Single but Not Combined In Vitro Exposure to Bisphenol A and Nanoplastics Affects the Cholinergic Function of the Ascidian Ciona robusta.

IF 6.8 Q1 TOXICOLOGY
Safa Melki, Emma Ferrari, Raja Ben Ahmed, Antonietta Spagnuolo, Ilaria Corsi
{"title":"Single but Not Combined In Vitro Exposure to Bisphenol A and Nanoplastics Affects the Cholinergic Function of the Ascidian <i>Ciona robusta</i>.","authors":"Safa Melki, Emma Ferrari, Raja Ben Ahmed, Antonietta Spagnuolo, Ilaria Corsi","doi":"10.3390/jox14040103","DOIUrl":null,"url":null,"abstract":"<p><p>Nanoplastics are known to represent a threat to marine ecosystems. Their combination with other contaminants of emerging concerns (CECs) may amplify ecotoxic effects, with unknown impacts on marine biodiversity. This study investigates the effects, single and combined, of bisphenol A (BPA)-one of the most hazardous CECs-and polystyrene nanoparticles (PS NPs)-as a proxy for nanoplastics, being among the most commonly found asmarine debris-on cholinesterase (ChE) activities of the ascidian <i>Ciona robusta</i>. ChE activity was first measured in the siphons, tunic, and viscera of wild-caught adult specimens and exposed in vitro to BPA (0.01, 0.21, 0.69 mM) and PS NPs (0.0096-0.096 mM; 8.096 × 10<sup>9</sup>-10<sup>10</sup> particles, respectively) alone and combined for 15 min of incubation. PS NPs' behavior in milliQ water and in the ChE assay reaction buffer was characterized alone, combined with BPA, and analyzed through ζ-potential measurements via Dynamic Light Scattering. The results revealed that ChE activity was predominant in the viscera and siphons of <i>C. robusta</i>; PS NPs did not affect the ChE activity alone or combined, while BPA caused a concentration-dependent inhibition of ChE activity in the viscera. No changes in ζ-potential were observed for PS NPs alone or combined with BPA in the ChE buffer, suggesting no interaction. Further investigations are needed to understand the potential neurotoxic consequences for <i>C. robusta</i> and ecological risk scenarios due to exposure to BPA and nanoplastics in marine coastal waters.</p>","PeriodicalId":42356,"journal":{"name":"Journal of Xenobiotics","volume":"14 4","pages":"1930-1940"},"PeriodicalIF":6.8000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11679349/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Xenobiotics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/jox14040103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nanoplastics are known to represent a threat to marine ecosystems. Their combination with other contaminants of emerging concerns (CECs) may amplify ecotoxic effects, with unknown impacts on marine biodiversity. This study investigates the effects, single and combined, of bisphenol A (BPA)-one of the most hazardous CECs-and polystyrene nanoparticles (PS NPs)-as a proxy for nanoplastics, being among the most commonly found asmarine debris-on cholinesterase (ChE) activities of the ascidian Ciona robusta. ChE activity was first measured in the siphons, tunic, and viscera of wild-caught adult specimens and exposed in vitro to BPA (0.01, 0.21, 0.69 mM) and PS NPs (0.0096-0.096 mM; 8.096 × 109-1010 particles, respectively) alone and combined for 15 min of incubation. PS NPs' behavior in milliQ water and in the ChE assay reaction buffer was characterized alone, combined with BPA, and analyzed through ζ-potential measurements via Dynamic Light Scattering. The results revealed that ChE activity was predominant in the viscera and siphons of C. robusta; PS NPs did not affect the ChE activity alone or combined, while BPA caused a concentration-dependent inhibition of ChE activity in the viscera. No changes in ζ-potential were observed for PS NPs alone or combined with BPA in the ChE buffer, suggesting no interaction. Further investigations are needed to understand the potential neurotoxic consequences for C. robusta and ecological risk scenarios due to exposure to BPA and nanoplastics in marine coastal waters.

双酚A和纳米塑料对海鞘胆碱能功能的影响
众所周知,纳米塑料对海洋生态系统构成威胁。它们与其他新出现的污染物(CECs)结合可能会放大生态毒性效应,对海洋生物多样性产生未知的影响。本研究调查了双酚A (BPA)——最危险的ceca之一——和聚苯乙烯纳米颗粒(PS NPs)——作为纳米塑料的替代品(最常见的海洋垃圾之一)对海鞘胆碱酯酶(ChE)活性的影响,单个和组合。首先在野生捕获的成年标本虹吸管、外衣和内脏中测定ChE活性,并在体外暴露于BPA (0.01, 0.21, 0.69 mM)和PS NPs (0.0096-0.096 mM);分别为8.096 × 109-1010粒)单独和联合孵育15分钟。PS NPs在毫克水中和ChE测定反应缓冲液中的行为被单独表征,并与BPA结合,通过动态光散射的ζ电位测量进行分析。结果表明,切酶活性主要分布在黄芪的内脏和虹吸管中;PS NPs不单独或联合影响ChE活性,而BPA引起内脏ChE活性的浓度依赖性抑制。在ChE缓冲液中,单独使用PS NPs或与BPA联合使用PS NPs均未观察到ζ电位的变化,这表明两者之间没有相互作用。需要进一步调查以了解海洋沿海水域暴露于双酚a和纳米塑料对罗布斯塔虫的潜在神经毒性后果和生态风险情景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.30
自引率
1.70%
发文量
21
审稿时长
10 weeks
期刊介绍: The Journal of Xenobiotics publishes original studies concerning the beneficial (pharmacology) and detrimental effects (toxicology) of xenobiotics in all organisms. A xenobiotic (“stranger to life”) is defined as a chemical that is not usually found at significant concentrations or expected to reside for long periods in organisms. In addition to man-made chemicals, natural products could also be of interest if they have potent biological properties, special medicinal properties or that a given organism is at risk of exposure in the environment. Topics dealing with abiotic- and biotic-based transformations in various media (xenobiochemistry) and environmental toxicology are also of interest. Areas of interests include the identification of key physical and chemical properties of molecules that predict biological effects and persistence in the environment; the molecular mode of action of xenobiotics; biochemical and physiological interactions leading to change in organism health; pathophysiological interactions of natural and synthetic chemicals; development of biochemical indicators including new “-omics” approaches to identify biomarkers of exposure or effects for xenobiotics.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信