Bar-Ilan University, Leslie and Susan Gonda Multidisciplinary Brain Research Center, Ramat-Gan 52900, Israel.
J Neurophysiol. 2010 Dec;104(6):3261-75. doi: 10.1152/jn.00093.2010. Epub 2010 Jun 30.
Chorea is a basal-ganglia (BG) related hyperkinetic movement disorder characterized by irregular continuous involuntary movements. Chorea and related hyperbehavioral disorders may be induced in behaving primates by local microinjections of the GABA(A) antagonist bicuculline to the globus pallidus externus (GPe). We performed multielectrode extracellular recordings in the GPe and in the globus pallidus internus (GPi) before, during, and after bicuculline microinjections. Bicuculline led to an increase in the firing rate and a change in the firing pattern of GPe neurons. Two types of abnormal neuronal firing patterns were detected in GPe neurons close to the bicuculline microinjection site: continuous high-frequency activity and bistable activity, in which neurons transitioned between high-frequency and complete cessation of firing. Neuronal activity remained uncorrelated within and between the GPe and the GPi, with no evidence for propagation of the focal GPe abnormal activity downstream to the GPi. Despite reduction in the information capacity of bicuculline-affected GPe neurons, the ability to encode behavioral events was maintained. We found similar responses of GPe neurons to bicuculline in vitro in the rat, suggesting a basic cellular mechanism underlying these abnormal firing patterns. These results demonstrate that chorea is associated with focal neuronal changes that are not complemented by global changes in the BG nuclei. This suggests a mechanism of stochastic phasic alteration of BG control leading to the chaotic nature of chorea. Thus rather than imposing a globalized state of cortical excitability, chorea might be associated with changes in internal information processing within the BG.
舞蹈症是一种基底节(BG)相关的运动障碍,表现为不规则的连续不自主运动。局部微量注射 GABA(A) 拮抗剂荷包牡丹碱到苍白球外(GPe)可以在行为灵长类动物中诱导舞蹈症和相关的多动障碍。我们在微注射前后在 GPe 和苍白球内(GPi)进行了多电极细胞外记录。荷包牡丹碱导致 GPe 神经元的放电率增加和放电模式改变。在靠近荷包牡丹碱微注射部位的 GPe 神经元中检测到两种异常神经元放电模式:连续高频活动和双稳态活动,其中神经元在高频和完全停止放电之间转换。神经元活动在 GPe 内和 GPe 与 GPi 之间仍然没有相关性,没有证据表明焦点 GPe 异常活动向下游 GPi 传播。尽管受荷包牡丹碱影响的 GPe 神经元的信息容量减少,但编码行为事件的能力得以维持。我们在大鼠的体外实验中发现了 GPe 神经元对荷包牡丹碱的类似反应,这表明这些异常放电模式存在基本的细胞机制。这些结果表明,舞蹈症与局部神经元变化有关,而不是与 BG 核的全局变化有关。这表明了一种随机相位改变 BG 控制的机制,导致舞蹈症的混沌性质。因此,舞蹈症可能与 BG 内部信息处理的变化有关,而不是与皮层兴奋性的全局化状态有关。