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迷走神经背核不是帕金森病的必要触发部位:对α-突触核蛋白分期的批判性分析。

The dorsal motor nucleus of the vagus is not an obligatory trigger site of Parkinson's disease: a critical analysis of alpha-synuclein staging.

作者信息

Kalaitzakis M E, Graeber M B, Gentleman S M, Pearce R K B

机构信息

University Department of Neuropathology, Division of Neuroscience and Mental Health, Imperial College London, Hammersmith Hospitals Trust, London, UK.

出版信息

Neuropathol Appl Neurobiol. 2008 Jun;34(3):284-95. doi: 10.1111/j.1365-2990.2007.00923.x. Epub 2007 Dec 5.

Abstract

AIMS

It has been proposed that alpha-synuclein (alpha Syn) pathology in Parkinson's disease (PD) spreads in a predictable caudo-rostral way with the earliest changes seen in the dorsal motor nucleus of the vagus nerve (DMV). However, the reliability of this stereotypical spread of alpha Syn pathology has been questioned. In addition, the comparative occurrence of alpha Syn pathology in the spinal cord and brain has not been closely studied.

METHODS

In order to address these issues, we have examined 71 cases of PD from the UK Parkinson's Disease Society Tissue Bank at Imperial College, London. The incidence and topographic distribution of alpha Syn pathology in several brain regions and the spinal cord were assessed.

RESULTS

The most affected regions were the substantia nigra (SN; in 100% of cases) followed by the Nucleus Basalis of Meynert (NBM) in 98.5%. Fifty-three per cent of cases showed a distribution pattern of alpha Syn compatible with a caudo-rostral spread of alpha Syn through the PD brain. However, 47% of the cases did not fit the predicted spread of alpha Syn pathology and in 7% the DMV was not affected even though alpha Syn inclusions were found in SN and cortical regions. We also observed a high incidence of alpha Syn in the spinal cord with concomitant affection of the DMV and in a few cases in the absence of DMV involvement.

CONCLUSIONS

Our results demonstrate a predominant involvement of the SN and NBM in PD but do not support the existence of a medullary induction site of alpha Syn pathology in all PD brains.

摘要

目的

有人提出帕金森病(PD)中的α-突触核蛋白(αSyn)病理变化以可预测的尾-头方向扩散,最早的变化出现在迷走神经背运动核(DMV)。然而,αSyn病理这种刻板扩散的可靠性受到了质疑。此外,αSyn病理在脊髓和脑内的相对发生率尚未得到深入研究。

方法

为了解决这些问题,我们检查了来自伦敦帝国理工学院英国帕金森病协会组织库的71例PD病例。评估了αSyn病理在几个脑区和脊髓中的发生率及地形分布。

结果

受影响最严重的区域是黑质(SN;100%的病例),其次是Meynert基底核(NBM),占98.5%。53%的病例显示αSyn的分布模式与αSyn通过PD脑的尾-头扩散一致。然而,47%的病例不符合αSyn病理的预测扩散模式,7%的病例中,即使在SN和皮质区域发现了αSyn包涵体,DMV也未受影响。我们还观察到脊髓中αSyn的高发生率,伴有DMV受累,少数情况下无DMV受累。

结论

我们的结果表明SN和NBM在PD中主要受累,但不支持所有PD脑中存在αSyn病理的延髓诱导位点。

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