Hippocampal Polysynaptic Computation

Neural circuitry is a self-organizing arithmetic device that converts input to output and thereby remodels its computational algorithm to produce more desired output; however, experimental evidence regarding the mechanism by which information is modified and stored while propagating across polysynaptic networks is sparse. We used functional multineuron calcium imaging to monitor the spike outputs from thousands of CA1 neurons in response to the stimulation of two independent sites of the dentate gyrus in rat hippocampal networks ex vivo. Only pyramidal cells were analyzed based on post hoc immunostaining. Some CA1 pyramidal cells were observed to fire action potentials only when both sites were simultaneously stimulated (AND-like neurons), whereas other neurons fired in response to either site of stimulation but not to concurrent stimulation (XOR-like neurons). Both types of neurons were interlaced in the same network and altered their logical operation depending on the timing of paired stimulation. Repetitive paired stimulation for brief periods induced a persistent reorganization of AND and XOR operators, suggesting a flexibility in parallel distributed processing. We simulated these network functions in silico and found that synaptic modification of the CA3 recurrent excitation is pivotal to the shaping of logic plasticity. This work provides new insights into how microscopic synaptic properties are associated with the mesoscopic dynamics of complex microcircuits.

[1]  Norio Matsuki,et al.  Fast and accurate detection of action potentials from somatic calcium fluctuations. , 2008, Journal of neurophysiology.

[2]  H. Markram,et al.  Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs , 1997, Science.

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

[4]  Rie Kimura,et al.  Integrative spike dynamics of rat CA1 neurons: a multineuronal imaging study , 2006, The Journal of physiology.

[5]  James L. McClelland,et al.  Explorations in Parallel Distributed Processing - Macintosh version: A Handbook of Models, Programs, and Exercises , 1989 .

[6]  A. Treves,et al.  Distinct Ensemble Codes in Hippocampal Areas CA3 and CA1 , 2004, Science.

[7]  J. Deuchars,et al.  CA1 pyramid-pyramid connections in rat hippocampus in vitro: Dual intracellular recordings with biocytin filling , 1996, Neuroscience.

[8]  W. Scoville,et al.  LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS , 1957, Journal of neurology, neurosurgery, and psychiatry.

[9]  J J Hopfield,et al.  Neural networks and physical systems with emergent collective computational abilities. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. Knierim,et al.  Comparison of population coherence of place cells in hippocampal subfields CA1 and CA3 , 2004, Nature.

[11]  Henry Markram,et al.  Real-Time Computing Without Stable States: A New Framework for Neural Computation Based on Perturbations , 2002, Neural Computation.

[12]  Dean V Buonomano,et al.  Timing of neural responses in cortical organotypic slices , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[13]  G. Bi,et al.  Distributed synaptic modification in neural networks induced by patterned stimulation , 1999, Nature.

[14]  Yuji Ikegaya,et al.  Synfire Chains and Cortical Songs: Temporal Modules of Cortical Activity , 2004, Science.

[15]  Rie Kimura,et al.  A low-cost method for brain slice cultures. , 2007, Journal of pharmacological sciences.

[16]  N. Matsuki,et al.  Metastability of Active CA3 Networks , 2007, The Journal of Neuroscience.

[17]  James J. Knierim,et al.  Ensemble Dynamics of Hippocampal Regions CA3 and CA1 , 2004, Neuron.

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

[19]  Norio Matsuki,et al.  Action-Potential Modulation During Axonal Conduction , 2011, Science.

[20]  Tim P Vogels,et al.  Signal Propagation and Logic Gating in Networks of Integrate-and-Fire Neurons , 2005, The Journal of Neuroscience.

[21]  Norio Matsuki,et al.  Watching neuronal circuit dynamics through functional multineuron calcium imaging (fMCI) , 2007, Neuroscience Research.

[22]  Stefan Leutgeb,et al.  Pattern separation, pattern completion, and new neuronal codes within a continuous CA3 map. , 2007, Learning & memory.

[23]  Jeffrey L. Elman,et al.  Finding Structure in Time , 1990, Cogn. Sci..

[24]  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.

[25]  C. Koch,et al.  Invariant visual representation by single neurons in the human brain , 2005, Nature.

[26]  D. Kullmann,et al.  Long-term synaptic plasticity in hippocampal interneurons , 2007, Nature Reviews Neuroscience.

[27]  Eugene M. Izhikevich,et al.  Which model to use for cortical spiking neurons? , 2004, IEEE Transactions on Neural Networks.

[28]  J. Guzowski,et al.  Differences in Hippocampal Neuronal Population Responses to Modifications of an Environmental Context: Evidence for Distinct, Yet Complementary, Functions of CA3 and CA1 Ensembles , 2004, The Journal of Neuroscience.

[29]  J. O'Keefe,et al.  The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat. , 1971, Brain research.