Mallamaci Rosanna, Barbarossa Alexia, Carocci Alessia, Meleleo Daniela
Department of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", 70125 Bari, Italy.
Department of Pharmacy-Pharmaceutical Sciences, University of Bari "Aldo Moro", 70125 Bari, Italy.
Foods. 2024 Jan 28;13(3):419. doi: 10.3390/foods13030419.
Ellagic acid (EA), a polyphenolic constituent of plant origin, has been thoroughly investigated for its hypothesised pharmacological properties among which antioxidant and neuroprotective activities are included. The present study was designed to explore whether EA could attenuate heavy metal (cadmium, mercury, and lead)-induced neurotoxicity in SH-SY5Y cells, which were utilized as a model system for brain cells. MTT and LDH assays were performed to examine the viability of the SH-SY5Y cells after exposure to Cd, Hg, and Pb (either individually or in combination with EA) as well as the effects of necrotic cell death, respectively. Furthermore, 2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA), a cell-based assay, was performed to determine whether EA could protect SH-SY5Y from heavy metal-induced oxidative stress. Results allowed us to assess the capability of EA to enhance the number of viable SH-SY5Y cells after exposure to heavy metal toxicity. Pre-treatment with EA showed a considerable, concentration-dependent, cytoprotective effect, particularly against Cd-induced toxicity. This effect was confirmed through the reduction of LDH release after the simultaneous cell treatment with Cd and EA compared with Cd-treated cells. Furthermore, a significant, concentration-dependent decrease in reactive oxygen species (ROS) production, induced by HO or heavy metals, was observed in the same model. Overall, the obtained results provide further insight into the protective role of EA against heavy metal-induced neurotoxicity and oxidative stress, thus indicating the potential beneficial effects of the consumption of EA-rich foods. However, to confirm its effects, well-designed human randomized controlled trials are needed to fill the existing gap between experimental and clinical research.
鞣花酸(EA)是一种植物来源的多酚成分,其假定的药理特性,包括抗氧化和神经保护活性,已得到充分研究。本研究旨在探讨EA是否能减轻重金属(镉、汞和铅)诱导的SH-SY5Y细胞神经毒性,该细胞系用作脑细胞的模型系统。进行MTT和LDH测定,以分别检测SH-SY5Y细胞暴露于镉、汞和铅(单独或与EA联合)后的活力以及坏死性细胞死亡的影响。此外,进行了基于细胞的2',7'-二氯二氢荧光素二乙酸酯(DCFH-DA)测定,以确定EA是否能保护SH-SY5Y细胞免受重金属诱导的氧化应激。结果使我们能够评估EA在暴露于重金属毒性后增加存活SH-SY5Y细胞数量的能力。EA预处理显示出相当大的、浓度依赖性的细胞保护作用,尤其是对镉诱导的毒性。与镉处理的细胞相比,镉和EA同时处理细胞后LDH释放减少,证实了这种作用。此外,在同一模型中观察到,由HO或重金属诱导的活性氧(ROS)产生显著且浓度依赖性降低。总体而言,所得结果进一步深入了解了EA对重金属诱导的神经毒性和氧化应激的保护作用,从而表明食用富含EA的食物可能具有有益效果。然而,为了证实其效果,需要精心设计的人类随机对照试验来填补现有实验研究和临床研究之间的差距。