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帕金森病和进行性核上性麻痹中的丘脑底核

The subthalamic nucleus in Parkinson's disease and progressive supranuclear palsy.

作者信息

Hardman C D, Halliday G M, McRitchie D A, Morris J G

机构信息

Prince of Wales Medical Research Institute, Prince of Wales Hospital, Randwick, NSW, Australia.

出版信息

J Neuropathol Exp Neurol. 1997 Feb;56(2):132-42. doi: 10.1097/00005072-199702000-00003.

Abstract

The subthalamus has become a promising target for the neurosurgical treatment of parkinsonian symptoms. We have used unbiased counting techniques to quantify the neuronal populations of the subthalamic nucleus in patients with idiopathic Parkinson's disease and progressive supranuclear palsy. In addition, the type of calcium binding proteins contained within these subthalamic neurons was established using immunohistochemistry. Most of the 550,000 subthalamic neurons contain either parvalbumin or calretinin calcium binding proteins, and patients with idiopathic Parkinson's disease sustained no damage to this nucleus. This is consistent with current theories of basal ganglia circuitry, which postulate that overstimulation of this excitatory nucleus contributes to the inhibition of the motor thalamus via the activation of inhibitory relays. In contrast, we found that there was substantial cell loss in the subthalamus in progressive supranuclear palsy (45 to 85% neuronal reduction) and that both cell types were equally affected. Extracellular neurofibrillary tangles as well as tau-positive glia were observed in the subthalamus of these cases. As the patients with Parkinson's disease and progressive supranuclear palsy all had overlapping parkinsonian symptoms, the loss of subthalamic stimulation within the basal ganglia of progressive supranuclear palsy cases is puzzling, unless their parkinsonian symptoms were generated by an alternate mechanism.

摘要

丘脑底核已成为帕金森氏症症状神经外科治疗的一个有前景的靶点。我们运用无偏差计数技术对特发性帕金森病和进行性核上性麻痹患者的丘脑底核神经元数量进行了量化。此外,通过免疫组织化学确定了这些丘脑底核神经元中所含钙结合蛋白的类型。55万个丘脑底核神经元中的大多数含有小白蛋白或钙视网膜蛋白钙结合蛋白,特发性帕金森病患者的该核未受损伤。这与基底神经节回路的当前理论一致,该理论假定这个兴奋性核的过度刺激通过抑制性中继的激活导致运动丘脑的抑制。相比之下,我们发现进行性核上性麻痹患者的丘脑底核有大量细胞丢失(神经元减少45%至85%),且两种细胞类型受影响程度相同。在这些病例的丘脑底核中观察到细胞外神经原纤维缠结以及tau阳性胶质细胞。由于帕金森病和进行性核上性麻痹患者都有重叠的帕金森氏症症状,进行性核上性麻痹病例基底神经节内丘脑底核刺激的丧失令人费解,除非他们的帕金森氏症症状是由另一种机制产生的。

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