Synergistic Mitochondrial Genotoxicity of Carbon Dots and Arsenate in Earthworms Eisenia fetida across Generations: The Critical Role of Binding.
Yuhan DengMin JiangMao WangKewei RenXia LuoYan LuoQing ChenChensheng Alex LuCheng Zhi HuangQingqing LiuPublished in: Environmental science & technology (2024)
The escalating utilization of carbon dots (CDs) in agriculture raises ecological concerns. However, their combined toxicity with arsenic remains poorly understood. Herein, we investigated the combined mitochondrial genotoxicity of CDs and arsenate at environmentally relevant concentrations across successive earthworm generations. Iron-doped CDs (CDs -Fe ) strongly bound to arsenate and arsenite, while nitrogen-doped CDs (CDs -N ) exhibited weaker binding. Both CDs enhanced arsenate bioaccumulation without affecting its biotransformation, with most arsenate being reduced to arsenite. CDs -Fe generated significantly more reactive oxygen species than did CDs -N , causing stronger mitochondrial DNA (mtDNA) damage. Arsenate further exacerbated the oxidative mtDNA damage induced by CDs -N , as evidenced by increased reactive oxygen species, elevated 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-OHdG) levels, and a higher correlation between 8-OHdG and mtDNA damage. This was due to arsenic inhibiting the antioxidant enzyme catalase. This exacerbation was negligible with CDs -Fe because their strong binding with arsenic prevented catalase inhibition. Maternal mitochondrial DNA damage was inherited by filial earthworms, which experienced significant weight loss in coexposure groups coupled with mtDNA toxicity. This study reveals the synergistic genotoxicity of CDs and arsenate, suggesting that CDs could disrupt the arsenic biogeochemical cycle, increase arsenate risk to terrestrial animals, and influence ecosystem stability and health through multigenerational impacts.
Keyphrases
- quantum dots
- visible light
- mitochondrial dna
- oxidative stress
- copy number
- reactive oxygen species
- dna damage
- heavy metals
- drinking water
- weight loss
- climate change
- healthcare
- type diabetes
- gene expression
- chronic obstructive pulmonary disease
- human health
- dna methylation
- cancer therapy
- dna binding
- health information
- health risk
- genome wide
- oxide nanoparticles
- gastric bypass
- health risk assessment
- birth weight
- social media