4.8 Article

Melatonin and probiotics ameliorate nanoplastics-induced hematopoietic injury by modulating the gut microbiotametabolism

期刊

NANO RESEARCH
卷 16, 期 2, 页码 2885-2894

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TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-022-5032-9

关键词

gut microbiota-metabolism; melatonin; probiotics; nanoplastics exposure; hematopoietic injury

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Plastic pollution is a global issue, and nanoplastics can have hematopoietic toxicity. However, supplementation with probiotics and melatonin can mitigate this toxicity, with probiotics being more effective. Interestingly, the interventions may involve different microbes and metabolites.
Plastic pollution has become a non -negligible global pollution problem. Nanoplastics (NP) can reach the bone marrow with blood circulation and develop hematotoxicity, but potential mechanisms and prevention strategies are lacking. Here, we report the biological distribution of NP particles in the bone marrow of mice and hematopoietic toxicity after exposure to 60 mu g of 80 nm NP for 42 days. NP exposure inhibited the capability of bone marrow hematopoietic stem cells to renew and differentiate. Notably, probiotics and melatonin supplementation significantly ameliorated NP-induced hematopoietic damage, and the former was superior to the latter. And interestingly, melatonin and probiotic interventions may involve different microbes and metabolites. After melatonin intervention, creatine showed a stronger correlation with NP-induced gut microbiota disorders. In contrast, probiotic intervention reversed the levels of more gut microbes and plasma metabolites. Of these, threonine, malonylcarnitine, and 3-hydroxybutyric acid might be potential performers in the regulation of hematopoietic toxicity by gut microbes, as they had a more significant relationship with the identified microbes. In conclusion, supplementation with melatonin or probiotics may be two candidates to prevent hematopoietic toxicity attributable to NP exposure, Also, the multi-omits results may lay the foundation for future investigations into in-depth mechanisms.

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