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慢性暴露于现实浓度的二甲双胍会在成年斑马鱼中引发神经毒性反应。

Chronic exposure to realistic concentrations of metformin prompts a neurotoxic response in Danio rerio adults.

机构信息

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.

出版信息

Sci Total Environ. 2022 Nov 25;849:157888. doi: 10.1016/j.scitotenv.2022.157888. Epub 2022 Aug 9.

Abstract

Metformin (MET) is among the most consumed drugs around the world, and thus, it is considered the uppermost drug in mass discharged into water settings. Nonetheless, data about the deleterious consequences of MET on water organisms are still scarce and require further investigation. Herein, we aimed to establish whether or not chronic exposure to MET (1, 20, and 40 μg/L) may alter the swimming behavior and induce neurotoxicity in Danio rerio adults. After 4 months of exposure, MET-exposed fish exhibited less swimming activity when compared to control fish. Moreover, compared with the control group, MET significantly inhibited the activity of AChE and induced oxidative damage in the brain of fish. Concerning gene expression, MET significantly upregulated the expression of Nrf1, Nrf2, BAX, p53, BACE1, APP, PSEN1, and downregulated CASP3 and CASP9. Although MET did not overexpress the CASP3 gene, we saw a meaningful rise in the activity of this enzyme in the blood of fish exposed to MET compared to the control group, which we then confirmed by a high number of apoptotic cells in the TUNEL assay. Our findings demonstrate that chronic exposure to MET may impair fish swimming behavior, making them more vulnerable to predators.

摘要

二甲双胍(MET)是全球使用最广泛的药物之一,因此被认为是大量排入水系统的首要药物。然而,关于 MET 对水生物的有害影响的数据仍然很少,需要进一步研究。在此,我们旨在确定慢性暴露于 MET(1、20 和 40 μg/L)是否会改变斑马鱼成鱼的游泳行为并引起神经毒性。经过 4 个月的暴露,与对照组相比,MET 暴露的鱼的游泳活动减少。此外,与对照组相比,MET 显著抑制了鱼脑中乙酰胆碱酯酶的活性,并诱导了氧化损伤。关于基因表达,MET 显著上调了 Nrf1、Nrf2、BAX、p53、BACE1、APP、PSEN1 的表达,同时下调了 CASP3 和 CASP9 的表达。尽管 MET 没有过度表达 CASP3 基因,但我们发现与对照组相比,暴露于 MET 的鱼血液中的这种酶的活性显著升高,通过 TUNEL 检测到大量凋亡细胞进一步证实了这一点。我们的研究结果表明,慢性暴露于 MET 可能会损害鱼类的游泳行为,使它们更容易受到捕食者的攻击。

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