Bittencourt Leonardo Oliveira, Chemelo Victória Santos, Aragão Walessa Alana Bragança, Puty Bruna, Dionizio Aline, Teixeira Francisco Bruno, Fernandes Mileni Silva, Silva Márcia Cristina Freitas, Fernandes Luanna Melo Pereira, de Oliveira Edivaldo Herculano Corrêa, Buzalaf Marilia Afonso Rabelo, Crespo-Lopez Maria Elena, Maia Cristiane do Socorro Ferraz, Lima Rafael Rodrigues
Laboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, PA, Brazil.
Department of Biological Sciences, Bauru Dental School, University of São Paulo, Bauru 17012-901, SP, Brazil.
Int J Mol Sci. 2021 Dec 22;23(1):111. doi: 10.3390/ijms23010111.
Mercury is a severe environmental pollutant with neurotoxic effects, especially when exposed for long periods. Although there are several evidences regarding mercury toxicity, little is known about inorganic mercury (IHg) species and cerebellum, one of the main targets of mercury associated with the neurological symptomatology of mercurial poisoning. Besides that, the global proteomic profile assessment is a valuable tool to screen possible biomarkers and elucidate molecular targets of mercury neurotoxicity; however, the literature is still scarce. Thus, this study aimed to investigate the effects of long-term exposure to IHg in adult rats' cerebellum and explore the modulation of the cerebellar proteome associated with biochemical and functional outcomes, providing evidence, in a translational perspective, of new mercury toxicity targets and possible biomarkers. Fifty-four adult rats were exposed to 0.375 mg/kg of HgCl or distilled water for 45 days using intragastric gavage. Then, the motor functions were evaluated by rotarod and inclined plane. The cerebellum was collected to quantify mercury levels, to assess the antioxidant activity against peroxyl radicals (ACAPs), the lipid peroxidation (LPO), the proteomic profile, the cell death nature by cytotoxicity and apoptosis, and the Purkinje cells density. The IHg exposure increased mercury levels in the cerebellum, reducing ACAP and increasing LPO. The proteomic approach revealed a total 419 proteins with different statuses of regulation, associated with different biological processes, such as synaptic signaling, energy metabolism and nervous system development, e.g., all these molecular changes are associated with increased cytotoxicity and apoptosis, with a neurodegenerative pattern on Purkinje cells layer and poor motor coordination and balance. In conclusion, all these findings feature a neurodegenerative process triggered by IHg in the cerebellum that culminated into motor functions deficits, which are associated with several molecular features and may be related to the clinical outcomes of people exposed to the toxicant.
汞是一种具有神经毒性作用的严重环境污染物,长期接触时尤其如此。尽管有若干关于汞毒性的证据,但对于无机汞(IHg)种类与小脑(汞中毒神经症状学相关的主要靶器官之一)之间的关系却知之甚少。除此之外,全球蛋白质组图谱评估是筛选可能的生物标志物和阐明汞神经毒性分子靶点的有价值工具;然而,相关文献仍然匮乏。因此,本研究旨在调查成年大鼠长期暴露于无机汞对小脑的影响,并探索与生化和功能结果相关的小脑蛋白质组的调节情况,从转化医学角度为新的汞毒性靶点和可能的生物标志物提供证据。54只成年大鼠通过灌胃法暴露于0.375mg/kg的氯化汞或蒸馏水中45天。然后,通过转棒试验和斜面试验评估运动功能。采集小脑以量化汞含量、评估针对过氧自由基的抗氧化活性(ACAPs)、脂质过氧化(LPO)、蛋白质组图谱、细胞毒性和凋亡导致的细胞死亡性质以及浦肯野细胞密度。无机汞暴露增加了小脑中的汞含量,降低了ACAP并增加了LPO。蛋白质组学方法揭示了总共419种具有不同调控状态的蛋白质,这些蛋白质与不同的生物学过程相关,如突触信号传导、能量代谢和神经系统发育等,例如,所有这些分子变化都与细胞毒性和凋亡增加相关,在浦肯野细胞层呈现神经退行性模式,且运动协调和平衡能力较差。总之,所有这些发现表明,无机汞在小脑中引发了一个神经退行性过程,最终导致运动功能缺陷,这与若干分子特征相关,并且可能与接触该毒物的人群的临床结果有关。