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Research Article

Learning rules and network repair in spike-timing-based computation networks

J. J. Hopfield and Carlos D. Brody
PNAS January 6, 2004 101 (1) 337-342; https://doi.org/10.1073/pnas.2536316100
J. J. Hopfield
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Carlos D. Brody
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  1. Contributed by J. J. Hopfield, October 1, 2003

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    Fig. 1.

    Spiking network model of odor recognition. (Upper) Spike rasters of all presynaptic cells during a single trial (a sniff of the target odor). Spikes from cells that do and do not have a functional connection to the postsynaptic cell are shown in red and blue, respectively. Different presynaptic cells receive different peak currents during the odor sniff. Cells have been sorted vertically by the magnitude of that peak current. Vertical red lines indicate postsynaptic cell firing times. The essence of the self-repair problem is to automatically determine whether a presynaptic spike train belongs to the blue or the red raster set and, therefore, whether the presynaptic cell producing it should have a functional connection to the postsynaptic cell. A common underlying subthreshold oscillation promotes a systematic relationship between injected current and phase of firing of the presynaptic cells (indicated by the gray background). For any odor, there is a subset of presynaptic cells that, at the peak of the sniff, will fire at the same phase with respect to the oscillation, will therefore be synchronized, and can be used to drive an odor-selective postsynaptic cell (3). (Lower) The strength of the stimulus during the sniff is plotted.

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    Fig. 2.

    (a) The weights wk after training on the classification problem, plotted against the time difference Δt of the post- and presynaptic spike pairs. Dots indicate an evaluation of the weights based on the spike trains from a single stimulus presentation. The solid line is a spline fit through wk points averaged over 16 runs, and it should closely approximate the function W(Δt). In the training set used, there were ≈1,000 appropriate presynaptic spike train examples and 4,600 inappropriate spike train examples. (b) Histogram of the number of training set examples having estimated probability P of belonging to the appropriate class (determined by using the wk shown in a and Eqs. 2 and 3). The known appropriate and inappropriate spike trains are shown. The vertical dashed line indicates the cutoff threshold for P, defining the topranked presynaptic cells for making functional connections. (c and d) For the olfactory network, selective odor recognition corresponds to choosing connections from cells with a narrow range of peak input currents, as compared with the total possible range. We plot the estimated probability P as a function of the peak input current of the presynaptic cells. Choosing cells with an estimated P above the threshold setting (indicated by the dashed line in c and d) also chooses cells with peak currents within a narrow range. In general, such an underlying principle allowing visualization in plots such as those in c and d might not be known.

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    Fig. 4.

    The problem of drift with STDP rules. (a) Schematic of a linear array of neurons, indexed by k, that each fire at a time t = k + η, where η is jitter due to noise. All of these neurons could potentially make connections to the postsynaptic neuron shown above them, but initially only a small subset, with almost synchronous firing times, makes a functional connection, as shown. (b) The gray line indicates the initial density of connections from presynaptic cells to the postsynaptic cell. Presynaptic cells are labeled by their mean firing time, in ms. The arrow indicates the firing time of the postsynaptic cell. Black lines show the connection densities resulting from two successive iterations of the self-repair procedure, using the rule shown as a solid line in c.(c) The solid line shows a purely causal (all positive in the Δt > 0 region, all negative in the Δt < 0 region) plasticity rule. (This plasticity rule is used in b, where it is shown that it leads to strong drift.) The dotted line is the same learning rule but shifted 2 ms toward the negative Δt region. (d) Same format as in c, showing initial connection density and two iterations of self-repair, but now using the plasticity rule shown as a dashed line in panel c. Drift is sharply reduced.

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    Fig. 3.

    Histograms of the number of odors producing n spikes in the postsynaptic cell; 499 random odors plus the postsynaptic cell's target odor were used. (a) Responses using the original, engineered connections are shown (3). (b) Responses using the connections produced after one iteration of complete functional connection replacement are shown. (c) Original response of a broadly tuned postsynaptic cell connected to five presynaptic cells to the presentation of 500 random odors. It responded with 11 spikes to one of the odors. (d) With learning (one iteration) turned on, when some particular odor drove the broadly tuned cell to produce 11 spikes, the synapses were remodeled. This remodeling led to the odor selectivity shown. The odor that triggered the synaptic change now produces many spikes, but all other odors produce very little response. The triggering odor has become the target odor of a highly selective cell.

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Learning rules and network repair in spike-timing-based computation networks
J. J. Hopfield, Carlos D. Brody
Proceedings of the National Academy of Sciences Jan 2004, 101 (1) 337-342; DOI: 10.1073/pnas.2536316100

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Learning rules and network repair in spike-timing-based computation networks
J. J. Hopfield, Carlos D. Brody
Proceedings of the National Academy of Sciences Jan 2004, 101 (1) 337-342; DOI: 10.1073/pnas.2536316100
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Proceedings of the National Academy of Sciences: 101 (1)
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  • Article
    • Abstract
    • A Functioning Network for Studying the Repair Problem
    • Deriving the Repair Rule
    • Applying the Repair Rule: Functional Properties of a Network Composed of Fully Replaced Synapses
    • Single-Trial Unsupervised Learning
    • Long-Term Stability
    • Conclusion
    • Acknowledgments
    • Footnotes
    • References
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