scholarly journals Recurrent Network Dynamics; a Link between Form and Motion

Author(s):  
Jeroen Joukes ◽  
Yunguo Yu ◽  
Jonathan D. Victor ◽  
Bart Krekelberg
2013 ◽  
Vol 16 (2) ◽  
pp. 227-234 ◽  
Author(s):  
Riccardo Beltramo ◽  
Giulia D'Urso ◽  
Marco Dal Maschio ◽  
Pasqualina Farisello ◽  
Serena Bovetti ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Destinee A. Aponte ◽  
Gregory Handy ◽  
Amber M. Kline ◽  
Hiroaki Tsukano ◽  
Brent Doiron ◽  
...  

AbstractDetecting the direction of frequency modulation (FM) is essential for vocal communication in both animals and humans. Direction-selective firing of neurons in the primary auditory cortex (A1) has been classically attributed to temporal offsets between feedforward excitatory and inhibitory inputs. However, it remains unclear how cortical recurrent circuitry contributes to this computation. Here, we used two-photon calcium imaging and whole-cell recordings in awake mice to demonstrate that direction selectivity is not caused by temporal offsets between synaptic currents, but by an asymmetry in total synaptic charge between preferred and non-preferred directions. Inactivation of cortical somatostatin-expressing interneurons (SOM cells) reduced direction selectivity, revealing its cortical contribution. Our theoretical models showed that charge asymmetry arises due to broad spatial topography of SOM cell-mediated inhibition which regulates signal amplification in strongly recurrent circuitry. Together, our findings reveal a major contribution of recurrent network dynamics in shaping cortical tuning to behaviorally relevant complex sounds.


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
N. V. Kartheek Medathati ◽  
James Rankin ◽  
Andrew I. Meso ◽  
Pierre Kornprobst ◽  
Guillaume S. Masson

2021 ◽  
Author(s):  
Shogo Ohmae ◽  
Keiko Ohmae ◽  
Shane A Heiney ◽  
Divya Subramanian ◽  
Javier F Medina

The neural architecture of the cerebellum is thought to be specialized for performing supervised learning: specific error-related climbing fiber inputs are used to teach sensorimotor associations to small ensembles of Purkinje cells located in functionally distinct modules that operate independently of each other in a purely feedforward manner. Here, we test whether the basic operation of the cerebellum complies with this basic architecture in mice that learned a simple sensorimotor association during eyeblink conditioning. By recording Purkinje cells in different modules and testing whether their responses rely on recurrent circuits, our results reveal three operational principles about the functional organization of the cerebellum that stand in stark contrast to the conventional view: (1) Antagonistic organization, (2) Recurrent network dynamics, and (3) Intermodular communication. We propose that the neural architecture of the cerebellum implements these three operational principles to achieve optimal performance and solve a number of problems in motor control.


2010 ◽  
Vol 22 (3) ◽  
pp. 621-659 ◽  
Author(s):  
Bryan P. Tripp ◽  
Chris Eliasmith

Temporal derivatives are computed by a wide variety of neural circuits, but the problem of performing this computation accurately has received little theoretical study. Here we systematically compare the performance of diverse networks that calculate derivatives using cell-intrinsic adaptation and synaptic depression dynamics, feedforward network dynamics, and recurrent network dynamics. Examples of each type of network are compared by quantifying the errors they introduce into the calculation and their rejection of high-frequency input noise. This comparison is based on both analytical methods and numerical simulations with spiking leaky-integrate-and-fire (LIF) neurons. Both adapting and feedforward-network circuits provide good performance for signals with frequency bands that are well matched to the time constants of postsynaptic current decay and adaptation, respectively. The synaptic depression circuit performs similarly to the adaptation circuit, although strictly speaking, precisely linear differentiation based on synaptic depression is not possible, because depression scales synaptic weights multiplicatively. Feedback circuits introduce greater errors than functionally equivalent feedforward circuits, but they have the useful property that their dynamics are determined by feedback strength. For this reason, these circuits are better suited for calculating the derivatives of signals that evolve on timescales outside the range of membrane dynamics and, possibly, for providing the wide range of timescales needed for precise fractional-order differentiation.


2018 ◽  
Author(s):  
Rich Pang ◽  
Adrienne Fairhall

AbstractCognitive flexibility, the adaptation of mental processing to changes in task demands, is thought to depend on biological neural networks’ ability to rapidly modulate the dynamics governing how they process information. While extensive work has elucidated how network dynamics can be reshaped by slowly occurring structural changes, e.g. the gradual modification of recurrent synaptic patterns, much less is known about how dynamics might be reconfigured over faster timescales of seconds. One compelling example of rapid and selective modulation of network dynamics potentially involved in cognitive flexibility is observed in rodent hippocampus, where short bouts of exploratory behavior cause new activity sequences to preferentially “replay” during subsequent awake rest periods without continued sensory input. Fast mechanisms for selectively biasing sequential activity through networks, however, remain unknown. Using a spiking neural network model, we asked whether a simplified version of sequence replay could arise from three biophysically plausible components: recurrent, spatially organized connectivity; homogeneous, stochastic “gating” inputs; and rapid, activity-dependent scaling of gating input strengths, based on a phenomenon known as long-term potentiation of intrinsic excitability (LTP-IE). Indeed, these enabled both forward and reverse replay of flexible sequences reflecting recent behavior, despite unchanged recurrent weights. Specifically, activation-triggered LTP-IE “tags” neurons in the recurrent network by increasing their spiking probability when gating input is applied, and the sequential ordering of spikes is reconstructed by the existing recurrent connectivity. In a proof-of-concept demonstration, we also show how LTP-IE-based sequences can implement temporary stimulus-response mappings in a straightforward manner. These results elucidate a simple yet previously unexplored combination of biological mechanisms that converge in hippocampus and suffice for fast and flexible reconfiguration of sequential network dynamics, suggesting their potential role in cognitive flexibility over rapid timescales.


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