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精神分裂症中的纤维通路病理学、突触丧失和皮质功能下降。

Fiber pathway pathology, synapse loss and decline of cortical function in schizophrenia.

机构信息

The Brain and Mind Research Institute, University of Sydney, Sydney, NSW, Australia.

出版信息

PLoS One. 2013 Apr 8;8(4):e60518. doi: 10.1371/journal.pone.0060518. Print 2013.

Abstract

A quantitative cortical model is developed, based on both computational and simulation approaches, which relates measured changes in cortical activity of gray matter with changes in the integrity of longitudinal fiber pathways. The model consists of modules of up to 5,000 neurons each, 80% excitatory and 20% inhibitory, with these having different degrees of synaptic connectiveness both within a module as well as between modules. It is shown that if the inter-modular synaptic connections are reduced to zero while maintaining the intra-modular synaptic connections constant, then activity in the modules is reduced by about 50%. This agrees with experimental observations in which cortical electrical activity in a region of interest, measured using the rate of oxidative glucose metabolism (CMRglc(ox)), is reduced by about 50% when the cortical region is isolated, either by surgical means or by transient cold block. There is also a 50% decrease in measured cortical activity following inactivation of the nucleus of Meynert and the intra-laminar nuclei of the thalamus, which arise either following appropriate lesions or in sleep. This occurs in the model if the inter-modular synaptic connections require input from these nuclei in order to function. In schizophrenia there is a 24% decrease in functional anisotropy of longitudinal fasciculi accompanied by a 7% decrease in cortical activity (CMRglc(ox)).The cortical model predicts this, namely for a 24% decrease in the functioning of the inter-modular connections, either through the complete loss of 24% of axons subserving the connections or due to such a decrease in the efficacy of all the inter-modular connections, there will be about a 7% decrease in the activity of the modules. This work suggests that deterioration of longitudinal fasciculi in schizophrenia explains the loss of activity in the gray matter.

摘要

建立了一个基于计算和模拟方法的皮质定量模型,该模型将皮质灰度活动的测量变化与纵向纤维通路完整性的变化联系起来。该模型由多达 5000 个神经元组成的模块组成,其中 80%是兴奋性的,20%是抑制性的,这些神经元在模块内和模块之间具有不同程度的突触连接性。结果表明,如果将模块间的突触连接减少到零,同时保持模块内的突触连接不变,那么模块中的活动将减少约 50%。这与实验观察结果一致,即通过手术或短暂冷阻断将感兴趣区域的皮质电活动(CMRglc(ox))测量到的皮质区域隔离时,皮质区域的皮质电活动会减少约 50%;当适当的病变或睡眠导致 Meynert 核和丘脑层间核失活时,也会出现皮质活动减少 50%的情况。如果模块间的突触连接需要这些核的输入才能发挥作用,则模型中会出现这种情况。在精神分裂症中,纵向束的功能各向异性降低 24%,同时皮质活动(CMRglc(ox))降低 7%。皮质模型预测了这一点,即如果模块间连接的功能降低 24%,无论是由于连接的轴突完全丧失 24%,还是由于所有模块间连接的效率降低,模块的活动都会降低约 7%。这项工作表明,精神分裂症中纵向束的恶化解释了灰质活动的丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917b/3620229/ebff5bc50dd8/pone.0060518.g001.jpg

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