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慢性无机汞暴露后大鼠唾液腺的 DNA 损伤和蛋白质组特征变化。

DNA Damage and Proteomic Profile Changes in Rat Salivary Glands After Chronic Exposure to Inorganic Mercury.

机构信息

Laboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, n. 01, Guamá, Belém, 66075-110, Brazil.

Section of Parasitology, Evandro Chagas Institute, Ananindeua, Brazil.

出版信息

Biol Trace Elem Res. 2022 Sep;200(9):3983-3995. doi: 10.1007/s12011-021-02986-7. Epub 2022 Jan 10.

Abstract

Mercury (Hg) is a toxic metal that became a public health problem due to environmental contamination caused by anthropogenic activity. In this sense, oral homeostasis can undergo changes due to the toxic effects of metal on the salivary glands. Therefore, our objective was to investigate the proteomic and genotoxic changes in salivary glands after exposure to inorganic mercury (IHg). Forty Wistar rats that were divided into a control group, which received distilled water, and an exposed group, which received 0.375 mg/kg of mercury chloride for 45 days via orogastric gavage. After that, the animals were euthanized, and the parotid and submandibular glands were collected for analysis of the genotoxic effects, using the comet assay and proteome global profile assessment. The results showed that IHg promoted damage to cellular DNA associated with proteomic changes that showed events such as oxidative stress, mitochondrial dysfunction, changes in the cytoskeleton, and apoptosis. Therefore, these findings show a profile of molecular changes due to the interactions of IHg with several proteins and mechanisms inherent to the cell, which consequently may result in dysfunction of the salivary glands and impaired homeostasis of the oral cavity.

摘要

汞(Hg)是一种有毒金属,由于人为活动造成的环境污染,已成为公共卫生问题。在这种情况下,由于金属对唾液腺的毒性作用,口腔内环境可能会发生变化。因此,我们的目的是研究无机汞(IHg)暴露后唾液腺的蛋白质组和遗传毒性变化。将 40 只 Wistar 大鼠分为对照组(给予蒸馏水)和实验组(经口灌胃给予 0.375mg/kg 氯化汞,共 45 天)。之后,处死动物,收集腮腺和颌下腺,通过彗星试验和蛋白质组全谱分析评估遗传毒性效应。结果表明,IHg 可引起与蛋白质组变化相关的细胞 DNA 损伤,表明发生了氧化应激、线粒体功能障碍、细胞骨架改变和细胞凋亡等事件。因此,这些发现显示了由于 IHg 与几种蛋白质的相互作用以及细胞固有的多种机制导致的分子变化特征,这可能导致唾液腺功能障碍和口腔内环境稳态受损。

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