Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André, SP, Brazil.
Programa de Pós-Graduação em Bioquímica e Bioprospecção (PPGBBIO), Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Instituto de Biologia, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brazil.
Neurotox Res. 2019 Oct;36(3):491-502. doi: 10.1007/s12640-019-00091-1. Epub 2019 Jul 29.
Methylglyoxal (MG) is a dicarbonyl molecule exhibiting high reactivity and is a major responsible for glycation in human cells. Accumulation of MG is seen in certain diseases, including metabolic disturbances and neurodegeneration. Among other effects, MG promotes mitochondrial dysfunction, leading to bioenergetic decline and redox impairment in virtually any nucleated human cells. The detoxification of MG is dependent on the availability of reduced glutathione (GSH), a major antioxidant that is also utilized in phase II detoxification reactions. The synthesis of GSH is mainly controlled by the transcription factor nuclear factor (erythroid-derived 2)-like 2 (Nrf2). The activation of Nrf2 is stimulated by several reactive compounds, including natural molecules produced by plants. Tanshinone I (T-I) is obtained from Salvia miltiorrhiza Bunge and exerts potent cytoprotective actions in different cell types. Thus, we have investigated here whether and how T-I would be able to protect mitochondria of the human neuroblastoma SH-SY5Y cell line exposed to MG. The cells were pretreated with T-I at 2.5 μM for 2 h before the challenge with MG at 500 μM. T-I significantly attenuated the MG-induced loss of cell viability, bioenergetic decline, and redox impairment in SH-SY5Y cells. The inhibition of the GSH synthesis by buthionine sulfoximine (BSO) at 100 μM suppressed the mitochondrial protection promoted by T-I. The silencing of Nrf2 by small interfering RNA (siRNA) abrogated the synthesis of GSH and the mitochondrial protection stimulated by T-I in SH-SY5Y cells. Therefore, T-I induced mitochondrial protection by a mechanism involving the Nrf2/GSH axis in MG-challenged SH-SY5Y cells.
甲基乙二醛 (MG) 是一种具有高反应性的二羰基分子,是导致人体细胞糖基化的主要物质。MG 的积累可见于某些疾病中,包括代谢紊乱和神经退行性疾病。除其他作用外,MG 会促进线粒体功能障碍,导致几乎所有有核人类细胞的生物能量下降和氧化还原损伤。MG 的解毒依赖于还原型谷胱甘肽 (GSH) 的可用性,GSH 是一种主要的抗氧化剂,也用于 II 相解毒反应。GSH 的合成主要受转录因子核因子 (红细胞衍生 2)-样 2 (Nrf2) 的控制。Nrf2 的激活受几种反应性化合物的刺激,包括植物产生的天然分子。丹参酮 I (T-I) 从丹参中提取,在不同类型的细胞中具有强大的细胞保护作用。因此,我们在这里研究了 T-I 是否以及如何能够保护暴露于 MG 的人神经母细胞瘤 SH-SY5Y 细胞系的线粒体。细胞在用 500 μM MG 孵育前,用 2.5 μM 的 T-I 预处理 2 小时。T-I 显著减轻了 MG 诱导的 SH-SY5Y 细胞活力丧失、生物能量下降和氧化还原损伤。用 100 μM 丁硫氨酸亚砜 (BSO) 抑制 GSH 的合成抑制了 T-I 促进的线粒体保护。用小干扰 RNA (siRNA) 沉默 Nrf2 可消除 T-I 刺激的 GSH 合成和线粒体保护。因此,T-I 通过涉及 Nrf2/GSH 轴的机制在 MG 挑战的 SH-SY5Y 细胞中诱导线粒体保护。