Toxic effects of oxine-copper on development and behavior in the embryo-larval stages of zebrafish
Creators
- 1. Center for Developmental Biology of Jinggangshan University, College of Life Sciences, Jinggangshan University, Ji'an, Jiangxi (China)
- 2. Jiangxi Engineering Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases, Jiangxi Key Laboratory of Developmental Biology of Organs, Ji'an, Jiangxi (China)
- 3. Department of Ultrasound, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, 330006 (China)
- 4. Department of General Surgery, Jiangxi Provincial Children's Hospital, Nanchang 330006 (China)
Description
Highlights: • Oxine-copper induced abnormalities of head and trunk of embryos and behavioral changes of larvae. • Oxine-copper led to oxidative stress, decreased AChE activity and increased apoptosis. • Oxine-copper exposure changed the expression of genes involved in neurodevelopment, vascular development and apoptosis. • Oxine-copper exposure resulted in neurotoxicity and toxicity to vascular development. -- Abstract: Oxine-copper (OxCu) is generally used as an agricultural pesticide and induces harmful effects on ecosystems. In this study, zebrafish was used to assess the aquatic toxicity of OxCu. To detect the effects on development, embryos of 6 h post-fertilization (hpf) were exposed to 10 μg/L, 20 μg/L, 40 μg/L OxCu for 18 h; meanwhile, to evaluate the effects on the behavior, larval fish at 6 days post-fertilization (dpf) were exposed to the same concentrations for 24 h. Here, we show that there are embryonic developmental defects, including abnormalities of head and trunk, brain ventricle atrophy, reduced newborn neurons, disordered neurons, increased intercellular space, concentrated cytoplasm, decreased heart beat and blood flow velocity, and developmental delay of the vascular system; in addition, some embryos exposed to the high concentration of OxCu degraded from the tail. We also found that the spontaneous tail coiling frequency and AChE enzyme activity were reduced, while oxidative stress (free radical damage) and cell apoptosis were significantly increased. Moreover, the expression of genes involved in neurodevelopment, vascular development and apoptosis were dysregulated in the OxCu exposed embryos in a concentration-dependent manner. Finally, we found that after exposure to OxCu, larval locomotor activity was decreased and accompanied by Parkinson-like (increased absolute turn angle and sinuosity) and anxiety-like (preferred to the central area) behavior. These results indicate that OxCu induces developmental toxicity and behavioral alterations by affecting AChE enzyme activity and oxidative stress. Our data present new proofs of OxCu toxicity and a warning for its application.
Additional details
Identifiers
- DOI
- 10.1016/j.aquatox.2019.02.020;
- PII
- S0166445X18311342;
Publishing Information
- Journal Title
- Aquatic Toxicology
- Journal Volume
- 210
- Journal Page Range
- p. 242-250
- ISSN
- 0166-445X
- CODEN
- AQTODG
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55044384
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- APOPTOSIS; ATROPHY; CYTOPLASM; ECOLOGICAL CONCENTRATION; ECOSYSTEMS; EMBRYOS; ENZYME ACTIVITY; FERTILIZATION; LARVAE; NEONATES; NERVE CELLS; OXIDATION; OXINE; PESTICIDES
- Descriptors DEC
- ANIMAL CELLS; ANIMALS; AROMATICS; AZAARENES; AZINES; CELL CONSTITUENTS; CHEMICAL REACTIONS; HETEROCYCLIC COMPOUNDS; HYDROCARBONS; HYDROXY COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PATHOLOGICAL CHANGES; PYRIDINES; QUINOLINES; SOMATIC CELLS
Optional Information
- Copyright
- Copyright (c) 2019 Elsevier B.V. All rights reserved.