Laboratorio de Toxicología Ambiental, Facultad de Química, Universidad Autónoma del Estado de México, Paseo Colón intersección Paseo Tollocan, Colonia Residencial Colón, CP 50120 Toluca, Estado de México, Mexico.
Laboratorio de Toxicología Ambiental, Facultad de Química, Universidad Autónoma del Estado de México, Paseo Colón intersección Paseo Tollocan, Colonia Residencial Colón, CP 50120 Toluca, Estado de México, Mexico.
Sci Total Environ. 2022 May 1;819:153095. doi: 10.1016/j.scitotenv.2022.153095. Epub 2022 Jan 14.
Recent studies have shown guanylurea (GUA) alters the growth and development of fish, induces oxidative stress, and disrupts the levels and expression of several genes, metabolites, and proteins related to the overall fitness of fish. Nonetheless, up to date, no study has assessed the potential neurotoxic effects that GUA may induce in non-target organisms. To fill the current knowledge gaps about the effects of this metabolite in the central nervous system of fish, we aimed to determine whether or not environmentally relevant concentrations of this metabolite may disrupt the behavior, redox status, AChE activity in Danio rerio adults. In addition, we also meant to assess if 25, 50, and 200 μg/L of GUA can alter the expression of several antioxidant defenses-, apoptosis-, AMPK pathway-, and neuronal communication-related genes in the brain of fish exposed for four months to GUA. Our results demonstrated that chronic exposure to GUA altered the swimming behavior of D. rerio, as fish remained more time frozen and traveled less distance in the tank compared to the control group. Moreover, this metabolite significantly increased the levels of oxidative damage biomarkers and inhibited the activity of acetylcholinesterase of fish in a concentration-dependent manner. Concerning gene expression, environmentally relevant concentrations of GUA downregulated the expression GRID2IP, PCDH17, and PCDH19, but upregulated Nrf1, Nrf2, p53, BAX, CASP3, PRKAA1, PRKAA2, and APP in fish after four months of exposure. Collectively, we can conclude that GUA may alter the homeostasis of several essential brain biomarkers, generating anxiety-like behavior in fish.
最近的研究表明,胍(GUA)会改变鱼类的生长和发育,诱导氧化应激,并破坏与鱼类整体健康相关的几种基因、代谢物和蛋白质的水平和表达。尽管如此,迄今为止,尚无研究评估 GUA 可能对非目标生物产生的潜在神经毒性作用。为了填补关于这种代谢物在鱼类中枢神经系统中的作用的现有知识空白,我们旨在确定环境相关浓度的这种代谢物是否会破坏成年斑马鱼的行为、氧化还原状态和乙酰胆碱酯酶活性。此外,我们还旨在评估 25、50 和 200μg/L 的 GUA 是否会改变暴露于 GUA 四个月的鱼脑中几种与抗氧化防御、细胞凋亡、AMPK 途径和神经元通讯相关的基因的表达。我们的结果表明,慢性暴露于 GUA 改变了斑马鱼的游泳行为,与对照组相比,鱼在水箱中停留的时间更长,游动的距离更短。此外,这种代谢物以浓度依赖的方式显著增加了氧化损伤生物标志物的水平,并抑制了鱼类乙酰胆碱酯酶的活性。关于基因表达,环境相关浓度的 GUA 下调了 GRID2IP、PCDH17 和 PCDH19 的表达,但在暴露四个月后上调了 Nrf1、Nrf2、p53、BAX、CASP3、PRKAA1、PRKAA2 和 APP 的表达。总的来说,我们可以得出结论,GUA 可能会改变几种重要脑生物标志物的体内平衡,在鱼类中产生类似焦虑的行为。