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苍白球神经元活动:对肌张力障碍模型的启示

Pallidal neuronal activity: implications for models of dystonia.

作者信息

Hutchison William D, Lang Anthony E, Dostrovsky Jonathan O, Lozano Andres M

机构信息

Department of Surgery, Division of Neurosurgery and Toronto Western Research Institute, Toronto Western Hospital and Faculty of Medicine, University of Toronto, Ontario, Canada.

出版信息

Ann Neurol. 2003 Apr;53(4):480-8. doi: 10.1002/ana.10474.

Abstract

Dystonia is a neurological syndrome involving sustained contractions of opposing muscles leading to abnormal movements and postures. Recent studies report abnormally low pallidal neuronal activity in patients with generalized dystonia, suggesting hyperkinetic disorders result from underactive basal ganglia output. We examined this hypothesis in 11 patients with segmental and generalized dystonia undergoing microelectrode exploration of the internal globus pallidus (GPi) before pallidotomy or deep brain stimulation (DBS) implantation. The mean firing rates and firing patterns were compared with those in six patients with Parkinson's disease (PD). In seven patients who underwent surgery under local anesthesia, the mean GPi firing rate was 77 Hz, similar to the 74 Hz observed in the PD patients. However, in three dystonic patients under propofol anesthesia, GPi mean firing rate was much reduced (31 Hz), and the firing pattern was distinguished by long pauses in activity, as reported by others. Low-dose propofol in one other dystonia patient also seemed to suppress GPi firing. These results indicate that an abnormally low basal ganglia output is not the sine qua non of dystonia. The widely accepted pathophysiological models of dystonia that propose global decreases in basal ganglia output need to be viewed with caution in light of these findings.

摘要

肌张力障碍是一种神经综合征,涉及拮抗肌的持续收缩,导致异常运动和姿势。最近的研究报告称,全身性肌张力障碍患者苍白球神经元活动异常低下,提示运动亢进性疾病是由基底神经节输出活动不足所致。我们对11例节段性和全身性肌张力障碍患者进行了研究,这些患者在接受苍白球切开术或脑深部电刺激(DBS)植入术前,接受了内侧苍白球(GPi)的微电极探查。将平均放电率和放电模式与6例帕金森病(PD)患者进行了比较。在7例接受局部麻醉手术的患者中,GPi平均放电率为77Hz,与PD患者中观察到的74Hz相似。然而,在3例接受丙泊酚麻醉的肌张力障碍患者中,GPi平均放电率大幅降低(31Hz),且放电模式的特点是活动出现长时间停顿,正如其他人所报告的那样。另一例肌张力障碍患者使用低剂量丙泊酚似乎也抑制了GPi放电。这些结果表明,基底神经节输出异常低下并非肌张力障碍的必要条件。鉴于这些发现,对于广泛接受的提出基底神经节输出整体降低的肌张力障碍病理生理模型,需要谨慎看待。

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