镁-伊博格碱治疗对创伤性脑损伤退伍军人皮质振荡和神经复杂性的影响

IF 8.7
Jennifer I. Lissemore, Anna Chaiken, Kirsten N. Cherian, Derrick Buchanan, Flint Espil, Jackob N. Keynan, Malvika Sridhar, Camarin E. Rolle, Manish Saggar, Corey J. Keller, Nolan R. Williams
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摘要

创伤性脑损伤可导致慢性精神和认知症状,并伴有皮层振荡性质和神经复杂性的改变。最近发现用镁-伊博格碱治疗可以改善创伤性脑损伤的后遗症,但伊博格碱对人类皮层振荡和复杂性的影响尚不清楚。在一项开放标签的观察性研究中,对30名退伍军人进行了镁-伊博格碱治疗前、治疗后3.5天和治疗后1个月的静息状态脑电图。我们评估了伊博格碱对皮质振荡和复杂性的影响,以及这些神经生理效应与伊博格碱治疗的精神和认知结果的关系。治疗后,较慢振荡(θ - α)的功率增加,而较高频率(β - γ)的功率下降。相应地,θ / β比值在治疗后增加,这与认知抑制的改善相关。治疗后α峰频率和神经复杂性降低,并持续到1个月的随访。这些神经生理指标与伊博加因后执行功能改善、创伤后应激障碍和焦虑相关。总之,这些发现表明,镁-伊博格碱治疗后,大脑活动的时空复杂性降低,休息时大脑皮层振荡“减慢”,这可能与伊博格碱治疗后精神和认知的改善有关,从而为伊博格碱对人类大脑功能的影响提供了关键的见解。需要后续对照临床试验来证实这一初始单臂试验的发现。在创伤性脑损伤的退伍军人中,镁-伊博格碱单次治疗可以增强皮层θ波和α波的强度,降低β波和α波的强度,降低神经的复杂性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Magnesium–ibogaine therapy effects on cortical oscillations and neural complexity in veterans with traumatic brain injury

Magnesium–ibogaine therapy effects on cortical oscillations and neural complexity in veterans with traumatic brain injury
Traumatic brain injury can lead to chronic psychiatric and cognitive symptoms, coupled with changes to the nature of cortical oscillations and neural complexity. Treatment with magnesium–ibogaine was recently found to improve the sequelae of traumatic brain injury, yet the effects of ibogaine on human cortical oscillations and complexity are unknown. Resting-state electroencephalography was performed prospectively before, 3.5 days after and 1 month after magnesium–ibogaine therapy in an observational, open-label study of 30 combat veterans. We assessed the effects of ibogaine on cortical oscillations and complexity and how these neurophysiological effects relate to psychiatric and cognitive outcomes of ibogaine treatment. After treatment, slower oscillations (theta–alpha) increased in power, and power at higher frequencies (beta–gamma) decreased. Accordingly, the theta/beta ratio increased post-treatment, which correlated with improved cognitive inhibition. Peak alpha frequency and neural complexity were lower after treatment, which persisted at 1-month follow-up. These neurophysiological markers correlated with improved executive function, post-traumatic stress disorder and anxiety after ibogaine. Altogether, these findings suggest reduced spatiotemporal complexity of brain activity and ‘slowing’ of cortical oscillations in the brain at rest after magnesium–ibogaine therapy, which may relate to psychiatric and cognitive improvements after ibogaine, thus providing key insight into the effects of ibogaine on brain function in humans. Follow-up controlled clinical trials are needed to confirm the findings from this initial single-arm trial. A single treatment with magnesium–ibogaine results in enhanced power of cortical theta and alpha oscillations, reduced beta and gamma power and reduced neural complexity in veterans with traumatic brain injury.
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