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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >High-frequency stimulation of the subthalamic nucleus silences subthalamic neurons: a possible cellular mechanism in Parkinson's disease.
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High-frequency stimulation of the subthalamic nucleus silences subthalamic neurons: a possible cellular mechanism in Parkinson's disease.

机译:丘脑底核的高频刺激使丘脑底神经元沉默:帕金森氏病的一种可能的细胞机制。

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The subthalamic nucleus participates in the control of movement and is considered a surgical target in the treatment of parkinsonian symptoms. Using the rat brain in vitro slice technique we show that sustained high-frequency (>100 Hz) electrical stimulation (i.e., 'tetanic stimulation') of the nucleus, as used in humans to treat Parkinson's disease, silenced subthalamic neurons. Two main cell types were identified. 'Tonic cells' (68%) showed delayed inward rectification, fired continuously, switched to bursting and stopped firing when strongly depolarized with injected current. Tetanic stimulation of the nucleus induced a steady depolarization ( approximately 18 mV) that triggered action potentials at a high rate followed by bursts and finally ( approximately 25 s) totally silenced tonic cells. The control tonic activity was recovered rapidly (<10 s) after ending stimulation. 'Phasic cells' (25%) discharged a single initial brief burst of action potentials both when depolarized by prolonged current injection and tetanic stimulation and did not show inward rectification. An infrequent cell type called 'phasic-tonic' (7%) showed a mixed discharge. We suggest that the silencing effect of tetanic stimulation is not a frequency-dependent presynaptic depression and could result from the gradual inactivation of Na(+)-mediated action potentials. These findings suggest that the remission of parkinsonian symptoms by treatment with high-frequency electrical stimulation of the subthalamic nucleus in humans may primarily reside on its capacity to suppress the action potential activity of subthalamic neurons.
机译:丘脑下核参与运动的控制并且被认为是治疗帕金森氏症状的外科手术目标。使用大鼠脑体外切片技术,我们显示了对核的持续高频(> 100 Hz)电刺激(即``破伤风刺激''),用于治疗帕金森氏病的人类使丘脑下神经元沉默。确定了两种主要细胞类型。 “ Tonic细胞”(68%)显示出延迟的向内整流,连续发射,在注入电流强烈去极化后切换为爆发并停止发射。对核的强直刺激会导致稳定的去极化(约18 mV),从而以高速率触发动作电位,随后爆发,最后(约25 s)完全沉默的滋补细胞。刺激结束后,对照的补品活性迅速恢复(<10 s)。当通过长时间的电流注入和强直性刺激去极化时,“相细胞”(25%)释放出单个初始的短暂的动作电位爆发,并且没有表现出内向整流。一种罕见的细胞类型称为“相张性”(7%),表现出混合放电。我们建议强直性刺激的沉默效应不是频率依赖的突触前抑郁症,可能是由Na(+)介导的动作电位逐渐失活引起的。这些发现表明,通过高频电刺激人丘脑底核的治疗,帕金森病症状的缓解可能主要取决于其抑制丘脑底神经元动作电位活性的能力。

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