Intrafaculty College of Medical Informatics and Biostatistics, Medical University of Gdańsk, 1 Debinki St., 80-211 Gdańsk, Poland.
Department of Anatomy and Neurobiology, Medical University of Gdańsk, 1 Debinki St., 80-211 Gdańsk, Poland.
Molecules. 2019 May 17;24(10):1909. doi: 10.3390/molecules24101909.
This paper aims to present computer modeling of synaptic plasticity and memory in the CA3-CA1 hippocampal formation microcircuit. The computer simulations showed a comparison of a pathological model in which Alzheimer's disease (AD) was simulated by synaptic degradation in the hippocampus and control model (healthy) of CA3-CA1 networks with modification of weights for the memory. There were statistically higher spike values of both CA1 and CA3 pyramidal cells in the control model than in the pathological model (p = 0.0042 for CA1 and p = 0.0033 for CA3). A similar outcome was achieved for frequency (p = 0.0002 for CA1 and p = 0.0001 for CA3). The entropy of pyramidal cells of the healthy CA3 network seemed to be significantly higher than that of AD (p = 0.0304). We need to study a lot of physiological parameters and their combinations of the CA3-CA1 hippocampal formation microcircuit to understand AD. High statistically correlations were obtained between memory, spikes and synaptic deletion in both CA1 and CA3 cells.
本文旨在对 CA3-CA1 海马结构微电路中的突触可塑性和记忆进行计算机建模。计算机模拟比较了一个病理模型(通过海马突触退化模拟阿尔茨海默病 (AD))和一个对照模型(健康)的 CA3-CA1 网络,后者对记忆的权重进行了修改。在对照模型中,CA1 和 CA3 锥体神经元的尖峰值均明显高于病理模型(CA1 为 p = 0.0042,CA3 为 p = 0.0033)。频率也得到了类似的结果(CA1 为 p = 0.0002,CA3 为 p = 0.0001)。健康 CA3 网络的锥体细胞的熵似乎明显高于 AD(p = 0.0304)。我们需要研究大量的生理参数及其组合,以了解 CA3-CA1 海马结构微电路中的 AD。在 CA1 和 CA3 细胞中,记忆、尖峰和突触缺失之间都得到了高度的统计学相关性。