I-Med. UL, Department of Toxicology and Food Sciences, Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.
Biol Trace Elem Res. 2013 Apr;152(1):113-6. doi: 10.1007/s12011-012-9597-0. Epub 2013 Jan 15.
Manganese (Mn) is an essential metal for biological systems; however, occupational or clinical exposure to high levels of Mn can produce a neurological disorder called manganism. Oxidative stress and neuroinflammation play major roles in the Mn-induced neurodegeneration leading to dysfunction of the basal ganglia. We investigated the toxic effects of MnCl2 in an immortalized rat brain endothelial cell line (RBE4) and the protective effects of the radical scavenging aminosalicylic acids, 5-aminosalicylic acid (5-ASA) and 4-aminosalicylic acid (4-PAS). Mn cytotoxicity was determined with 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) reduction and lactate dehydrogenase (LDH) activity. A significant decrease in MTT reduction concomitant with increased LDH release was noted in RBE4 cells exposed for 24 h to MnCl2 (600 and 800 μM; p < 0.0001). Our results establish that compared to 4-PAS, 5-ASA has greater efficacy in protecting RBE4 cells from Mn-induced neurotoxicity after preexposure to MnCl2 800 μM (p < 0.0001).
锰(Mn)是生物系统必需的金属;然而,职业性或临床性暴露于高水平的 Mn 会导致一种叫做锰中毒的神经疾病。氧化应激和神经炎症在 Mn 诱导的神经退行性变中起主要作用,导致基底神经节功能障碍。我们研究了 MnCl2 在永生化大鼠脑内皮细胞系(RBE4)中的毒性作用,以及自由基清除剂氨基水杨酸的保护作用,5-氨基水杨酸(5-ASA)和 4-氨基水杨酸(4-PAS)。通过 3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴化物(MTT)还原和乳酸脱氢酶(LDH)活性来确定 Mn 细胞毒性。在暴露于 MnCl2(600 和 800 μM;p < 0.0001)24 小时的 RBE4 细胞中,MTT 还原显著减少,同时 LDH 释放增加。与 4-PAS 相比,我们的结果表明,5-ASA 在预暴露于 800 μM MnCl2 后对 RBE4 细胞具有更大的保护作用,可防止 Mn 诱导的神经毒性(p < 0.0001)。