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Effects of New Psychoactive Substance Esketamine on Behaviors and Transcription of Genes in Dopamine and GABA Pathways in Zebrafish Larvae.

Si-Ying Li, Wen-Jun Shi, Dong-Dong Ma, Jin-Ge Zhang, Zhi-Jie Lu, Xiao-Bing Long, Xin Liu, Chu-Shu Huang, Guang-Guo Ying

Bulletin of environmental contamination and toxicology March 31, 2024 DOI: 10.1007/s00128-024-03883-0 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Zebrafish larvae
Intervention Esketamine
Dose 12.4 ng L⁻¹ to 11141.1 ng L⁻¹
Duration 7 days post fertilization
Topics Esketamine
Keywords Neurotoxicity Transcription Zebrafish Psychopharmacology Behavioral toxicology Drug safety Molecular biology
Citations 9
Key findings Esketamine at 12.4 ng L⁻¹ reduces touch response and swimming behavior in zebrafish larvae and increases transcription of genes in dopamine and GABA pathways, indicating neurotoxicity.

Abstract

Esketamine (ESK) is the S-enantiomer of ketamine racemate (a new psychoactive substance) that can result in illusions, and alter hearing, vision, and proprioception in human and mouse. Up to now, the neurotoxicity caused by ESK at environmental level in fish is still unclear. This work studied the effects of ESK on behaviors and transcriptions of genes in dopamine and GABA pathways in zebrafish larvae at ranging from 12.4 ng L- 1 to 11141.1 ng L- 1 for 7 days post fertilization (dpf). The results showed that ESK at 12.4 ng L- 1 significantly reduced the touch response of the larvae at 48 hpf. ESK at 12.4 ng L- 1 also reduced the time and distance of larvae swimming at the outer zone during light period, which implied that ESK might potentially decrease the anxiety level of larvae. In addition, ESK increased the transcription of th, ddc, drd1a, drd3 and drd4a in dopamine pathway. Similarly, ESK raised the transcription of slc6a1b, slc6a13 and slc12a2 in GABA pathway. This study suggested that ESK could affect the heart rate and behaviors accompanying with transcriptional alterations of genes in DA and GABA pathways at early-staged zebrafish, which resulted in neurotoxicity in zebrafish larvae.

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