PUBLICATION
The role of nanoplastics on the toxicity of the herbicide phenmedipham, using Danio rerio embryos as model organisms
- Authors
- Santos, J., Barreto, A., Sousa, É.M.L., Calisto, V., Amorim, M.J.B., Maria, V.L.
- ID
- ZDB-PUB-220323-3
- Date
- 2022
- Source
- Environmental pollution (Barking, Essex : 1987) 303: 119166 (Journal)
- Registered Authors
- Amorim, Monica
- Keywords
- Freshwater fish, Mixtures, Multi-endpoint approach, Pesticides, Plastics
- MeSH Terms
-
- Animals
- Carbamates
- Catalase
- Ecosystem
- Embryo, Nonmammalian
- Glutathione
- Herbicides*/toxicity
- Microplastics
- Transferases/pharmacology
- Water Pollutants, Chemical*/toxicity
- Zebrafish
- PubMed
- 35306087 Full text @ Environ. Pollut.
Citation
Santos, J., Barreto, A., Sousa, É.M.L., Calisto, V., Amorim, M.J.B., Maria, V.L. (2022) The role of nanoplastics on the toxicity of the herbicide phenmedipham, using Danio rerio embryos as model organisms. Environmental pollution (Barking, Essex : 1987). 303:119166.
Abstract
Once in the aquatic ecosystems, nanoplastics (NPls) can interact with other contaminants acting as vectors of transport and altering their toxicological effects towards organisms. Thus, the present study aims to investigate how polystyrene NPls (44 nm) interact with the herbicide phenmedipham (PHE) and affect its toxicity to zebrafish embryos. Single exposures to 0, 0.015, 0.15, 1.5, 15 and 150 mg/L NPls and 0.02, 0.2, 2 and 20 mg/L PHE were performed. Embryos were also exposed to the binominal combinations: 0.015 mg/L NPls +2 mg/L PHE, 0.015 mg/L NPls +20 mg/L PHE, 1.5 mg/L NPls +2 mg/L PHE and 1.5 mg/L NPls +20 mg/L PHE. Due to the low solubility of PHE in water, a solvent control was performed (0.01% acetone). PHE was quantified. Mortality, heartbeat and hatching rate, malformations appearance, locomotor behavior and biomarkers related to oxidative stress, neurotransmission and energy budgets were analyzed. During 96 h, NPls and PHE single and combined exposures did not affect embryos development. After 120 h, NPls induced hyperactivity and PHE induced hypoactivity. After 96 h, NPls increased catalase activity and PHE increased glutathione S-transferases activity. On the combination 0.015 mg/L NPls +20 mg/L PHE, hyperactivity behavior was found, similar to 0.015 mg/L NPls, and cholinesterase activity was inhibited. Additionally, the combination 1.5 mg/L NPls +20 mg/L PHE increased both catalase and glutathione S-transferases activities. The combination NPls with PHE affected more biochemical endpoints than the single exposures, showing the higher effect of the binominal combinations. Dissimilar interactions effects - no interaction, synergism and antagonism - between NPls and PHE were found. The current study shows that the effects of NPls on bioavailability and toxicity of other contaminants (e.g. PHE) cannot be ignored during the assessment of NPls environmental behavior and risks.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping