4.3 Article

Acute and chronic synaptic pathology in multiple sclerosis gray matter

期刊

MULTIPLE SCLEROSIS JOURNAL
卷 28, 期 3, 页码 369-382

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/13524585211022174

关键词

Multiple sclerosis; synapse; gray matter; glutamate; demyelination; progressive

资金

  1. Cassa di Risparmio di Torino (CRT) [2377.2016]
  2. Department of Excellence grant of the Italian Ministry of Education, University and Research

向作者/读者索取更多资源

The study reveals significant synaptic loss in active demyelinating GM lesions in MS brain tissue, while synaptic density is only mildly reduced in chronic inactive lesions. Additionally, diffuse synaptic loss is observed in MS NLGM compared to control GM.
Objectives: To investigate the extent of synaptic loss, and the contribution of gray matter (GM) inflammation and demyelination to synaptic loss, in multiple sclerosis (MS) brain tissue. Methods: This study was performed on two different post-mortem series of MS and control brains, including deep GM and cortical GM. MS brain samples had been specifically selected for the presence of active demyelinating GM lesions. Over 1,000,000 individual synapses were identified and counted using confocal microscopy, and further characterized as glutamatergic/GABAergic. Synaptic counts were also correlated with neuronal/axonal loss. Results: Important synaptic loss was observed in active demyelinating GM lesions (-58.9%), while in chronic inactive GM lesions, synaptic density was only mildly reduced compared to adjacent non-lesional gray matter (NLGM) (-12.6%). Synaptic loss equally affected glutamatergic and GABAergic synapses. Diffuse synaptic loss was observed in MS NLGM compared to control GM (-21.2% overall). Conclusion: This study provides evidence, in MS brain tissue, of acute synaptic damage/loss during active GM inflammatory demyelination and of synaptic reorganization in chronically demyelinated GM, affecting equally glutamatergic and GABAergic synapses. Furthermore, this study provides a strong indication of widespread synaptic loss in MS NLGM also independently from focal GM demyelination.

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