Department of Pharmacology and Toxicology, Faculty of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Students Research Committee, School of Pharmacy, Shahid Beheshti University of Medical SciencesTehran, Iran.
Department of Occupational Therapy, School of Rehabilitation Sciences, Iran University of Medical Sciences, Tehran, Iran; Rehabilitation Research Center, School of Rehabilitation Sciences, Iran University of Medical Sciences, Tehran, Iran.
Neurotoxicology. 2019 Jul;73:40-49. doi: 10.1016/j.neuro.2019.02.014. Epub 2019 Feb 22.
Mephedrone (4-methylmethcathinone) is a new and popular drug of abuse and also widely available on the internet and still legal in some parts of the world. The central nervous system is the target of mephedrone and recent evidence suggested that mephedrone could affect mitochondria in brain tissue. However, the underlying mechanisms of mephedrone toxicity in brain mitochondria have not yet been well understood. In this study, mitochondria from three separate parts of rat brain hippocampus, cortex, and cerebellum were obtained using differential centrifugation and were incubated with different concentrations of mephedrone (3, 6 and 12 μM). Then, the mitochondrial parameters toxicity were determined. The results showed that mephedrone (3, 6 and 12 μM) induced impairment in the activity of the mitochondrial complex II and IV. Also, mephedrone (3, 6 and 12 μM) increased mitochondrial reactive oxygen species (ROS) level, collapsed mitochondria membrane potential (MMP), induced swelling in the mitochondria and damaged the mitochondrial outer membrane (MOM) in the mitochondria obtained from hippocampus, cortex, and cerebellum, which in all cases is associated with the cytochrome c release. Furthermore, increased disturbance in oxidative phosphorylation was also shown by the decrease in ATP level in mephedrone-treated mitochondria indicating mitochondrial dysfunction in separate parts of the brain. This study suggests that mephedrone via increasing oxidative stress and impairment of the mitochondrial respiratory chain in the hippocampus, cortex, and cerebellum may play a key role in the neurotoxicity.
标题:Mephedrone(4-甲基甲卡西酮)对大鼠脑内不同区域线粒体的毒性作用
摘要:4-甲基甲卡西酮(Mephedrone)是一种新型的滥用药物,在互联网上广泛存在,在世界上的一些地方仍被合法使用。Mephedrone 的作用靶点是中枢神经系统,最近的证据表明它可能影响脑组织中的线粒体。然而,Mephedrone 对脑线粒体毒性的潜在机制尚未被充分理解。在这项研究中,我们使用差速离心法从大鼠海马体、大脑皮层和小脑三个不同部位提取线粒体,并与不同浓度的 Mephedrone(3、6 和 12μM)孵育。然后,测定线粒体参数毒性。结果表明,Mephedrone(3、6 和 12μM)可诱导线粒体复合物 II 和 IV 的活性受损。此外,Mephedrone(3、6 和 12μM)还可增加线粒体活性氧(ROS)水平,破坏线粒体膜电位(MMP),诱导线粒体肿胀,并损伤海马体、大脑皮层和小脑的线粒体外膜(MOM),所有这些都与细胞色素 c 的释放有关。此外,Mephedrone 还可通过降低线粒体中 ATP 水平,导致氧化磷酸化的严重紊乱,这表明线粒体功能障碍与脑内不同区域的神经毒性有关。本研究表明,Mephedrone 可能通过增加海马体、大脑皮层和小脑的氧化应激和线粒体呼吸链损伤,在神经毒性中发挥关键作用。