4.8 Article

Long-Term Exposure to SSRI Citalopram Induces Neurotoxic Effects in Zebrafish

期刊

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c01514

关键词

antidepressant; behavior; motor neuron; learning and memory; toxicology

资金

  1. National Key Research and Development Project of China [2019YFC1803402]
  2. National Natural Science Foundation of China [21976202, 42107291]
  3. China Postdoctoral Science Foundation [2021M703405]

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This study investigated the long-term neurotoxic effects of residual antidepressant citalopram on zebrafish. The results showed that continuous exposure to citalopram led to decreased motor function, learning, and memory in both larval and adult zebrafish. However, the effects were reversible in larval zebrafish after transferring to a clean medium. The study provides insights into the neurotoxic mechanisms of citalopram and its potential environmental and health risks.
Residual antidepressants are of increasing concern worldwide, yet critical information on their long-term neurotoxic impacts on nontarget aquatic animals is lacking. Here, we investigated the long-term effects (from 0 to 150 days postfertilization) of the selective serotonin reuptake inhibitor citalopram (0.1-100 mu g/L) on motor function, learning, and memory in zebrafish over two generations and explored the reversibility of the effect in F1 larvae. Unlike F0(+) larvae, we found that F1(+) larvae displayed decreased sensorimotor performance when continuously exposed to citalopram at 100 mu g/L. No adverse effects were found in F1(-) larvae after they were transferred to a clean medium. Whole-mount immunofluorescence assays suggested that the motor impairments were related to axonal projections of the spinal motor neurons (MNs). For F0(+) adults, long-term citalopram exposure mainly caused male-specific declines in motor, learning, and memory performance. Analysis of serotonergic and cholinergic MNs revealed no significant changes in the male zebrafish spinal cord. In contrast, the number of glutamatergic spinal MNs decreased, likely associated with the impairment of motor function. Additionally, treatment with 100 mu g/L citalopram significantly reduced the number of dopaminergic neurons, but no significant neuronal apoptosis was observed in the adult telencephalon. Overall, this study provides neurobehavioral evidence and novel insights into the neurotoxic mechanisms of long-term citalopram exposure and may facilitate the assessment of the environmental and health risks posed by citalopram-containing antidepressant drugs.

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