Evidence of genotoxicity, neurotoxicity, and antioxidant imbalance in silver catfish Rhamdia quelen after subchronic exposure to diisopentyl phthalate

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation research. Genetic toxicology and environmental mutagenesis Pub Date : 2023-09-28 DOI:10.1016/j.mrgentox.2023.503702
Laís Fernanda Oya-Silva , Izonete Cristina Guiloski , Taynah Vicari , Bruna Deda , Fellip Rodrigues Marcondes , Rafael Dias Simeoni , Maiara Carolina Perussolo , Anderson Joel Martino-Andrade , Daniela Morais Leme , Helena Cristina Silva de Assis , Marta Margarete Cestari
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Abstract

Diisopentyl phthalate (DiPeP) is a plasticizer with significant offer and application in Brazilian industries. This is attributed to its origin, which is closely linked to the refining process of sugarcane for ethanol production in the country. In this work, we developed a model for trophic exposure to environmentally relevant doses (5, 25, and 125 ng/g of DiPeP) to identify possible target tissues and toxic effects promoted by subchronic exposure to DiPeP in a Neotropical catfish species (Rhamdia quelen). After thirty days of exposure, blood, liver, kidney, brain, and muscle were collected and studied regarding DNA damage in blood cells and biochemical analyses. The kidney was the most affected organ, as in the head kidney, genotoxicity was evidenced in all groups exposed to DiPeP. Besides, the caudal kidney showed a reduction in the superoxide dismutase and glutathione peroxidase activities as well as a reduced glutathione concentration. In the liver, exposure to 125 ng/g of DiPeP increased glutathione S-transferase activity and reduced glutathione levels. In muscle, acetylcholinesterase (AChE) was reduced. However, in the brain, an increase in AChE activity was observed after the exposure to lowest doses. In contrast, a significant reduction of brain AChE activity after exposure to the highest dose was detected. The pronounced genotoxicity observed in head kidney cells is of concern, as it may compromise different functions performed by this organ (e.g., hematopoiesis, immune and endocrine functions). In our study, DiPeP proved to be a compound of environmental concern since we have evidenced its nephrotoxic and neurotoxic potential even in low doses.

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亚慢性暴露于邻苯二甲酸二异戊酯后银鲶鱼遗传毒性、神经毒性和抗氧化失衡的证据
邻苯二甲酸二异戊酯(DiPeP)是一种在巴西工业中具有重要应用价值的增塑剂。这归因于它的起源,它与该国用于乙醇生产的甘蔗精炼过程密切相关。在这项工作中,我们开发了一个营养暴露于环境相关剂量(5、25和125纳克/克DiPeP)的模型,以确定新热带鲶鱼(Rhamdia quelen)亚慢性暴露于DiPeP所促进的可能靶组织和毒性作用。暴露30天后,收集血液、肝脏、肾脏、大脑和肌肉,并研究血细胞中的DNA损伤和生化分析。肾脏是受影响最大的器官,因为在头部肾脏中,所有暴露于DiPeP的组都证明了遗传毒性。此外,尾肾的超氧化物歧化酶和谷胱甘肽过氧化物酶活性降低,谷胱甘肽浓度降低。在肝脏中,暴露于125纳克/克的DiPeP可增加谷胱甘肽S-转移酶活性并降低谷胱甘肽水平。在肌肉中,乙酰胆碱酯酶(AChE)减少。然而,在大脑中,在暴露于最低剂量后,观察到AChE活性增加。相反,在暴露于最高剂量后,检测到大脑AChE活性显著降低。在头肾细胞中观察到的明显遗传毒性令人担忧,因为它可能会损害该器官的不同功能(如造血、免疫和内分泌功能)。在我们的研究中,DiPeP被证明是一种环境问题化合物,因为我们已经证明即使在低剂量下也具有肾毒性和神经毒性潜力。
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来源期刊
CiteScore
3.80
自引率
5.30%
发文量
84
审稿时长
105 days
期刊介绍: Mutation Research - Genetic Toxicology and Environmental Mutagenesis (MRGTEM) publishes papers advancing knowledge in the field of genetic toxicology. Papers are welcomed in the following areas: New developments in genotoxicity testing of chemical agents (e.g. improvements in methodology of assay systems and interpretation of results). Alternatives to and refinement of the use of animals in genotoxicity testing. Nano-genotoxicology, the study of genotoxicity hazards and risks related to novel man-made nanomaterials. Studies of epigenetic changes in relation to genotoxic effects. The use of structure-activity relationships in predicting genotoxic effects. The isolation and chemical characterization of novel environmental mutagens. The measurement of genotoxic effects in human populations, when accompanied by quantitative measurements of environmental or occupational exposures. The application of novel technologies for assessing the hazard and risks associated with genotoxic substances (e.g. OMICS or other high-throughput approaches to genotoxicity testing). MRGTEM is now accepting submissions for a new section of the journal: Current Topics in Genotoxicity Testing, that will be dedicated to the discussion of current issues relating to design, interpretation and strategic use of genotoxicity tests. This section is envisaged to include discussions relating to the development of new international testing guidelines, but also to wider topics in the field. The evaluation of contrasting or opposing viewpoints is welcomed as long as the presentation is in accordance with the journal''s aims, scope, and policies.
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