Lysergic Acid Diethylamide Alters the Effects of Brain Stimulation in Rodents

Lucas Dwiel, Angela Henricks, Elise Bragg, Jeff Nicol, Jiang Gui, Wilder Doucette
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Abstract

Background: Psychedelic drugs have resurged in neuroscience and psychiatry with promising success in psychedelic-assisted therapy for the treatment of anxiety, depression, and addiction. At the cellular level, psychedelic drugs elicit neuroplastic processes 24 h after administration, priming neural circuits for change. The acute effects of psychedelic drugs are well characterized with functional imaging and neural oscillations showing an increase in the entropy of spontaneous cortical activity. Hypotheses: We hypothesized that cortical–striatal oscillations recorded in rats would confirm the effects of psychedelic drugs. We also hypothesized that brain stimulation delivered 24 h after lysergic acid diethylamide (LSD) administration would lead to different effects than brain stimulation alone. Methods: We recorded local field potential oscillations from rats after LSD or saline (SAL) administration and determined whether exposure to these treatments altered the effect of a targeted intervention (brain stimulation) 24 h later. Results: We confirmed acutely decreased low frequency power across the brain when rats are given LSD. We also demonstrated these altered states return to baseline after 24 h. Brain stimulation applied in the previously reported window of heightened neuroplasticity produced distinct shifts in brain state compared with brain stimulation applied 24 h after SAL administration. Conclusions: Despite the acute effects of LSD disappearing after 24 h, there are still latent effects that interact with brain stimulation to create larger and distinct changes in brain activity compared with brain stimulation alone. Our proof-of-concept findings are the first to suggest that psychedelic drugs could work in combination with brain stimulation to achieve enhanced effects on brain activity and future study will assess impacts on stimulation-induced changes in behavior.
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麦角酸二乙胺改变啮齿动物脑刺激的效果
背景:迷幻药在神经科学和精神病学中重新兴起,在治疗焦虑、抑郁和成瘾的迷幻辅助疗法中取得了有希望的成功。在细胞水平上,迷幻药物在给药24小时后引发神经可塑性过程,引发神经回路的变化。迷幻药物的急性作用表现为功能成像和神经振荡,显示自发皮层活动熵的增加。假设:我们假设在大鼠中记录的皮质纹状体振荡可以证实迷幻药物的作用。我们还假设在给予麦角酸二乙胺(LSD) 24小时后给予脑刺激会导致与单独脑刺激不同的效果。方法:我们记录了LSD或生理盐水(SAL)给药后大鼠的局部场电位振荡,并确定暴露于这些治疗是否会改变24小时后靶向干预(脑刺激)的效果。结果:我们证实给大鼠服用LSD后,整个大脑的低频功率急剧下降。我们还证明,这些改变的状态在24小时后恢复到基线。与SAL给药后24小时进行脑刺激相比,在先前报道的神经可塑性增强窗口进行脑刺激产生了明显的脑状态变化。结论:尽管LSD的急性效应在24 h后消失,但与单独的脑刺激相比,仍存在与脑刺激相互作用的潜在效应,使脑活动发生更大、更明显的变化。我们的概念验证研究结果首次表明,迷幻药物可以与大脑刺激结合使用,以增强对大脑活动的影响,未来的研究将评估刺激引起的行为改变的影响。
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