Schneider J, Olry C
Rev Electroencephalogr Neurophysiol Clin. 1982 Dec;12(4):291-8. doi: 10.1016/s0370-4475(82)80015-4.
Based on the spectral analysis of drug-induced beta activity in 15 normal subjects, the authors distinguish 2 groups of beta spectra: (1) Peaked beta spectra with stable frequency (25 +/- 0.3 Hz) and an essentially precentral localization. Such spectra must depend on the activation of a dense and circumscribed population of neurons having strong synchronizing power. (2) Beta spectra widely dispersed with regard to frequency and topography, having generators that are more widely distributed or with a lesser power of synchronization. The spectra show significant interhemispheric energy asymmetries which are accentuated by eye opening. Finally, these two types of beta activity, although exhibiting a preferentially precentral localization, are not altered by movements. In contrast they react, while maintaining energy to eye opening by energetic changes, which allows one to distinguish these activities from sensorimotor rhythms.
基于对15名正常受试者药物诱发的β活动的频谱分析,作者区分出两组β频谱:(1)频率稳定(25±0.3赫兹)且主要位于中央前回的尖峰β频谱。这种频谱必定依赖于具有强大同步能力的密集且局限的神经元群体的激活。(2)在频率和地形图上广泛分散的β频谱,其发生器分布更广泛或同步能力较弱。这些频谱显示出明显的半球间能量不对称,睁眼会使其加剧。最后,这两种类型的β活动虽然主要位于中央前回,但不受运动影响。相反,它们会通过能量变化对睁眼做出反应,同时保持能量,这使得人们能够将这些活动与感觉运动节律区分开来。