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神经退行性疾病中的突触易损性。

Synaptic vulnerability in neurodegenerative disease.

作者信息

Wishart Thomas M, Parson Simon H, Gillingwater Thomas H

机构信息

Centre for Integrative Physiology & Centre for Neuroscience Research, University of Edinburgh Medical School, UK.

出版信息

J Neuropathol Exp Neurol. 2006 Aug;65(8):733-9. doi: 10.1097/01.jnen.0000228202.35163.c4.

Abstract

Recent developments in our understanding of the pathophysiological mechanisms underlying degeneration in both the central and peripheral nervous systems have highlighted the critical role that synapses play in the instigation and progression of neuronal loss. In fact, several lines of evidence suggest that previous attempts to delay the onset and progression of clinical symptoms in a broad range of neurodegenerative diseases may have been unsuccessful as a result of a failure to protect synaptic compartments. As a result, the synapse needs to be viewed as an important target for the development of novel protective treatments aimed at preventing or slowing disease progression. We summarize important findings from human studies and animal models demonstrating common synaptic vulnerability across several neurodegenerative diseases. We also discuss recent developments in our understanding of degenerative mechanisms that are known to be localized to synapses and suggest potential ways to harness this understanding to develop synaptoprotective strategies for neurodegenerative disease.

摘要

我们对中枢神经系统和周围神经系统变性潜在病理生理机制的理解,近期取得了一些进展,这些进展突出了突触在神经元丧失的引发和进展中所起的关键作用。事实上,有几条证据表明,先前在多种神经退行性疾病中延迟临床症状发作和进展的尝试可能并不成功,原因是未能保护突触结构。因此,突触应被视为开发旨在预防或减缓疾病进展的新型保护性治疗方法的重要靶点。我们总结了人体研究和动物模型的重要发现,这些发现表明几种神经退行性疾病存在共同的突触易损性。我们还讨论了目前对已知定位于突触的变性机制的理解进展,并提出了利用这一理解来制定神经退行性疾病突触保护策略的潜在方法。

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