Tianyu Zhao , Yuping Zhang , Qianqian Song , Qingxuan Meng , Xinrui Meng , Xiaolong Wang , Jing Cong
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Chemical analyses identified elevated levels of heavy metals and biologically active organic compounds in LAP leachate, including higher zinc concentrations and benzothiazole derivatives, likely contributing to its greater toxicity. Oxidative stress markers revealed that LAP exposure induced a 1.46-fold increase in malondialdehyde (MDA) and suppressed glutathione S-transferase (GST) activity (31.6 % reduction), indicating impaired detoxification. Transcriptomics identified ferroptosis as a central putative toxicity pathway: LAP exposure was associated with dysregulated iron metabolism genes (<em>mt2</em>↑, <em>fthl31</em>↑, <em>slc40a1</em>↓), and an exacerbation of lipid peroxidation, whereas TWP exposure was linked to adaptive responses via <em>cyp1a</em> and <em>gstt1b</em> upregulation. Functional rescue experiments using ferrostatin-1 further supported the involvement of ferroptosis, showing consistent but non-significant trends of physiological mitigation. These findings highlight distinct mechanistic pathways: LAP exposure correlated with pathways consistent with iron dyshomeostasis-driven ferroptosis, while TWP exposure appeared to induce phase I/II detoxification, providing molecular insights into microrubber toxicity. The study underscores the urgent need for source-specific risk assessments and regulatory measures to mitigate microrubber pollution in aquatic ecosystems.</div></div>","PeriodicalId":10602,"journal":{"name":"Comparative Biochemistry and Physiology C-toxicology & Pharmacology","volume":"297 ","pages":"Article 110285"},"PeriodicalIF":3.9000,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Environmental toxicity of tire wear and latex particle leachates in zebrafish embryos: Oxidative stress and ferroptosis as key mechanisms\",\"authors\":\"Tianyu Zhao , Yuping Zhang , Qianqian Song , Qingxuan Meng , Xinrui Meng , Xiaolong Wang , Jing Cong\",\"doi\":\"10.1016/j.cbpc.2025.110285\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Microrubber, a subset of microplastics, has raised global concerns due to its persistence and ecological risks in aquatic systems. This study systematically compared the toxicity of leachates (0, 0.5, 2.5, 5, 7.5, and 10 g/L) from tire wear particles (TWP) and latex particles (LAP) in zebrafish embryos for 5 days, integrating physiological endpoints, oxidative stress biomarkers, and transcriptomic profiling. LAP leachate exhibited significantly higher toxicity than TWP, causing increased mortality (100 % vs. 56.3 %), delayed hatching (0 % vs. 35.4 %), and severe malformations (e.g., tail and spine curvature). Chemical analyses identified elevated levels of heavy metals and biologically active organic compounds in LAP leachate, including higher zinc concentrations and benzothiazole derivatives, likely contributing to its greater toxicity. Oxidative stress markers revealed that LAP exposure induced a 1.46-fold increase in malondialdehyde (MDA) and suppressed glutathione S-transferase (GST) activity (31.6 % reduction), indicating impaired detoxification. Transcriptomics identified ferroptosis as a central putative toxicity pathway: LAP exposure was associated with dysregulated iron metabolism genes (<em>mt2</em>↑, <em>fthl31</em>↑, <em>slc40a1</em>↓), and an exacerbation of lipid peroxidation, whereas TWP exposure was linked to adaptive responses via <em>cyp1a</em> and <em>gstt1b</em> upregulation. Functional rescue experiments using ferrostatin-1 further supported the involvement of ferroptosis, showing consistent but non-significant trends of physiological mitigation. These findings highlight distinct mechanistic pathways: LAP exposure correlated with pathways consistent with iron dyshomeostasis-driven ferroptosis, while TWP exposure appeared to induce phase I/II detoxification, providing molecular insights into microrubber toxicity. 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引用次数: 0
