Faria Melissa, Prats Eva, Bellot Marina, Gomez-Canela Cristian, Raldúa Demetrio
Institute for Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, 08034 Barcelona, Spain.
Research and Development Centre (CID-CSIC), Jordi Girona 18, 08034 Barcelona, Spain.
Toxics. 2021 May 25;9(6):118. doi: 10.3390/toxics9060118.
This study examines the effects of acute pharmacological modulation of the serotonergic system over zebrafish larvae's cognitive, basic, and defense locomotor behaviors, using a medium to high throughput screening assay. Furthermore, the relationship between behavior, enzyme activity related to neurotransmitter metabolism, neurotransmitter levels, and gene expression was also determined. Modulation of larvae serotonergic system was accomplished by 24 h exposure to single and opposite pharmacodynamics co-exposure to three model psychopharmaceuticals with antagonistic and agonistic serotonin signaling properties: 2.5 mM 4-Chloro-DL-phenylalanine (PCPA) and 5 µM deprenyl and 0.5 µM fluoxetine, respectively. Similar behavioral outcome was observed for deprenyl and fluoxetine, which was reflected as hypolocomotion, decrease in larvae defensive responses, and cognitive impairment. Contrarily, PCPA induced hyperlocomotion and increase in larvae escape response. Deprenyl exposure effects were more pronounced at a lower level of organization than fluoxetine, with complete inhibition of monoamine oxidase (MAO) activity, dramatic increase of 5-HT and dopamine (DA) levels, and downregulation of serotonin synthesis and transporter genes. PCPA showed mainly effects over serotonin and dopamine's main degradation metabolites. Finally, co-exposure between agonistic and antagonist serotonin signaling drugs reviled full recovery of zebrafish impaired locomotor and defense responses, 5-HT synthesis gene expression, and partial recovery of 5-HT levels. The findings of this study suggest that zebrafish larvae can be highly sensitive and a useful vertebrate model for short-term exposure to serotonin signaling changes.
本研究采用中高通量筛选试验,研究了血清素能系统的急性药理学调节对斑马鱼幼体认知、基本和防御性运动行为的影响。此外,还确定了行为、与神经递质代谢相关的酶活性、神经递质水平和基因表达之间的关系。通过将幼体暴露于具有拮抗和激动血清素信号特性的三种模型精神药物的单一和相反药效学共同暴露24小时,来实现对血清素能系统的调节:分别为2.5 mM 4-氯-DL-苯丙氨酸(PCPA)、5 µM司来吉兰和0.5 µM氟西汀。司来吉兰和氟西汀观察到类似的行为结果,表现为运动减少、幼体防御反应降低和认知障碍。相反,PCPA诱导运动亢进和幼体逃避反应增加。司来吉兰暴露的影响在较低组织水平上比氟西汀更明显,表现为单胺氧化酶(MAO)活性完全抑制、5-羟色胺(5-HT)和多巴胺(DA)水平显著增加以及血清素合成和转运基因下调。PCPA主要对血清素和多巴胺的主要降解代谢产物有影响。最后,激动剂和拮抗剂血清素信号药物之间的共同暴露揭示了斑马鱼受损的运动和防御反应、5-HT合成基因表达的完全恢复以及5-HT水平的部分恢复。本研究结果表明,斑马鱼幼体对血清素信号变化的短期暴露可能高度敏感,是一种有用的脊椎动物模型。