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Evidence that microplastics aggravate the toxicity of organophosphorus flame retardants in mice (Mus musculus)
Yongfeng Deng1, Yan Zhang1, Ruxia Qiao1
1State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China.
Abstract:
This study was performed to reveal the health risks of co-exposure to organophosphorus flame retardants (OPFRs) and microplastics (MPs). We exposed mice to polyethylene (PE) and polystyrene (PS) MPs and OPFRs [tris (2-chloroethy) phosphate (TCEP) and tris (1,3-dichloro-2-propyl) phosphate (TDCPP)] for 90 days. Biochemical markers and metabolomics were used to determine whether MPs could enhance the toxicity of OPFRs. Superoxide dismutase (SOD) and catalase (CAT) increased (p < 0.05) by 21% and 26% respectively in 10 μg/L TDCPP + PE group compared to TDCPP group. Lactate dehydrogenase (LDH) in TDCPP + MPs groups were higher (18%-30%) than that in TDCPP groups (p < 0.05). Acetylcholinesterase (AChE) in TCEP + PE groups were lower (10%-19%) than those in TCEP groups (p < 0.05). These results suggested that OPFR co-exposure with MPs induced more toxicity than OPFR exposure alone. Finally, in comparison to controls we observed that 29, 41, 41, 26, 40 and 37 metabolites changed significantly (p < 0.05; fold-change > 1.2) in TCEP, TCEP + PS, TCEP + PE, TDCPP, TDCPP + PS and TDCPP + PE groups, respectively. Most of these metabolites are related to pathways of amino acid and energy metabolism. Our results indicate that MPs aggravate the toxicity of OPFRs and highlight the health risks of MP co-exposure with other pollutants.
Insights
Co-exposure to microplastics (MPs) and organophosphorus flame retardants (OPFRs) like TCEP and TDCPP in mice significantly increased toxicity. MPs aggravate OPFR health risks, impacting amino acid and energy metabolism.
Area of Science:
- Environmental Toxicology
- Chemical Health Risks
- Metabolomics
Background:
- Organophosphorus flame retardants (OPFRs) are widely used, raising concerns about their environmental persistence and health effects.
- Microplastics (MPs) are ubiquitous environmental contaminants with incompletely understood toxicological impacts.
- The combined effects of co-exposure to OPFRs and MPs on health remain largely uncharacterized.
Purpose of the Study:
- To investigate the health risks associated with co-exposure to OPFRs (TCEP, TDCPP) and common MPs (polyethylene, polystyrene) in a mouse model.
- To determine if MPs enhance the toxicity of OPFRs using biochemical markers and metabolomic profiling.
- To elucidate the metabolic pathways affected by combined OPFR and MP exposure.
Main Methods:
- Mice were exposed to OPFRs (TCEP, TDCPP) and MPs (PE, PS) individually and in combination for 90 days.
- Biochemical markers including superoxide dismutase (SOD), catalase (CAT), lactate dehydrogenase (LDH), and acetylcholinesterase (AChE) were analyzed.
- Untargeted metabolomics was employed to identify and quantify changes in metabolite profiles.
Main Results:
- Co-exposure to OPFRs and MPs resulted in significantly altered biochemical markers compared to OPFR exposure alone.
- Elevated LDH levels were observed in TDCPP + MP groups, while AChE levels decreased in TCEP + PE groups.
- Significant changes in 26-41 metabolites, primarily related to amino acid and energy metabolism, were detected in co-exposed groups.
Conclusions:
- Microplastics exacerbate the toxicity of organophosphorus flame retardants.
- Combined exposure to OPFRs and MPs poses significant health risks, affecting critical metabolic pathways.
- Further research is warranted to understand the long-term health implications of co-exposure to these environmental contaminants.
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