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Polystyrene microplastics induce mortality through acute cell stress and inhibition of cholinergic activity in a brine shrimp
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Researchers exposed brine shrimp to polystyrene microplastics and found that even small particles trigger rapid cell stress and disrupt the nervous system by inhibiting cholinergic activity, suggesting microplastics can kill aquatic invertebrates through mechanisms that may also be relevant to other animals.
The environmental impacts of microplastics (MPs) are increasingly of concern, particularly for their sources, global distribution, and persistency in aquatic ecosystems. Although the ubiquitous and persistent nature of MPs in waterbodies is evident, their effects and health implications for aquatic animals are still open to debate. The brine shrimp, Artemia franciscana was exposed to different concentrations (1–1000 particles mL−1) of four sizes (1, 3, 6, and 10 μm) of non-functionalized polystyrene microbeads. To measure MPs effects, several physiological and biochemical parameters such as ingestion and egestion, stress biomarkers [e.g., heat shock protein 70 (hsp70) family, enzymatic activities of catalase (CAT) and superoxide dismutase (SOD)], acetylcholinesterase (AChE) activity, and survival rate for 30 days were analyzed. Exposure to waterborne MPs showed clear ingestion and egestion in A. franciscana. Exposure to relatively larger sizes of 1000 particles mL−1 MPs dose–dependently increased mRNA expression of hsp70 families and enzymatic activities of CAT and SOD within 96 h. Significant inhibitory effects on AChE activity were observed in response to 1000 particles mL−1 with increases in mortality for 30 days. Thirty-day survival of juveniles was dose-dependently affected, with greater effects seen at 1000 particles mL−1 of MPs. Our results suggest that MPs exposure to the early stages of brine shrimp could be detrimental for population maintenance through inhibition of cholinergic system and the induction of acute cell stress, including oxidative stress.
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Researchers exposed brine shrimp to polystyrene microbeads of three sizes and found that smaller particles (0.05 micrometers) caused greater oxidative stress, mitochondrial damage, and gut cell apoptosis via the p53-Bax-Bcl2 signaling pathway, demonstrating that microplastic toxicity in aquatic organisms is size-dependent.
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Acute and chronic effects of polystyrene microplastics on brine shrimp: First evidence highlighting the molecular mechanism through transcriptome analysis
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Researchers investigated both acute and chronic toxicity of polystyrene microplastics on brine shrimp, using transcriptome analysis to uncover molecular mechanisms. While acute exposure did not significantly affect survival, chronic exposure led to concentration-dependent bioaccumulation and increased reactive oxygen species generation, with gene expression analysis revealing disrupted metabolic and stress response pathways.
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Scientists found that tiny plastic particles (nanoplastics) can damage the immune cells of oysters by harming their mitochondria, the "batteries" that power cells, leading to DNA damage even at low exposure levels. While this study was done in oysters, not humans, it adds to growing evidence that nanoplastics can disrupt basic cell functions, raising questions about what similar exposure might mean for human health given how widespread plastic pollution has become in our food and water.
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