Department of Histology, Medical University of Gdańsk, 1 Dębinki St, 80-211, Gdańsk, Poland.
Laboratory of Cell Biology, Department of Medical Biotechnology, Intercollegiate Faculty of Biotechnology UG-MUG, Medical University of Gdańsk, Gdańsk, Poland.
Neurotox Res. 2018 Oct;34(3):388-400. doi: 10.1007/s12640-018-9898-y. Epub 2018 Apr 14.
Synthetic cathinones are psychoactive substances, derivatives of a natural psychostimulant cathinone. Although many synthetic cathinones have lost their legal status in many countries, their abuse still continues worldwide. Recently, they have been reported to exert neurotoxic effects in vitro and in vivo. The molecular mechanisms of their action have not been fully elucidated. Recently, they have been linked to the induction of oxidative stress, autophagy, and apoptosis. The aim of this study was to investigate whether 3-fluoromethcathinone (3-FMC), a synthetic cathinone, is able to induce oxidative stress, autophagy, and apoptosis in HT22 immortalized mouse hippocampal cells. We found that treatment of HT22 cells with this compound results in a concentration-dependent increase in the intracellular production of reactive oxygen species. Moreover, 3-FMC induced concentration-dependent conversion of cytosolic LC3-I to membrane-bound LC3-II and formation of autophagic vacuoles. Additionally, the level of p62/SQSTM1 protein decreased after 3-FMC treatment, suggesting that accumulation of autophagic vacuoles resulted from activation rather than inhibition of autophagy. Our results also showed that 3-FMC at millimolar concentration is able to induce caspase-dependent apoptotic cell death in HT22 cells. Our findings suggest that abuse of 3-FMC may disturb neuronal homeostasis and impair functioning of the central nervous system.
合成卡西酮是一种精神活性物质,是天然兴奋剂卡西酮的衍生物。尽管许多合成卡西酮在许多国家已失去合法地位,但它们的滥用仍在全球范围内持续。最近,它们被报道在体外和体内具有神经毒性作用。其作用的分子机制尚未完全阐明。最近,它们与诱导氧化应激、自噬和细胞凋亡有关。本研究旨在探讨合成卡西酮 3-氟甲卡西酮(3-FMC)是否能够诱导 HT22 永生化小鼠海马细胞发生氧化应激、自噬和细胞凋亡。我们发现,该化合物处理 HT22 细胞会导致细胞内活性氧的产生呈浓度依赖性增加。此外,3-FMC 诱导细胞质 LC3-I 向膜结合 LC3-II 的浓度依赖性转化,并形成自噬小泡。此外,3-FMC 处理后 p62/SQSTM1 蛋白水平降低,表明自噬小泡的积累是由于自噬的激活而不是抑制所致。我们的结果还表明,3-FMC 在毫摩尔浓度下能够诱导 HT22 细胞中 caspase 依赖性凋亡细胞死亡。我们的研究结果表明,滥用 3-FMC 可能会扰乱神经元内稳态并损害中枢神经系统的功能。