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Chronic exposure to UV-aged microplastics induces neurotoxicity by affecting dopamine, glutamate, and serotonin neurotransmission in Caenorhabditis elegans
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Researchers found that UV-aged microplastics caused more severe neurotoxic effects than pristine microplastics when worms were chronically exposed to low concentrations. The aged particles disrupted dopamine, glutamate, and serotonin signaling pathways and caused visible neurodegeneration in the test organisms. The study suggests that microplastics become more harmful as they weather in the environment, which is an important consideration for assessing real-world exposure risks.
Microplastics are ubiquitous in all environments and exert toxic effects in various organisms. However, the neurotoxicity and underlying mechanisms of long-term exposure to MPs aged under UV radiation remain largely unclear. In this study, Caenorhabditis elegans was treated with 0.1-100 μg/L virgin and aged polystyrene microplastics (PS-MPs) for 10 d, with locomotion behavior, neuronal development, neurotransmitter content, and neurotransmission-related to gene expression as endpoints. Using locomotion behavior as an endpoint, chronic exposure to aged PS-MPs at low concentrations (1 μg/L) caused more severe neurotoxicity than that to virgin PS-MPs. In transgenic nematodes, exposure to 10-100 μg/L aged PS-MPs significantly influenced the fluorescence intensity and percentage of worms with neurodegeneration of dopaminergic, glutamatergic, and serotonergic neurons compared with control. Further investigations showed that the content of glutamate, serotonin, and dopamine was significantly influenced in nematodes chronically exposed to 100 μg/L of aged PS-MPs. Similarly, neurotransmission-related gene (e.g., eat-4, dat-1, and tph-1) expression was also altered in nematodes. These results indicate that aged PS-MPs exert neurotoxicity owing to their effects on dopamine, glutamate, and serotonin neurotransmission. This study provides insights into the underlying mechanisms and potential risks of PS-MPs after UV radiation.
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Photoaged microplastics induce neurotoxicity associated with damage to serotonergic, glutamatergic, dopaminergic, and GABAergic neuronal systems in Caenorhabditis elegans
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Researchers found that sunlight-aged microplastics caused more severe brain and nerve damage than fresh microplastics in lab worms, disrupting four major neurotransmitter systems: serotonin, glutamate, dopamine, and GABA. Even at very low, environmentally realistic concentrations, the aged particles impaired movement and altered gene expression related to nerve signaling. Since most microplastics in the real world have been weathered by sunlight, this study suggests that the neurotoxic risks of environmental microplastic exposure may be greater than studies using pristine particles indicate.
UV-aged microplastics induces neurotoxicity by affecting the neurotransmission in larval zebrafish
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Researchers compared the neurotoxic effects of fresh versus UV-aged polystyrene microplastics on zebrafish larvae. They found that aged microplastics caused more severe behavioral changes and significantly altered levels of key brain chemicals including dopamine, serotonin, and acetylcholine. The study demonstrates that environmental weathering makes microplastics more neurotoxic, which is an important consideration for assessing the real-world risks of plastic pollution in aquatic ecosystems.
Photoaged Nanopolystyrene Affects Neurotransmission to Induce Transgenerational Neurotoxicity in Caenorhabditis elegans
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When tiny roundworms were exposed to sunlight-aged nanoplastics, their offspring showed movement problems and damaged nerve cells for up to two generations, even without further exposure. The aged nanoplastics were more harmful than fresh ones and worked by disrupting key brain chemicals like dopamine and serotonin, suggesting that weathered plastic particles in the environment may pose greater risks to nervous system health across generations.
Neurotoxicity induced by aged microplastics from plastic bowls: Abnormal neurotransmission in Caenorhabditis elegans
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Researchers found that microplastics released from aged plastic bowls caused nerve damage in the roundworm C. elegans at environmentally realistic concentrations. The aged microplastics disrupted neurotransmitter systems including dopamine and serotonin, leading to impaired movement. This study is concerning because it shows that everyday plastic items we use for food can release microplastics that have neurotoxic effects.
Environmentally persistent free radicals on photoaged nanopolystyrene induce neurotoxicity by affecting dopamine, glutamate, serotonin and GABA in Caenorhabditis elegans
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Researchers found that when polystyrene nanoplastics age under sunlight, they generate environmentally persistent free radicals on their surface that make them significantly more toxic to the nervous system. Using the model organism C. elegans, they showed that aged nanoplastics disrupted movement and reduced levels of key neurotransmitters including dopamine, serotonin, and GABA. The study suggests that weathered nanoplastics in the environment may pose greater neurological risks than freshly produced particles.
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