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

机译:长期暴露于SSRI西酞普兰会诱导斑马鱼的神经毒性作用

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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 μg/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 μg/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 μg/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.
机译:残留抗抑郁药在世界范围内越来越受到关注,但缺乏关于其对非靶标水生动物的长期神经毒性影响的关键信息。本研究以选择性5-羟色胺再摄取抑制剂西酞普兰(0.1-100 μg/L)为研究对象,研究其对斑马鱼2代运动功能、学习和记忆的长期影响,并探讨其对F1幼虫的影响可逆性。与F0~+幼虫不同,我们发现F1~+幼虫在连续暴露于100 μg/L的西酞普兰时感觉运动性能下降,F1~-幼虫转移至清洁培养基后未发现不良反应。全贴片免疫荧光实验表明,运动障碍与脊髓运动神经元(MNs)的轴突投射有关。对于F0~+成年人,长期西酞普兰暴露主要引起男性特异性的运动、学习和记忆能力下降。对5-羟色胺能和胆碱能MNs的分析显示,雄性斑马鱼脊髓没有显着变化。相反,谷氨酸能脊髓膜肾病的数量减少,可能与运动功能受损有关。此外,100 μg/L西酞普兰治疗可显著减少多巴胺能神经元数量,但未观察到成人端脑中明显的神经元凋亡。总体而言,本研究为长期暴露于西酞普兰的神经毒性机制提供了神经行为证据和新的见解,并可能有助于评估含西酞普兰的抗抑郁药物带来的环境和健康风险。

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