多类型耦合模型中丘脑前馈和反馈抑制的传播效应

IF 1.6 4区 医学 Q4 NEUROSCIENCES Neuroreport Pub Date : 2024-12-11 Epub Date: 2024-11-06 DOI:10.1097/WNR.0000000000002111
Quanjun Wu, Ranran Li, Yufan Liu, Suyuan Huang, Yuan Chai
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引用次数: 0

摘要

癫痫发作波可以在丘脑皮层耦合模型中传播,这通常发生在功能失常的神经元网络中。然而,丘脑前馈抑制(FFI)和反馈抑制(FBI)作为该网络中两个最重要的微电路,是否具有传播效应仍不清楚。在本研究中,我们首先研究了锥体神经元群-丘脑网状核和特定中继核-丘脑网状核通路在泰勒癫痫发作控制模型中分别作为 FFI 和 FBI 的重要性。随后,我们以FBI为关键参数,构建了2室和3室耦合模型,并通过改变耦合强度评估了它们对其他腔室癫痫发作传播的影响。最后,我们在 10 室模型中重复了上述研究,以确保研究结果的稳健性。通过分析 FFI 和 FBI 的综合效应,我们证实了 FBI 更为有效,而且随着耦合强度的增加,病理状态也确实会发生改变。这些发现阐明了这两种途径在癫痫发作传播过程中的作用,并可能为癫痫的临床治疗提供新的视角。
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Propagation effect of the thalamic feed-forward and feed-back inhibition in multi-type coupling models.

Seizure waves of epilepsy can propagate in a coupled thalamocortical model, which typically occurs in malfunctioning neuronal networks. However, it remains unclear whether thalamic feed-forward inhibition (FFI) and feed-back inhibition (FBI), the two most important microcircuits in this network, have propagation effects. In this study, we first investigated the importance of the pyramidal neuronal population-thalamic reticular nucleus and specific relay nucleus-thalamic reticular nucleus pathways in the Taylor model for seizure control as FFI and FBI, respectively. Subsequently, using the FBI as a crucial parameter, we constructed 2- and 3-compartment coupling models and evaluated their impact on seizure propagation in other chambers by varying the degree of coupling strength. Finally, we replicated the above study in a 10-compartment model to ensure the robustness of the findings. We confirmed that FBI is more effective by analyzing the combined effect of FFI and FBI, and the pathology state does advance as the coupling strength is increased. These findings elucidate the roles that these two pathways play in the propagation of epileptic seizures and may offer fresh perspectives on the clinical management of epilepsy.

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来源期刊
Neuroreport
Neuroreport 医学-神经科学
CiteScore
3.20
自引率
0.00%
发文量
150
审稿时长
1 months
期刊介绍: NeuroReport is a channel for rapid communication of new findings in neuroscience. It is a forum for the publication of short but complete reports of important studies that require very fast publication. Papers are accepted on the basis of the novelty of their finding, on their significance for neuroscience and on a clear need for rapid publication. Preliminary communications are not suitable for the Journal. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool. The core interest of the Journal is on studies that cast light on how the brain (and the whole of the nervous system) works. We aim to give authors a decision on their submission within 2-5 weeks, and all accepted articles appear in the next issue to press.
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