4.7 Article

Environmental levels of carbaryl impair zebrafish larvae behaviour: The potential role of ADRA2B and HTR2B

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 431, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.128563

Keywords

Carbaryl; Zebrafish; Behaviour; Acetylcholinesterase; ADRA2B; HTR2B

Funding

  1. Agencia Estatal de Investigacion from the Spanish Ministry of Science and Innovation [PID2020-113371RB-C21]
  2. IDAEA-CSIC, Severo Ochoa Centre of Excellence [CEX2018-000794-S]
  3. Severo Ochoa funds
  4. Spanish Government [PRE2018-083513]
  5. European Social Fund (ESF)
  6. Ministerio de Ciencia e Innovacion, Agencia Estatal de Investigacion and ERDF-FEDER European Fund [CTQ2017-89222-R, PID2020-120499RB-I00]
  7. Catalan Government [2017 SGR 1604, 2017-SGR-1807]
  8. Spanish Ministry of Economy, Industry and Competitiveness [SAF2015-74132-JIN]

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This study reveals the adverse effects of the insecticide carbaryl on the behavior of zebrafish larvae and demonstrates that the antagonistic interactions of carbaryl with ADRA2B and HTR2B receptors are the molecular initiating events leading to these effects.
The insecticide carbaryl is commonly found in indirectly exposed freshwater ecosystems at low concentrations considered safe for fish communities. In this study, we showed that after only 24 h of exposure to environmental concentrations of carbaryl (0.066-660 ng/L), zebrafish larvae exhibit impairments in essential behaviours. Interestingly, the observed behavioural effects induced by carbaryl were acetylcholinesterase-independent. To elucidate the molecular initiating event that resulted in the observed behavioural effects, in silico predictions were followed by in vitro validation. We identified two target proteins that potentially interacted with carbaryl, the alpha 2B adrenoceptor (ADRA2B) and the serotonin 2B receptor (HTR2B). Using a pharmacological approach, we then tested the hypothesis that carbaryl had antagonistic interactions with both receptors. Similar to yohimbine and SB204741, which are prototypic antagonists of ADRA2B and HTR2B, respectively, carbaryl increased the heart rate of zebrafish larvae. When we compared the behavioural effects of a 24-h exposure to these pharmacological antagonists with those of carbaryl, a high degree of similarity was found. These results strongly suggest that antagonism of both ADRA2B and HTR2B is the molecular initiating event that leads to adverse outcomes in zebrafish larvae that have undergone 24 h of exposure to environmentally relevant levels of carbaryl.

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