Acute thiamethoxam exposure induces hepatotoxicity and neurotoxicity in juvenile Chinese mitten crab (Eriocheir sinensis)

作者：Yang, Yiwen; Yu, Qiuran; Zhang, Cong; Wang, Xiaodan; He, Long; Huang, Yuxing; Li, Erchao; Qin, Jianguang; Chen, Liqiao^*

来源：Ecotoxicology and Environmental Safety, 2023, 249: 114399.

DOI：10.1016/j.ecoenv.2022.114399

• Neonicotinoid pesticides
• Crustacean
• Oxidative stress
• Detoxification
• Synaptic transmission
• Toxicity

The similar nervous system structure between crustaceans and insects and the high-water solubility of thiame-thoxam can lead to the more severe toxicity of thiamethoxam to crustaceans. However, the effects of thiame-thoxam on crustaceans are unclear. Therefore, a 96-h acute toxicity test was performed to explore the hepatotoxicity and neurotoxicity effects of thiamethoxam on Chinese mitten crab (Eriocheir sinensis) at con-centrations 0 mu g/L, 150 mu g/L and 300 mu g/L. The antioxidant and detoxification systems (including phases I and II) were significantly activated after exposure of juvenile crabs to thiamethoxam for 24 h in 300 mu g/L group, whereas the toxic activation effect in 150 mu g/L group was delayed. Moreover, a similar pattern was observed for the transcription levels of immune-related genes. Further analysis of inflammatory signaling pathway-related genes showed that thiamethoxam exposure with 300 mu g/L for 24 h may induce a pro-inflammatory response through the NF-kappa B pathway. In contrast, the gene expression levels in 150 mu g/L group were significantly upre-gulated compared with 0 mu g/L group after 96 h. In addition, although the acute exposure of 150 mu g/L thiame-thoxam did not seem to induce significant neurotoxicity, the acetylcholinesterase activity was significantly decreased in 300 mu g/L group after thiamethoxam exposure for 96 h. Correspondingly, thiamethoxam exposure with 300 mu g/L for 24 h resulted in significantly downregulated transcriptional levels of synaptic transmission -related genes (e.g. dopamine-, gamma-aminobutyric acid-and serotonin-related receptors). Therefore, thiame-thoxam may be harmful and cause potential toxic threats such as neurotoxicity and metabolic damage to crustaceans.

• 单位
  海南大学