首页> 美国卫生研究院文献>Entropy >Effects of Inducing Gamma Oscillations in Hippocampal Subregions DG CA3 and CA1 on the Potential Alleviation of Alzheimer’s Disease-Related Pathology: Computer Modeling and Simulations
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Effects of Inducing Gamma Oscillations in Hippocampal Subregions DG CA3 and CA1 on the Potential Alleviation of Alzheimer’s Disease-Related Pathology: Computer Modeling and Simulations

机译:诱导γ振荡在海马次区DGCA3和CA1中对阿尔茨海默病相关病理学潜在缓解的影响:计算机建模与模拟

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摘要

The aim of this study was to evaluate the possibility of the gamma oscillation function (40–130 Hz) to reduce Alzheimer’s disease related pathology in a computer model of the hippocampal network dentate gyrus, CA3, and CA1 (DG-CA3-CA1) regions. Methods: Computer simulations were made for a pathological model in which Alzheimer’s disease was simulated by synaptic degradation in the hippocampus. Pathology modeling was based on sequentially turning off the connections with entorhinal cortex layer 2 (EC2) and the dentate gyrus on CA3 pyramidal neurons. Gamma induction modeling consisted of simulating the oscillation provided by the septo-hippocampal pathway with band frequencies from 40–130 Hz. Pathological models with and without gamma induction were compared with a control. Results: In the hippocampal regions of DG, CA3, and CA1, and jointly DG-CA3-CA1 and CA3-CA1, gamma induction resulted in a statistically significant improvement in terms of increased numbers of spikes, spikes per burst, and burst duration as compared with the model simulating Alzheimer’s disease (AD). The positive maximal Lyapunov exponent was negative in both the control model and the one with gamma induction as opposed to the pathological model where it was positive within the DG-CA3-CA1 region. Gamma induction resulted in decreased transfer entropy in accordance with the information flow in DG → CA3 and CA3 → CA1. Conclusions: The results of simulation studies show that inducing gamma oscillations in the hippocampus may reduce Alzheimer’s disease related pathology. Pathologically higher transfer entropy values after gamma induction returned to values comparable to the control model.
机译:本研究的目的是评估γ振荡功能(40-130Hz)的可能性,以减少海马网络牙齿,CA3和CA1(DG-CA3-CA1)区的计算机模型中的阿尔茨海默病相关病理学。方法:采用海马突触降解模拟阿尔茨海默病的病理模型进行了计算机仿真。病理学建模是基于依次关闭与Entorthinal皮质层2(EC2)的连接和Ca3金字塔神经元的牙齿转象。 Gamma诱导建模包括模拟由40-130 Hz的带频率提供的侧面海马通路提供的振荡。将病理模型与无γ诱导进行比较。结果:在DG,CA3和CA1的海马区域,并共同DG-CA3-CA1和CA3-CA1,γ诱导导致尖刺数量增加,每次突发的尖峰和突发持续时间的统计上显着改善与模拟Alzheimer疾病(广告)的模型相比。对照模型和具有伽马诱导的阳性最大Lyapunov指数在DG-CA3-CA1区域内的病理模型相反,阳性最大Lyapunov指数是负的。根据DG→CA3和CA3→CA1中的信息流导致伽马诱导导致转移熵减少。结论:模拟研究结果表明,诱导海马γ振荡可能降低阿尔茨海默病相关病理学。伽马诱导返回到与控制模型相当的值后的病理上更高的转移熵值。

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