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氧化/未修饰的聚乙烯微塑料对小鼠的神经毒性:从微生物群-肠道-大脑轴的角度来看。

Oxidized/unmodified-polyethylene microplastics neurotoxicity in mice: Perspective from microbiota-gut-brain axis.

机构信息

School of Life Sciences, Lanzhou University, No. 222 South Tianshui Road, Lanzhou 730000, Gansu Province, China.

School of Life Sciences, Lanzhou University, No. 222 South Tianshui Road, Lanzhou 730000, Gansu Province, China; NHC Key Laboratory of Diagnosis and Therapy of Gastrointestinal Tumor, Gansu Provincial Hospital, Lanzhou 730000, Gansu Province, China.

出版信息

Environ Int. 2024 Mar;185:108523. doi: 10.1016/j.envint.2024.108523. Epub 2024 Mar 7.

Abstract

Microplastics (MPs) are inevitably oxidized in the environment, and their potential toxicity to organisms has attracted wide attention. However, the neurotoxicity and mechanism of oxidized polyethylene (Ox-PE) MPs to organisms remain unclear. Herein, we prepared oxidized low-density polyethylene (Ox-LDPE) and established a model of MPs exposure by continuously orally gavage of C57BL/6 J mice with LDPE-MPs/Ox-LDPE-MPs for 28 days with or without oral administration of Lactobacillus plantarum DP189 and galactooligosaccharides (DP189&GOS). The experimental results indicated that LDPE-MPs or Ox-LDPE-MPs caused several adverse effects in mice, mainly manifested by behavioral changes, disruption of the intestinal and blood-brain barrier (BBB), and simultaneous oxidative stress, inflammatory reactions, and pathological damage in the brain and intestines. Brain transcriptomic analysis revealed that the cholinergic synaptic signaling pathways, which affect cognitive function, were significantly disrupted after exposure to LDPE-MPs or Ox-LDPE-MPs. Real-time quantitative polymerase chain reaction and Western Blotting results further demonstrated that the critical genes (Slc5a7, Chat and Slc18a3) and proteins (Chat and Slc18a3) in the cholinergic synaptic signaling pathway were significantly down-regulated after exposure to LDPE-MPs or Ox-LDPE-MPs. These alterations lead to reduced acetylcholine concentration, which causes cognitive dysfunction in mice. Importantly, the DP189&GOS interventions effectively mitigated the MPs-induced cognitive dysfunction and intestinal microbiota alteration, improved intestinal and BBB integrity, attenuated the oxidative stress and inflammatory response, and also saw a rebound in the release of acetylcholine. These results indicated that LDPE-MPs and Ox-LDPE-MPs exert neurotoxic effects on mice by inducing oxidative stress, inflammatory responses, and dysregulation of cholinergic signaling pathways in the mouse brain. That probiotic supplementation is effective in attenuating MPs-induced neurotoxicity in mice. Overall, this study reveals the potential mechanisms of neurotoxicity of LDPE-MPs and Ox-LDPE-MPs on mice and their improvement measures, necessary to assess the potential risks of plastic contaminants to human health.

摘要

微塑料(MPs)在环境中不可避免地会被氧化,其对生物体的潜在毒性引起了广泛关注。然而,氧化聚乙烯(Ox-PE) MPs 对生物体的神经毒性及其机制仍不清楚。本研究中,我们制备了氧化低密度聚乙烯(Ox-LDPE),并通过连续口服灌胃 C57BL/6 J 小鼠 LDPE-MPs/Ox-LDPE-MPs 28 天,建立 MPs 暴露模型,同时给予植物乳杆菌 DP189 和半乳糖低聚糖(DP189&GOS)口服干预。实验结果表明,LDPE-MPs 或 Ox-LDPE-MPs 导致小鼠出现多种不良效应,主要表现为行为改变、肠道和血脑屏障(BBB)破坏,以及脑和肠道同时发生氧化应激、炎症反应和病理性损伤。脑转录组分析显示,暴露于 LDPE-MPs 或 Ox-LDPE-MPs 后,影响认知功能的胆碱能突触信号通路明显受到干扰。实时定量聚合酶链反应和 Western Blotting 结果进一步表明,暴露于 LDPE-MPs 或 Ox-LDPE-MPs 后,胆碱能突触信号通路中的关键基因(Slc5a7、Chat 和 Slc18a3)和蛋白(Chat 和 Slc18a3)显著下调。这些改变导致乙酰胆碱浓度降低,从而导致小鼠认知功能障碍。重要的是,DP189&GOS 干预可有效减轻 MPs 引起的认知功能障碍和肠道微生物群改变,改善肠道和 BBB 完整性,减轻氧化应激和炎症反应,并使乙酰胆碱的释放恢复。这些结果表明,LDPE-MPs 和 Ox-LDPE-MPs 通过诱导小鼠大脑中的氧化应激、炎症反应和胆碱能信号通路失调,对小鼠产生神经毒性作用。补充益生菌可有效减轻 MPs 诱导的小鼠神经毒性。总之,本研究揭示了 LDPE-MPs 和 Ox-LDPE-MPs 对小鼠产生神经毒性的潜在机制及其改善措施,这对于评估塑料污染物对人类健康的潜在风险是必要的。

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