Koizumi Amane, Takayasu Misako, Takayasu Hideki
Division of Correlative Physiology, National Institute for Physiological Sciences, Okazaki, Japan.
J Integr Neurosci. 2010 Sep;9(3):337-50. doi: 10.1142/s0219635210002469.
In this paper, we found that spatial and temporal asymmetricity of excitatory connections are able to generate directional selectivity which can be enhanced by asymmetrical inhibitory connections by reconstructing a hexagonally-arranged three-layered simulation model of retina by NEURON simulator. Asymmetric excitatory inputs to ganglion cells with randomly arborizing dendrites were able to generate weaker directional selectivity to moving stimuli whose speed was less than 10 μm/msec. By just adding asymmetric inhibitory connections via inhibitory amacrine cells, directional selectivity became stronger to respond to moving stimuli at ten times faster speed (< 100 μm/msec). In conclusion, an excitatory mechanism appeared to generate directional selectivity while asymmetric inhibitory connections enhance directional selectivity in retina.
在本文中,我们通过NEURON模拟器重建了一个六边形排列的三层视网膜模拟模型,发现兴奋性连接的时空不对称性能够产生方向选择性,并且不对称抑制性连接可以增强这种方向选择性。对具有随机分支树突的神经节细胞的不对称兴奋性输入,能够对速度小于10μm/毫秒的移动刺激产生较弱的方向选择性。仅通过抑制性无长突细胞添加不对称抑制性连接后,对速度快十倍(<100μm/毫秒)的移动刺激的方向选择性变得更强。总之,兴奋性机制似乎产生方向选择性,而不对称抑制性连接则增强视网膜中的方向选择性。