Abstract
Recently reported experimental findings suggest that the hippocampal CA1 network stores spatio-temporal spike patterns and retrieves temporally reversed and spread-out patterns. In this paper, we explore the idea that the properties of the neural interactions and the synaptic plasticity rule in the CA1 network enable it to function as a hetero-associative memory recalling such reversed and spread-out spike patterns. In line with Lengyel’s speculation (Lengyel et al., 2005), we firstly derive optimally designed spike-timing-dependent plasticity (STDP) rules that are matched to neural interactions formalized in terms of phase response curves (PRCs) for performing the hetero-associative memory function. By maximizing object functions formulated in terms of mutual information for evaluating memory retrieval performance, we search for STDP window functions that are optimal for retrieval of normal and doubly spread-out patterns under the constraint that the PRCs are those of CA1 pyramidal neurons. The system, which can retrieve normal and doubly spread-out patterns, can also retrieve reversed patterns with the same quality. Finally, we demonstrate that purposely designed STDP window functions qualitatively conform to typical ones found in CA1 pyramidal neurons.
Highlights
It has been reported that characteristic ensemble spiking patterns are consistently repeated in the hippocampal CA1 region during waking and sleep periods [1,2,3,4,5,6,7,8,9]
Under the speculation that a phase response curve (PRC) is appropriate to formulate the neural interactions if memories are embedded by spike-timing-dependent plasticity (STDP), they derived pairs of STDP window functions and phase response curves (PRCs) optimally functioning as an auto-associative memory
They showed that the features of the PRCs of hippocampal CA3 pyramidal neurons qualitatively conform to ones theoretically derived from typical STDP window functions
Summary
It has been reported that characteristic ensemble spiking patterns are consistently repeated in the hippocampal CA1 region during waking and sleep periods [1,2,3,4,5,6,7,8,9]. Foster and Wilson (2006) reported that the spike patterns observed during running periods are reproduced in a temporally reversed order during rest periods [9] These experiments suggest that the CA1 network stores spatio-temporal spike patterns and retrieves reversed and spread-out patterns. Under the speculation that a phase response curve (PRC) is appropriate to formulate the neural interactions if memories are embedded by spike-timing-dependent plasticity (STDP), they derived pairs of STDP window functions and PRCs optimally functioning as an auto-associative memory. They showed that the features of the PRCs of hippocampal CA3 pyramidal neurons qualitatively conform to ones theoretically derived from typical STDP window functions. The possible existence of STDP at recurrent synapses between CA3 pyramidal neurons has been suggested [11,12], as far as we know, there are no reports on capturing the entire shape of the STDP window function
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