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Co-exposure with cadmium elevates the toxicity of microplastics: Trojan horse effect from the perspective of intestinal barrier

Journal of Hazardous Materials 2024 72 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 70 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Liehai Hu, Xiaoyan Feng, Yuzhi Lan, Yuzhi Lan, Yuzhi Lan, Yuzhi Lan, Liehai Hu, Penghui Nie, Yuzhi Lan, Yuzhi Lan, Yuzhi Lan, Liehai Hu, Yuzhi Lan, Xiaoyan Feng, Penghui Nie, Xiaoyan Feng, Penghui Nie, Penghui Nie, Yuzhi Lan, Penghui Nie, Penghui Nie, Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Xiaoyan Feng, Xiaoyan Feng, Liehai Hu, Yuzhi Lan, Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Jingfeng Zhang, Liehai Hu, Hengyi Xu Penghui Nie, Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu Hengyi Xu

Summary

When mice were exposed to both microplastics and the toxic metal cadmium together, the health damage to their intestines and liver was significantly worse than exposure to either pollutant alone. The microplastics acted like a "Trojan horse," carrying cadmium past the gut barrier and increasing its accumulation in the body, while also disrupting the gut microbiome.

Microplastics (MPs) have been shown to adsorb heavy metals and serve as vehicles for their environmental transport. To date, insufficient studies have focused on enterohepatic injury in mice co-exposed to both MPs and cadmium (Cd). Here, we report that Cd adsorption increased the surface roughness and decreased the monodispersity of PS-MPs. Furthermore, exposure to both PS-MPs and Cd resulted in a more severe toxic effect compared to single exposure, with decreased body weight gain, shortened colon length, and increased colonic and hepatic inflammatory response observed. This can be attributed to an elevated accumulation of Cd resulting from increased gut permeability, coupled with the superimposed effects of oxidative stress. In addition, using 16 S sequencing and fecal microbiota transplantation, it was demonstrated that gut microbiota dysbiosis plays an essential role in the synergistic toxicity induced by PS-MPs and Cd in mice. This study showed that combined exposure to MPs and Cd induced more severe intestinal and liver damage in mice compared to individual exposure, and provided a new perspective for a more systematic risk assessment process related to MPs exposure.

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