Carbendazim exposure induces developmental, biochemical and behavioural disturbance in zebrafish embryos
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26653011
DOI
10.1016/j.aquatox.2015.11.017
PII: S0166-445X(15)30099-0
Knihovny.cz E-resources
- Keywords
- Biomarkers, Locomotor response, Sublethal, Swimming behaviour, Zebrafish,
- MeSH
- Benzimidazoles analysis toxicity MeSH
- Water Pollutants, Chemical analysis toxicity MeSH
- Cholinesterases metabolism MeSH
- Behavior, Animal drug effects MeSH
- Zebrafish growth & development physiology MeSH
- Embryo, Nonmammalian drug effects physiology MeSH
- Glutathione Transferase metabolism MeSH
- Carbamates analysis toxicity MeSH
- Catalase metabolism MeSH
- Larva drug effects physiology MeSH
- Locomotion drug effects MeSH
- Swimming MeSH
- Fungicides, Industrial analysis toxicity MeSH
- Tandem Mass Spectrometry MeSH
- Chromatography, High Pressure Liquid MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Benzimidazoles MeSH
- carbendazim MeSH Browser
- Water Pollutants, Chemical MeSH
- Cholinesterases MeSH
- Glutathione Transferase MeSH
- Carbamates MeSH
- Catalase MeSH
- Fungicides, Industrial MeSH
Carbendazim is a widely used broad spectrum benzimidazole fungicide; however, its effects to non-target aquatic organisms are poorly studied. The aim of this study was to investigate the toxic effects of carbendazim to zebrafish early life stages at several levels of biological organization, including developmental, biochemical and behavioural levels. The embryo assay was done following the OECD guideline 236 and using a concentration range between 1.1 and 1.8mg/L. Lethal and developmental endpoints such as hatching, edemas, malformations, heart beat rate, body growth and delays were assessed in a 96h exposure. A sub-teratogenic range (from 0.16 to 500μg/L) was then used to assess effects at biochemical and behavioural levels. Biochemical markers included cholinesterase (ChE), glutathione-S-transferase (GST), lactate dehydrogenase (LDH) and catalase (CAT) and were assessed at 96h. The locomotor behaviour was assessed using an automated video tracking system at 120h. Carbendazim (96h-LC50 of 1.75mg/L) elicited several developmental anomalies in zebrafish embryos with EC50 values ranging from 0.85 to 1.6mg/L. ChE, GST and LDH activities were increased at concentrations equal or above 4μg/L. The locomotor assay showed to be extremely sensitive, detecting effects in time that larvae spent swimming at concentrations of 0.16μg/L and thus, being several orders of magnitude more sensitive that developmental parameters or lethality. These are ecological relevant concentrations and highlight the potential of behavioural endpoints as early warning signs for environmental stress. Further studies should focus on understanding how the behavioural disturbances measured in these types of studies translate into fitness impairment at the adult stage.
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