Hudson Matthew R, Foreman Joshua, Rind Gil, Manning Elizabeth E, Jones Nigel C, van den Buuse Maarten
Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC 3052, Australia.
Department of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.
Brain Sci. 2022 Nov 5;12(11):1503. doi: 10.3390/brainsci12111503.
Dysregulation of high-frequency neuronal oscillations has been implicated in the pathophysiology of schizophrenia. Chronic methamphetamine (METH) use can induce psychosis similar to paranoid schizophrenia. The current study in mice aimed to determine the effect of chronic METH treatment on ongoing and evoked neuronal oscillations. C57BL/6 mice were treated with METH or vehicle control for three weeks and implanted with extradural recording electrodes. Two weeks after the last METH injection, mice underwent three EEG recording sessions to measure ongoing and auditory-evoked gamma and beta oscillatory power in response to an acute challenge with METH (2 mg/kg), the NMDA receptor antagonist MK-801 (0.3 mg/kg), or saline control. A separate group of mice pretreated with METH showed significantly greater locomotor hyperactivity to an acute METH challenge, confirming long-term sensitisation. Chronic METH did not affect ongoing or evoked gamma or beta power. Acute MK-801 challenge reduced ongoing beta power whereas acute METH challenge significantly increased ongoing gamma power. Both MK-801 and METH challenge suppressed evoked gamma power. Chronic METH treatment did not modulate these acute drug effects. There were minor effects of chronic METH and acute METH and MK-801 on selected components of event-related potential (ERP) waves. In conclusion, chronic METH treatment did not exert neuroplastic effects on the regulation of cortical gamma oscillations in a manner consistent with schizophrenia, despite causing behavioural sensitisation.
高频神经元振荡失调与精神分裂症的病理生理学有关。长期使用甲基苯丙胺(METH)可诱发类似于偏执型精神分裂症的精神病。当前对小鼠的研究旨在确定长期METH治疗对持续和诱发的神经元振荡的影响。将C57BL/6小鼠用METH或载体对照处理三周,并植入硬膜外记录电极。在最后一次METH注射两周后,小鼠进行三次脑电图记录,以测量对METH(2mg/kg)、NMDA受体拮抗剂MK-801(0.3mg/kg)或生理盐水对照的急性挑战的持续和听觉诱发的γ和β振荡功率。另一组预先用METH处理的小鼠对急性METH挑战表现出明显更大的运动性多动,证实了长期致敏。长期METH不影响持续或诱发的γ或β功率。急性MK-801挑战降低了持续的β功率,而急性METH挑战显著增加了持续的γ功率。MK-801和METH挑战均抑制了诱发的γ功率。长期METH治疗并未调节这些急性药物作用。长期METH以及急性METH和MK-801对事件相关电位(ERP)波的选定成分有轻微影响。总之,尽管长期METH治疗会引起行为致敏,但并未以与精神分裂症一致的方式对皮质γ振荡调节产生神经可塑性作用。