Samsonovich A, McNaughton B L
Arizona Research Laboratories Division of Neural Systems, Memory and Aging, The University of Arizona, Tucson, Arizona 85749, USA.
J Neurosci. 1997 Aug 1;17(15):5900-20. doi: 10.1523/JNEUROSCI.17-15-05900.1997.
A minimal synaptic architecture is proposed for how the brain might perform path integration by computing the next internal representation of self-location from the current representation and from the perceived velocity of motion. In the model, a place-cell assembly called a "chart" contains a two-dimensional attractor set called an "attractor map" that can be used to represent coordinates in any arbitrary environment, once associative binding has occurred between chart locations and sensory inputs. In hippocampus, there are different spatial relations among place fields in different environments and behavioral contexts. Thus, the same units may participate in many charts, and it is shown that the number of uncorrelated charts that can be encoded in the same recurrent network is potentially quite large. According to this theory, the firing of a given place cell is primarily a cooperative effect of the activity of its neighbors on the currently active chart. Therefore, it is not particularly useful to think of place cells as encoding any particular external object or event. Because of its recurrent connections, hippocampal field CA3 is proposed as a possible location for this "multichart" architecture; however, other implementations in anatomy would not invalidate the main concepts. The model is implemented numerically both as a network of integrate-and-fire units and as a "macroscopic" (with respect to the space of states) description of the system, based on a continuous approximation defined by a system of stochastic differential equations. It provides an explanation for a number of hitherto perplexing observations on hippocampal place fields, including doubling, vanishing, reshaping in distorted environments, acquiring directionality in a two-goal shuttling task, rapid formation in a novel environment, and slow rotation after disorientation. The model makes several new predictions about the expected properties of hippocampal place cells and other cells of the proposed network.
本文提出了一种最小化的突触架构,用于解释大脑如何通过根据当前自身位置的表征以及感知到的运动速度来计算下一个自身位置的内部表征,从而实现路径整合。在该模型中,一个名为“图表”的位置细胞集合包含一个名为“吸引子地图”的二维吸引子集合,一旦图表位置与感觉输入之间发生关联绑定,该吸引子地图就可用于表示任意环境中的坐标。在海马体中,不同环境和行为背景下的位置场之间存在不同的空间关系。因此,相同的神经元单元可能参与多个图表,并且研究表明,在同一个递归网络中能够编码的不相关图表数量可能相当大。根据这一理论,给定位置细胞的放电主要是其相邻细胞在当前活跃图表上活动的协同效应。因此,将位置细胞视为编码任何特定外部物体或事件并不是特别有用。由于其递归连接,海马体CA3区被认为是这种“多图表”架构的可能位置;然而,解剖学上的其他实现方式并不会使主要概念无效。该模型通过积分发放单元网络进行数值实现,同时基于由随机微分方程系统定义的连续近似,对系统进行“宏观”(相对于状态空间)描述。它为迄今为止关于海马体位置场的一些令人困惑的观察结果提供了解释,包括位置场翻倍、消失、在扭曲环境中重塑、在双目标穿梭任务中获得方向性、在新环境中快速形成以及在方向迷失后缓慢旋转。该模型对海马体位置细胞以及所提出网络中其他细胞的预期特性做出了一些新的预测。