摘要
微橡胶是微塑料的一个子集,由于其在水生系统中的持久性和生态风险,引起了全球关注。本研究系统地比较了轮胎磨损颗粒(TWP)和乳胶颗粒(LAP)的渗滤液(0、0.5、2.5、5、7.5和10 g/L)对斑马鱼胚胎的毒性,并整合了生理终点、氧化应激生物标志物和转录组学分析。LAP渗滤液的毒性明显高于TWP,导致死亡率增加(100% vs. 56.3%),孵化延迟(0% vs. 35.4%)和严重畸形(如尾巴和脊柱弯曲)。化学分析发现,LAP渗滤液中重金属和生物活性有机化合物水平升高,包括锌浓度升高和苯并噻唑衍生物,这可能导致其毒性更大。氧化应激标志物显示,LAP暴露诱导丙二醛(MDA)增加1.46倍,抑制谷胱甘肽s -转移酶(GST)活性(降低31.6%),表明解毒受损。转录组学鉴定铁死亡是一种中心的毒性途径:LAP暴露与铁代谢基因失调(mt2↑,fthl31↑,slc40a1↓)和脂质过氧化加剧有关,而TWP暴露通过cyp1a和gstt1b上调与适应性反应有关。使用他汀-1的功能挽救实验进一步支持了铁下垂的参与,显示出一致但不显著的生理缓解趋势。这些发现强调了不同的机制途径:LAP暴露与铁失衡驱动的铁凋亡相关,而TWP暴露似乎诱导I/II期解毒,为微橡胶毒性提供了分子见解。该研究强调,迫切需要针对特定来源进行风险评估和采取监管措施,以减轻水生生态系统中的微橡胶污染。
Environmental toxicity of tire wear and latex particle leachates in zebrafish embryos: Oxidative stress and ferroptosis as key mechanisms
Microrubber, a subset of microplastics, has raised global concerns due to its persistence and ecological risks in aquatic systems. This study systematically compared the toxicity of leachates (0, 0.5, 2.5, 5, 7.5, and 10 g/L) from tire wear particles (TWP) and latex particles (LAP) in zebrafish embryos for 5 days, integrating physiological endpoints, oxidative stress biomarkers, and transcriptomic profiling. LAP leachate exhibited significantly higher toxicity than TWP, causing increased mortality (100 % vs. 56.3 %), delayed hatching (0 % vs. 35.4 %), and severe malformations (e.g., tail and spine curvature). Chemical analyses identified elevated levels of heavy metals and biologically active organic compounds in LAP leachate, including higher zinc concentrations and benzothiazole derivatives, likely contributing to its greater toxicity. Oxidative stress markers revealed that LAP exposure induced a 1.46-fold increase in malondialdehyde (MDA) and suppressed glutathione S-transferase (GST) activity (31.6 % reduction), indicating impaired detoxification. Transcriptomics identified ferroptosis as a central putative toxicity pathway: LAP exposure was associated with dysregulated iron metabolism genes (mt2↑, fthl31↑, slc40a1↓), and an exacerbation of lipid peroxidation, whereas TWP exposure was linked to adaptive responses via cyp1a and gstt1b upregulation. Functional rescue experiments using ferrostatin-1 further supported the involvement of ferroptosis, showing consistent but non-significant trends of physiological mitigation. These findings highlight distinct mechanistic pathways: LAP exposure correlated with pathways consistent with iron dyshomeostasis-driven ferroptosis, while TWP exposure appeared to induce phase I/II detoxification, providing molecular insights into microrubber toxicity. The study underscores the urgent need for source-specific risk assessments and regulatory measures to mitigate microrubber pollution in aquatic ecosystems.
期刊介绍:
Part C: Toxicology and Pharmacology. This journal is concerned with chemical and drug action at different levels of organization, biotransformation of xenobiotics, mechanisms of toxicity, including reactive oxygen species and carcinogenesis, endocrine disruptors, natural products chemistry, and signal transduction with a molecular approach to these fields.