Division of Neurotoxicology; FDA/NCTR, Jefferson, AR, USA.
Curr Neuropharmacol. 2011 Mar;9(1):236-9. doi: 10.2174/157015911795017209.
Advances in computer technology have allowed quantification of the electroencephalogram (EEG) and expansion of quantitative EEG (qEEG) analysis in neurophysiology, as well as clinical neurology, with great success. Among the variety of techniques in this field, frequency (spectral) analysis using Fast Fourier Transforms (FFT) provides a sensitive tool for time-course studies of different compounds acting on particular neurotransmitter systems. Studies presented here include Electrocorticogram (ECoG) analysis following exposure to a glutamic acid analogue - domoic acid (DOM), psychoactive indole alkaloid - ibogaine, as well as cocaine and gamma-hydroxybutyrate (GHB). The ECoG was recorded in conscious rats via a tether and swivel system. The EEG signal frequency analysis revealed an association between slow-wave EEG activity delta and theta and the type of behavioral seizures following DOM administration. Analyses of power spectra obtained in rats exposed to cocaine alone or after pretreatment with ibogaine indicated the contribution of the serotonergic system in ibogaine mediated response to cocaine (increased power in alpha(1) band). Ibogaine also lowered the threshold for cocaine-induced electrographic seizures (increased power in the low-frequency bands, delta and theta). Daily intraperitoneal administration of cocaine for two weeks was associated with a reduction in slow-wave ECoG activity 24 hrs following the last injection when compared with controls. Similar decreased cortical activity in low-frequency bands observed in chronic cocaine users has been associated with reduced metabolic activity in the frontal cortex. The FFT analyses of power spectra relative to baseline indicated a significant energy increase over all except beta(2) frequency bands following exposure to 400 and 800 mg/kg GHB. The EEG alterations detected in rats following exposure to GHB resemble absence seizures observed in human petit mal epilepsy. Spectral analysis of the EEG signals combined with behavioral observations may prove to be a useful approach in studying chronic exposure to drugs of abuse and treatment of drug dependence.
计算机技术的进步使得对脑电图(EEG)进行量化以及对神经生理学和临床神经病学中的定量脑电图(qEEG)分析得以扩展,取得了巨大成功。在该领域的各种技术中,使用快速傅里叶变换(FFT)的频率(谱)分析为研究不同化合物对特定神经递质系统的作用提供了敏感的工具。这里介绍的研究包括在暴露于谷氨酸类似物- 海人酸(DOM)、精神活性吲哚生物碱-伊博加因以及可卡因和 γ-羟基丁酸(GHB)后,对皮质脑电图(ECoG)进行分析。通过系绳和旋转系统在清醒大鼠中记录 ECoG。EEG 信号频率分析显示,在给予 DOM 后,慢波 EEG 活动 δ 和θ与行为性癫痫发作的类型之间存在关联。对单独暴露于可卡因或用伊博加因预处理后暴露于可卡因的大鼠获得的功率谱进行分析表明,5-羟色胺系统在伊博加因介导的可卡因反应中起作用(α1 频段的功率增加)。伊博加因还降低了可卡因引起的脑电图癫痫发作的阈值(低频带、δ 和θ的功率增加)。与对照组相比,连续两周每天腹腔注射可卡因后,最后一次注射 24 小时后 ECoG 慢波活动减少。在慢性可卡因使用者中观察到的低频带皮质活动减少与额叶皮层代谢活动减少有关。与基线相比,FFT 分析相对功率谱表明,在暴露于 400 和 800mg/kg GHB 后,除β2 频段外,所有频段的能量均显著增加。大鼠暴露于 GHB 后检测到的 EEG 改变类似于人类小发作性癫痫中的失神发作。EEG 信号的频谱分析结合行为观察可能成为研究慢性滥用药物和药物依赖治疗的有用方法。