾中释放出的微塑料和纳米塑料构成了一个严重的环境问题。因此,本研究旨在检测聚苯乙烯纳米塑料(PS-NP)对海马的影响。材料和方法:选用30只Wistar白化大鼠,雄性15只,雌性15只,年龄6-8周。他们被随机分为三组,每组五名男性和五名女性。在研究的第一天和最后一天,对所有大鼠进行了5分钟的野外试验。三组大鼠(对照组、NP1和NP2)接受标准食物和水。此外,第一肿瘤组(NP1)中的大鼠每天同时口服25 mg/kg PS-NP,第二纳米塑料组(NP2)中的小鼠每天同时接受50 mg/kg PS-NP。在四周结束时,在深度麻醉下处死大鼠。移除海马并进行组织病理学和生化分析。结果:雌性和雄性大鼠口服纳米塑料后,在两个剂量组的海马中都检测到绿色荧光点。组织病理学检查显示,两个剂量组的雄性和雌性大鼠的海马出现神经元变性。然而,尽管雄性大鼠的抗氧化酶值和开放试验数据的变化在各组之间没有观察到显著差异,但暴露于NP的雌性大鼠的过氧化物酶(POD)和谷胱甘肽S-转移酶(GST)值以及粪便代谢和梳理数目的变化却存在显著差异。总之,暴露于NP物质会延伸到海马体,导致神经元损伤和行为问题。
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来源期刊
Journal of chemical neuroanatomy
Journal of chemical neuroanatomy 医学-神经科学
CiteScore
4.50
自引率
3.60%
发文量
87
审稿时长
62 days
期刊介绍: The Journal of Chemical Neuroanatomy publishes scientific reports relating the functional and biochemical aspects of the nervous system with its microanatomical organization. The scope of the journal concentrates on reports which combine microanatomical, biochemical, pharmacological and behavioural approaches. Papers should offer original data correlating the morphology of the nervous system (the brain and spinal cord in particular) with its biochemistry. The Journal of Chemical Neuroanatomy is particularly interested in publishing important studies performed with up-to-date methodology utilizing sensitive chemical microassays, hybridoma technology, immunocytochemistry, in situ hybridization and receptor radioautography, to name a few examples. The Journal of Chemical Neuroanatomy is the natural vehicle for integrated studies utilizing these approaches. The articles will be selected by the editorial board and invited reviewers on the basis of their excellence and potential contribution to this field of neurosciences. Both in vivo and in vitro integrated studies in chemical neuroanatomy are appropriate subjects of interest to the journal. These studies should relate only to vertebrate species with particular emphasis on the mammalian and primate nervous systems.
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