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神经功能未受损的老年受试者脊髓和外周自主神经系统的α-突触核蛋白病理学

Alpha-synuclein pathology of the spinal and peripheral autonomic nervous system in neurologically unimpaired elderly subjects.

作者信息

Bloch A, Probst A, Bissig H, Adams H, Tolnay M

机构信息

Institute of Pathology, Department of Neuropathology, University Hospital Basel, Basel, Switzerland.

出版信息

Neuropathol Appl Neurobiol. 2006 Jun;32(3):284-95. doi: 10.1111/j.1365-2990.2006.00727.x.

Abstract

Studies on cases with incidental Lewy body disease (ILBD) suggest that alpha-synuclein (alphaSN) pathology of Parkinson's disease (PD) starts in lower brainstem nuclei and in the olfactory bulb. However, medullary structures as the induction site of alphaSN pathology have been questioned as large parts of the nervous system, including the spinal cord and the peripheral autonomic nervous system (PANS), have not been examined in ILBD. Thus, the time course of PD lesions in the spinal cord or PANS in relation to medullary lesions remains unknown. We collected 98 post mortem cases with no reference to PD-associated symptoms on clinical records. alphaSN pathology was found in the central nervous system, including the spinal cord, and in the PANS in 17 (17.3%) cases. alphaSN pathology was encountered in autonomic nuclei of the thoracic spinal cord, brainstem and olfactory nerves in 17/17, in sacral parasympathetic nuclei in 15/16, in the myenteric plexus of oesophagus in 14/17, in sympathetic ganglia in 14/17, and in the vagus nerve in 12/16 cases. In addition to the thoracic lateral horns, a high number of alphaSN lesions was also found in non-autonomic spinal cord nuclei. Considering supraspinal structures our cases corresponded roughly to the recently described sequential order of alphaSN involvement in PD. Our study indicates, however, that the autonomic nuclei of the spinal cord and the PANS belong to the most constantly and earliest affected regions next to medullary structures and the olfactory nerves. A larger cohort of ILBD cases will be needed to pinpoint the precise induction site of alphaSN pathology among these structures.

摘要

对伴发路易体病(ILBD)病例的研究表明,帕金森病(PD)的α-突触核蛋白(αSN)病理改变始于脑桥下部核团和嗅球。然而,由于在ILBD研究中未对包括脊髓和外周自主神经系统(PANS)在内的大部分神经系统进行检查,因此作为αSN病理改变诱导部位的延髓结构受到了质疑。因此,脊髓或PANS中PD病变相对于延髓病变的时间进程仍不清楚。我们收集了98例尸检病例,临床记录中未提及与PD相关的症状。在17例(17.3%)病例的中枢神经系统(包括脊髓)和PANS中发现了αSN病理改变。在17/17例的胸段脊髓自主神经核、脑干和嗅神经中,15/16例的骶副交感神经核中,14/17例的食管肌间神经丛中,14/17例的交感神经节中,以及12/16例的迷走神经中发现了αSN病理改变。除胸外侧角外,在非自主脊髓核中也发现了大量αSN病变。考虑到脊髓以上结构,我们的病例大致符合最近描述的PD中αSN受累的顺序。然而,我们的研究表明,脊髓自主神经核和PANS是继延髓结构和嗅神经之后最常且最早受影响的区域。需要更大规模的ILBD病例队列来确定这些结构中αSN病理改变的确切诱导部位。

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