Pham Duy-Tan J, Bouteiller Jean-Marie C
Center for Neural Engineering, Alfred E. Mann Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles, CA 90007, USA.
Neural Systems Computational Modeling Lab, Alfred E. Mann Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles, CA 90007, USA.
Biomedicines. 2025 Jul 8;13(7):1674. doi: 10.3390/biomedicines13071674.
: The N-methyl-d-aspartate receptor (NMDA-R) is a glutamate ionotropic receptor in the brain that is crucial for synaptic plasticity, which underlies learning and memory formation. Dysfunction of NMDA receptors is implicated in various neurological diseases due to their roles in both normal cognition and excitotoxicity. However, their dynamics are challenging to capture accurately due to their high complexity and non-linear behavior. : This article presents the elaboration and calibration of experimentally constrained computational models of GluN1/GluN2A NMDA-R dynamics: (1) a nine-state kinetic model optimized to replicate experimental data and (2) a computationally efficient look-up table model capable of replicating the dynamics of the nine-state kinetic model with a highly reduced footprint. Determination of the kinetic model's parameter values was performed using the particle swarm optimization algorithm. The optimized kinetic model was then used to generate a rich input-output dataset to train the look-up table synapse model and estimate its coefficients. : Optimization produced a kinetic model capable of accurately reproducing experimentally found results such as frequency-dependent potentiation and the temporal response due to synaptic release of glutamate. Furthermore, the look-up table synapse model was able to closely mimic the dynamics of the optimized kinetic model. : The results obtained with both models indicate that they constitute accurate alternatives for faithfully reproducing the dynamics of NMDA-Rs. High computational efficiency is also achieved with the use of the look-up table synapse model, making this implementation an ideal option for inclusion in large-scale neuronal models.
N-甲基-D-天冬氨酸受体(NMDA-R)是大脑中的一种谷氨酸离子型受体,对突触可塑性至关重要,而突触可塑性是学习和记忆形成的基础。由于NMDA受体在正常认知和兴奋性毒性中都发挥作用,其功能障碍与多种神经疾病有关。然而,由于其高度复杂性和非线性行为,准确捕捉它们的动力学具有挑战性。
本文介绍了对GluN1/GluN2A NMDA-R动力学的实验约束计算模型的细化和校准:(1)一个经过优化以复制实验数据的九态动力学模型,以及(2)一个计算效率高的查找表模型,该模型能够以大幅减少的占用空间复制九态动力学模型的动力学。使用粒子群优化算法确定动力学模型的参数值。然后使用优化后的动力学模型生成丰富的输入-输出数据集,以训练查找表突触模型并估计其系数。
优化产生了一个能够准确再现实验结果的动力学模型,如频率依赖性增强和谷氨酸突触释放引起的时间响应。此外,查找表突触模型能够紧密模仿优化后的动力学模型的动力学。
这两个模型获得的结果表明,它们是忠实地再现NMDA-R动力学的准确替代方案。使用查找表突触模型还实现了高计算效率,使其成为纳入大规模神经元模型的理想选择。