Peng Jian-Chao, Deng Yue, Song Han-Xiao, Fang Yuan-Yuan, Gan Cui-Liu, Lin Jun-Jie, Luo Jing-Jing, Zheng Xiao-Wei, Aschner Michael, Jiang Yue-Ming
Department of Toxicology, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Guangxi Colleges and Universities Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, Nanning 530021, China.
Brain Sci. 2023 Feb 22;13(3):382. doi: 10.3390/brainsci13030382.
Combined exposure to lead and cadmium is common in occupational environments. However, the effects of co-exposure to Pb-Cd on neurotoxicity have not been fully clarified. Sodium para-aminosalicylic acid (PAS-Na) has previously been shown to protect neurons from Pb-induced toxicity. This study aimed to investigate the beneficial effect of PAS-Na against co-exposure to Pb-Cd-induced neurodegeneration in SH-SY5Y cells.
The MTT assay was used to detect the effects of Pb and Cd alone, or in combination, on SH-SY5Y cell survival. The effects of Pb and Cd alone or in combination on oxidative stress were assessed by reactive oxygen species (ROS) level. Nrf2, the master switch for antioxidant responses, was detected by immunofluorescence. Protein expression levels of PI3K, Akt, p-Akt, Nrf2 and HO-1 were determined by Western blot analysis.
MTT assay results established that the survival rate of SH-SY5Y cells was not significantly affected by exposure to 1 μmol/L lead, 0.25 μmol/L cadmium, and 1-fold Pb-Cd mixture (1 μmol/L Pb + 0.25 μmol/L Cd), while 10-fold Pb-Cd combined exposure (10 μmol/L Pb + 2.5 μmol/L Cd) significantly reduced the survival rate of SH-SY5Y cells. Combined Pb-Cd exposure significantly increased intracellular ROS levels, and N-Acetyl-L-cysteine (NAC) treatment in the 10 μmol/L Pb + 2.5 μmol/L Cd group significantly decreased ROS expression levels, attenuating the levels of oxidative stress. Protein expression of PI3K and p-Akt significantly decreased in the 10 μmol/L Pb + 2.5 μmol/L Cd group, while the expression of PI3K and p-Akt protein increased after PAS-Na intervention. Immunofluorescence analysis showed that levels of Nrf2 in the nucleus increased in the 10 μmol/L Pb + 2.5 μmol/L Cd group, along with Nrf2 protein levels, suggesting that Nrf2 was translocated from the cytoplasm into the nucleus upon combined Pb-Cd exposure. In addition, HO-1 protein expression level, a downstream gene product of Nrf2, was increased. In response to NAC intervention, HO-1 protein expression levels significantly decreased. PAS-Na had the same intervention effect as NAC.
Combined exposure to Pb-Cd induced oxidative stress and cytotoxicity in SH-SY5Y cells. PAS-Na displayed antagonistic effects on neurodegenerative changes induced by combined Pb-Cd exposure; hence, it may afford a novel treatment modality for exposure to these metals.
在职业环境中,铅和镉的联合暴露很常见。然而,铅 - 镉共同暴露对神经毒性的影响尚未完全阐明。对氨基水杨酸钠(PAS-Na)先前已被证明可保护神经元免受铅诱导的毒性。本研究旨在探讨PAS-Na对SH-SY5Y细胞中铅 - 镉联合暴露诱导的神经退行性变的有益作用。
采用MTT法检测单独或联合铅和镉对SH-SY5Y细胞存活的影响。通过活性氧(ROS)水平评估单独或联合铅和镉对氧化应激的影响。通过免疫荧光检测抗氧化反应的主开关Nrf2。通过蛋白质印迹分析测定PI3K、Akt、p-Akt、Nrf2和HO-1的蛋白质表达水平。
MTT分析结果表明,暴露于1μmol/L铅、0.25μmol/L镉和1倍铅 - 镉混合物(1μmol/L铅 + 0.25μmol/L镉)对SH-SY5Y细胞的存活率没有显著影响,而10倍铅 - 镉联合暴露(10μmol/L铅 + 2.5μmol/L镉)显著降低了SH-SY5Y细胞的存活率。铅 - 镉联合暴露显著增加细胞内ROS水平,10μmol/L铅 + 2.5μmol/L镉组中N-乙酰-L-半胱氨酸(NAC)处理显著降低ROS表达水平,减轻氧化应激水平。10μmol/L铅 + 2.5μmol/L镉组中PI3K和p-Akt的蛋白质表达显著降低,而PAS-Na干预后PI3K和p-Akt蛋白质表达增加。免疫荧光分析显示,10μmol/L铅 + 2.5μmol/L镉组中细胞核内Nrf2水平增加,同时Nrf2蛋白质水平也增加,表明铅 - 镉联合暴露时Nrf2从细胞质转移到细胞核。此外,Nrf2的下游基因产物HO-1蛋白质表达水平增加。对NAC干预的反应中,HO-1蛋白质表达水平显著降低。PAS-Na具有与NAC相同的干预效果。
铅 - 镉联合暴露在SH-SY5Y细胞中诱导氧化应激和细胞毒性。PAS-Na对铅 - 镉联合暴露诱导的神经退行性变化具有拮抗作用;因此,它可能为这些金属的暴露提供一种新的治疗方式。