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Development of a detailed model of calcium dynamics at the postsynaptic spine of an excitatory synapse

机译:兴奋性突触的突触后脊柱钙动力学详细模型的建立

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Postsynaptic calcium dynamics play a critical role in synaptic plasticity, but are often difficult to measure in experimental protocols due to their relatively fast rise and decay times, and the small spine dimensions. To circumvent these limitations, we propose to develop a computational model of calcium dynamics in the postsynaptic spine. This model integrates the main elements that participate in calcium concentration influx, efflux, diffusion and buffering. These consist of (i) spine geometry; (ii) calcium influx through NMDA receptors and voltage-dependent calcium channels (VDCC); (iii) calcium efflux with plasma membrane calcium pumps (PMCA) and sodium-calcium exchangers (NCX); (iv) intracellular calcium stores; and (v) calcium buffers. We herein present computational results we obtained and compare them with experimentally measured data, thereby validating the proposed model. Overall the development of such postsynaptic calcium model may help us better understand the intricacies of interplay between the different elements that shape calcium dynamics and impact synaptic plasticity in normal functions and pathologies. This model also constitutes a first step in the development of a nonlinear input-output calcium dynamics model for multi-scale, large scale neuronal simulations.
机译:突触后钙动力学在突触可塑性中起着至关重要的作用,但由于其相对较快的上升和下降时间以及较小的脊柱尺寸,因此在实验方案中通常难以测量。为了避免这些局限性,我们建议建立突触后脊柱中钙动力学的计算模型。该模型整合了参与钙浓度流入,流出,扩散和缓冲的主要元素。这些包括:(i)脊柱的几何形状; (ii)钙通过NMDA受体和电压依赖性钙通道(VDCC)流入; (iii)通过质膜钙泵(PMCA)和钠钙交换器(NCX)进行钙流出; (iv)细胞内钙储存; (v)钙缓冲剂。我们在这里介绍了我们获得的计算结果,并将其与实验测量的数据进行比较,从而验证了所提出的模型。总体而言,这种突触后钙模型的发展可能有助于我们更好地理解影响钙动力学并影响正常功能和病理状态下突触可塑性的不同元素之间相互作用的复杂性。该模型还构成了用于多尺度,大规模神经元模拟的非线性输入-输出钙动力学模型开发的第一步。

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