Computational consequences of experimentally derived spike-time and weight dependent plasticity rules

We present two weight- and spike-time dependent synaptic plasticity rules consistent with the physiological data of Bi and Poo (J Neurosci 18:10464–10472, 1998). One rule assumes synaptic saturation, while the other is scale free. We extend previous analyses of the asymptotic consequences of weight-dependent STDP to the case of strongly correlated pre- and post-synaptic spiking, more closely resembling associative learning. We further provide a general formula for the contribution of any number of spikes to synaptic drift. Asymptotic weights are shown to principally depend on the correlation and rate of pre- and post-synaptic activity, decreasing with increasing rate under correlated activity, and increasing with rate under uncorrelated activity. Spike train statistics reveal a quantitative effect only in the pre-asymptotic regime, and we provide a new interpretation of the relation between BCM and STDP data.

[1]  Guo-Qiang Bi,et al.  Spatiotemporal specificity of synaptic plasticity: cellular rules and mechanisms , 2002, Biological Cybernetics.

[2]  S. Wang,et al.  Dissection of bidirectional synaptic plasticity into saturable unidirectional processes. , 2005, Journal of neurophysiology.

[3]  M. Bear,et al.  Homosynaptic long-term depression in area CA1 of hippocampus and effects of N-methyl-D-aspartate receptor blockade. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[4]  J. Hopfield,et al.  All-or-none potentiation at CA3-CA1 synapses. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Haim Sompolinsky,et al.  Learning Input Correlations through Nonlinear Temporally Asymmetric Hebbian Plasticity , 2003, The Journal of Neuroscience.

[6]  Y. Dan,et al.  Contribution of individual spikes in burst-induced long-term synaptic modification. , 2006, Journal of neurophysiology.

[7]  Mark C. W. van Rossum,et al.  Stable Hebbian Learning from Spike Timing-Dependent Plasticity , 2000, The Journal of Neuroscience.

[8]  D. Johnston,et al.  Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs , 1997 .

[9]  D. Debanne,et al.  Cooperative interactions in the induction of long-term potentiation and depression of synaptic excitation between hippocampal CA3-CA1 cell pairs in vitro. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Y. Dan,et al.  Spike-timing-dependent synaptic modification induced by natural spike trains , 2002, Nature.

[11]  David W. Nauen,et al.  Coactivation and timing-dependent integration of synaptic potentiation and depression , 2005, Nature Neuroscience.

[12]  P. J. Sjöström,et al.  Rate, Timing, and Cooperativity Jointly Determine Cortical Synaptic Plasticity , 2001, Neuron.

[13]  Eugene M. Izhikevich,et al.  Relating STDP to BCM , 2003, Neural Computation.

[14]  D. Debanne,et al.  Heterogeneity of Synaptic Plasticity at Unitary CA3–CA1 and CA3–CA3 Connections in Rat Hippocampal Slice Cultures , 1999, The Journal of Neuroscience.

[15]  Stefan Rotter,et al.  Higher-Order Statistics of Input Ensembles and the Response of Simple Model Neurons , 2003, Neural Computation.

[16]  S. Wang,et al.  Graded bidirectional synaptic plasticity is composed of switch-like unitary events. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[17]  M. Hasselmo Neuromodulation and cortical function: modeling the physiological basis of behavior , 1995, Behavioural Brain Research.

[18]  W. Levy,et al.  Temporal contiguity requirements for long-term associative potentiation/depression in the hippocampus , 1983, Neuroscience.

[19]  L. Abbott,et al.  Synaptic plasticity: taming the beast , 2000, Nature Neuroscience.

[20]  K. H. Britten,et al.  Power spectrum analysis of bursting cells in area MT in the behaving monkey , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  J. Leo van Hemmen,et al.  Modeling Synaptic Plasticity in Conjunction with the Timing of Pre- and Postsynaptic Action Potentials , 2000, Neural Computation.

[22]  E. Bienenstock,et al.  Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[23]  Daniel D. Lee,et al.  Equilibrium properties of temporally asymmetric Hebbian plasticity. , 2000, Physical review letters.

[24]  R. Kempter,et al.  Hebbian learning and spiking neurons , 1999 .

[25]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

[26]  G. Bi,et al.  Synaptic Modifications in Cultured Hippocampal Neurons: Dependence on Spike Timing, Synaptic Strength, and Postsynaptic Cell Type , 1998, The Journal of Neuroscience.

[27]  L. Abbott,et al.  Competitive Hebbian learning through spike-timing-dependent synaptic plasticity , 2000, Nature Neuroscience.

[28]  G. Lynch,et al.  Heterosynaptic depression: a postsynaptic correlate of long-term potentiation , 1977, Nature.

[29]  P. Pavlidis,et al.  Pair Recordings Reveal All-Silent Synaptic Connections and the Postsynaptic Expression of Long-Term Potentiation , 2001, Neuron.

[30]  Leon N. Cooper,et al.  A Biophysical Basis for the Inter-spike Interaction of Spike-timing-dependent Plasticity , 2006, Biological Cybernetics.

[31]  David B. Grayden,et al.  Spike-Timing-Dependent Plasticity: The Relationship to Rate-Based Learning for Models with Weight Dynamics Determined by a Stable Fixed Point , 2004, Neural Computation.

[32]  M. Bear,et al.  Experience-dependent modification of synaptic plasticity in visual cortex , 1996, Nature.