Grotell Milo, den Hollander Bjørnar, Jalkanen Aaro, Törrönen Essi, Ihalainen Jouni, de Miguel Elena, Dudek Mateusz, Kettunen Mikko I, Hyytiä Petri, Forsberg Markus M, Kankuri Esko, Korpi Esa R
Department of Pharmacology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
School of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland.
Front Pharmacol. 2021 Apr 28;12:679759. doi: 10.3389/fphar.2021.679759. eCollection 2021.
Mephedrone (4-MMC), despite its illegal status, is still a widely used psychoactive substance. Its effects closely mimic those of the classical stimulant drug methamphetamine (METH). Recent research suggests that unlike METH, 4-MMC is not neurotoxic on its own. However, the neurotoxic effects of 4-MMC may be precipitated under certain circumstances, such as administration at high ambient temperatures. Common use of 4-MMC in conjunction with alcohol raises the question whether this co-consumption could also precipitate neurotoxicity. A total of six groups of adolescent rats were treated twice daily for four consecutive days with vehicle, METH (5 mg/kg) or 4-MMC (30 mg/kg), with or without ethanol (1.5 g/kg). To investigate persistent delayed effects of the administrations at two weeks after the final treatments, manganese-enhanced magnetic resonance imaging brain scans were performed. Following the scans, brains were collected for Golgi staining and spine analysis. 4-MMC alone had only subtle effects on neuronal activity. When administered with ethanol, it produced a widespread pattern of deactivation, similar to what was seen with METH-treated rats. These effects were most profound in brain regions which are known to have high dopamine and serotonin activities including hippocampus, nucleus accumbens and caudate-putamen. In the regions showing the strongest activation changes, no morphological changes were observed in spine analysis. By itself 4-MMC showed few long-term effects. However, when co-administered with ethanol, the apparent functional adaptations were profound and comparable to those of neurotoxic METH.
甲氧麻黄酮(4-甲基甲卡西酮)尽管处于非法地位,但仍是一种广泛使用的精神活性物质。其效果与经典兴奋剂甲基苯丙胺(冰毒)极为相似。最近的研究表明,与冰毒不同,4-甲基甲卡西酮本身并无神经毒性。然而,4-甲基甲卡西酮的神经毒性可能在某些情况下诱发,比如在高温环境下给药。4-甲基甲卡西酮与酒精共同使用的情况很常见,这就引发了一个问题,即这种共同使用是否也会诱发神经毒性。总共六组青春期大鼠连续四天每天接受两次处理,分别给予赋形剂、冰毒(5毫克/千克)或4-甲基甲卡西酮(30毫克/千克),同时给予或不给予乙醇(1.5克/千克)。为了研究末次处理两周后给药的持续延迟效应,进行了锰增强磁共振成像脑部扫描。扫描后,收集大脑进行高尔基染色和脊柱分析。单独使用4-甲基甲卡西酮对神经元活动只有细微影响。与乙醇一起给药时,它会产生广泛的失活模式,类似于冰毒处理的大鼠。这些效应在已知具有高多巴胺和5-羟色胺活性的脑区最为显著,包括海马体、伏隔核和尾状核-壳核。在显示出最强激活变化的区域,脊柱分析未观察到形态学变化。4-甲基甲卡西酮本身几乎没有长期影响。然而,与乙醇共同给药时,明显的功能适应性变化很大,与神经毒性冰毒相当。