Volume 12 Supplement 1

Twentieth Annual Computational Neuroscience Meeting: CNS*2011

Open Access

Different neural codes result in bidirectional connectivity formed by the same model of spike-timing-dependent plasticity

BMC Neuroscience201112(Suppl 1):P247

DOI: 10.1186/1471-2202-12-S1-P247

Published: 18 July 2011

Recent studies on phenomenological models of spike-timing-dependent plasticity (STDP) extend the idea of a pure spike-based paradigm to the level of dendritic voltage [1]. In such models, the decision to induce early long-term potentiation (eLTP) or long-term depression (eLTD) not solely depends on the time difference between pre- and post-synaptic spikes but also on the precise dynamics of the post-synaptic potential. From simulations of small neural networks and different stimulation schemes corresponding to different neural codes, these studies have concluded that the pattern of synaptic connectivity would directly follow from the neural code and vice versa. For example, they have suggested that strong uni-directional connectivity would emerge through temporal coding, whereas bidirectional connectivity would be indicative for a rate code. Relying on results from earlier studies on first generation STDP models [24], synchronous temporal codes forming bidirectional connectivity patterns were considered unlikely in [1]. However, recent findings revise a general exclusion of this relationship [5] even for first generation STDP models. In particular, our work shows that realistic STDP models as proposed in [1] can actually not predict the neural code (temporal vs. rate coding) by looking at the pattern of synaptic connectivity within a specific brain area. With the same kind of simulations as in [1], but additionally considering stimulation conditions for synchronous temporal coding, we show that bidirectional connections are still possible. Furthermore we discuss the influence of synchronization precision and oscillatory activity.

Authors’ Affiliations

Institute of Neural Information Processing, Ulm University
Honda Research Institute EU


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© Hauser et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.