Compte Albert, Reig Ramon, Descalzo Vanessa F, Harvey Michael A, Puccini Gabriel D, Sanchez-Vives Maria V
Institut d'Investigacions Biomèdiques August Pi i Sunyer, 08036 Barcelona, Spain.
J Neurosci. 2008 Dec 17;28(51):13828-44. doi: 10.1523/JNEUROSCI.2684-08.2008.
High-frequency oscillations in cortical networks have been linked to a variety of cognitive and perceptual processes. They have also been recorded in small cortical slices in vitro, indicating that neuronal synchronization at these frequencies is generated in the local cortical circuit. However, in vitro experiments have hitherto necessitated exogenous pharmacological or electrical stimulation to generate robust synchronized activity in the beta/gamma range. Here, we demonstrate that the isolated cortical microcircuitry generates beta and gamma oscillations spontaneously in the absence of externally applied neuromodulators or synaptic agonists. We show this in a spontaneously active slice preparation that engages in slow oscillatory activity similar to activity during slow-wave sleep. beta and gamma synchronization appeared during the up states of the slow oscillation. Simultaneous intracellular and extracellular recordings revealed synchronization between the timing of incoming synaptic events and population activity. This rhythm was mechanistically similar to pharmacologically induced gamma rhythms, as it also included sparse, irregular firing of neurons within the population oscillation, predominant involvement of inhibitory neurons, and a decrease of oscillation frequency after barbiturate application. Finally, we show in a computer model how a synaptic loop between excitatory and inhibitory neurons can explain the emergence of both the slow (<1 Hz) and the beta-range oscillations in the neocortical network. We therefore conclude that oscillations in the beta/gamma range that share mechanisms with activity reported in vivo or in pharmacologically activated in vitro preparations can be generated during slow oscillatory activity in the local cortical circuit, even without exogenous pharmacological or electrical stimulation.
皮层网络中的高频振荡与多种认知和感知过程相关联。它们也已在体外的小皮层切片中被记录到,这表明这些频率下的神经元同步是在局部皮层回路中产生的。然而,迄今为止,体外实验需要外源药理学或电刺激才能在β/γ范围内产生强大的同步活动。在此,我们证明,在没有外部施加神经调节剂或突触激动剂的情况下,分离的皮层微电路会自发产生β和γ振荡。我们在一种自发活动的切片标本中展示了这一点,该标本呈现出类似于慢波睡眠期间活动的慢振荡活动。β和γ同步出现在慢振荡的上升期。同时进行的细胞内和细胞外记录揭示了传入突触事件的时间与群体活动之间的同步。这种节律在机制上类似于药理学诱导的γ节律,因为它也包括群体振荡内神经元的稀疏、不规则放电、抑制性神经元的主要参与以及巴比妥酸盐应用后振荡频率的降低。最后,我们在计算机模型中展示了兴奋性和抑制性神经元之间的突触回路如何解释新皮层网络中慢(<1 Hz)振荡和β范围振荡的出现。因此,我们得出结论,即使没有外源药理学或电刺激,在局部皮层回路的慢振荡活动期间,也可以产生与体内报道的活动或药理学激活的体外标本中具有相同机制的β/γ范围内的振荡。