Disruptive ecotoxicological effects of fluoxetine on serotoninergic signaling and enteric neurogenesis in early zebrafish larvae (Danio rerio)

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Environmental toxicology and pharmacology Pub Date : 2025-06-01 Epub Date: 2025-04-10 DOI:10.1016/j.etap.2025.104698
Kainã Rocha Cabrera Fagundes , Natalia Kasica , Małgorzata Potoczna , Shiho Okitsu-Sakurayama , Piotr Podlasz , Renata de Britto Mari
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Abstract

This study investigated the multilevel effects of environmentally relevant concentrations of fluoxetine on serotonergic signaling and enteric neurogenesis in early zebrafish larvae (Danio rerio). To this end, zebrafish were exposed to various concentrations of fluoxetine for four days, from the 1,000-cell stage to 4 days post-fertilization (dpf).Following exposure, whole larvae were subjected to molecular, morphological, and behavioral analyses. All tested concentrations led to upregulation of the serotonin transporter (slc6a4a). At intermediate concentrations, overexpression of the serotonin receptor htr1aa was observed. The highest concentration caused a reduced total enteric neurons density, while the intermediate concentration reduced the density of serotonergic enteric neurons. Additionally, the highest concentration decreased larval locomotion and impaired their ability to differentiate between light and dark phases.Across all tested concentrations, fluoxetine disrupted serotonergic signaling, impaired enteric neurogenesis, and induced sedative-like behavioral effects.
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氟西汀对早期斑马鱼幼鱼血清素信号和肠内神经发生的破坏性生态毒理学影响
本研究研究了环境相关浓度氟西汀对早期斑马鱼幼鱼血清素能信号传导和肠内神经发生的多水平影响。为此,斑马鱼从1000个细胞阶段到受精后4天,暴露于不同浓度的氟西汀四天。暴露后,对整个幼虫进行分子、形态和行为分析。所有测试浓度导致血清素转运体(slc6a4a)上调。在中等浓度下,观察到血清素受体htr1aa过表达。最高浓度使总肠神经元密度降低,而中等浓度使血清素能肠神经元密度降低。此外,高浓度会降低幼虫的运动能力,损害它们区分明暗阶段的能力。在所有测试浓度中,氟西汀破坏了血清素能信号,损害了肠内神经发生,并诱导了类似镇静剂的行为效应。
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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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