Abstract

Recent studies have proposed that the diffusion of messenger molecules, such as monoamines, can mediate the plastic adaptation of synapses in supervised learning of neural networks. Based on these findings we developed a model for neural learning, where the signal for plastic adaptation is assumed to propagate through the extracellular space. We investigate the conditions allowing learning of Boolean rules in a neural network. Even fully excitatory networks show very good learning performances. Moreover, the investigation of the plastic adaptation features optimizing the performance suggests that learning is very sensitive to the extent of the plastic adaptation and the spatial range of synaptic connections.

Highlights

  • Recent studies have proposed that the diffusion of messenger molecules, such as monoamines, can mediate the plastic adaptation of synapses in supervised learning of neural networks

  • The investigation of the plastic adaptation features optimizing the performance suggests that learning is very sensitive to the extent of the plastic adaptation and the spatial range of synaptic connections

  • Different studies have proposed a variety of models for a neural network able to learn without passing error gradients antidromically

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Summary

Spatial features of synaptic adaptation affecting learning performance

Recent studies have proposed that the diffusion of messenger molecules, such as monoamines, can mediate the plastic adaptation of synapses in supervised learning of neural networks Based on these findings we developed a model for neural learning, where the signal for plastic adaptation is assumed to propagate through the extracellular space. In this article we extend these ideas by a model, where the strength of the feedback signal does not depend on a network distance, but on the euclidean distance By this model we study the importance of the localization of a teaching signal, i.e. if a localized learning signal can represent advantages over one acting widely in space. This is the case, for instance, of dopamine whose effect covers a finite range of tens to thousands of synapses[13]

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