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Simulation of an inner plexiform layer neural circuit in vertebrate retina leads to sustained and transient excitation

机译:脊椎动物视网膜内丛状神经回路的仿真导致持续和短暂的兴奋

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The conversion of sustained into transient responses to a step of light in the visual system is first accomplished at the amacrine cells in the vertebrate retina. Neurobiological data from the vertebrate retina have provided some of the key synaptic connections between bipolar and amacrine cells that are thought to underlie the formation of transient and sustained amacrine cell responses to light. Using a neural network model that incorporates data from patch clamp recording techniques in the retinal slice preparation, we have constructed and simulated a connectionist model of the local circuits within the inner plexiform layer of the vertebrate retina that leads to the conversion of sustained to transient excitatory signals similar to those observed in retinal amacrine cells. The model incorporates sustained glutamate release from bipolar cells, GABA(sub)B feedback to bipolar cell axon terminals, GABA(sub)A feedforward input from sustained to transient amacrine cells, and rapidly desensitizing glutamate receptors in the transient amacrine cell.
机译:视觉系统中对光阶的持续响应到瞬态响应的转换首先在脊椎动物视网膜中的无长突细胞处完成。来自脊椎动物视网膜的神经生物学数据已经提供了双极和无长突细胞之间的一些关键突触连接,这些突触连接被认为是对光产生瞬时和持续的无长突细胞反应的基础。我们使用一个神经网络模型,该模型将来自膜片钳记录技术的数据整合到视网膜切片制备中,我们构建并模拟了脊椎动物视网膜内丛状层内局部回路的连接模型,该模型导致持续性兴奋性向短暂性兴奋性的转化信号类似于在视网膜无长突细胞中观察到的信号。该模型包括从双极细胞持续释放谷氨酸,向双极细胞轴突末端的GABA(sub)B反馈,从持续无源无长突细胞向持续无源Amacrine细胞的GABA(sub)A前馈输入,以及瞬变无长突细胞中的谷氨酸受体快速脱敏。

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