Sensorimotor encoding by synchronous neural ensemble activity at multiple levels of the somatosensory system

Science ◽  
1995 ◽  
Vol 268 (5215) ◽  
pp. 1353-1358 ◽  
Author(s):  
M. Nicolelis ◽  
L. Baccala ◽  
R. Lin ◽  
J. Chapin
1989 ◽  
Vol 9 (8) ◽  
pp. 2764-2775 ◽  
Author(s):  
H Eichenbaum ◽  
SI Wiener ◽  
ML Shapiro ◽  
NJ Cohen

2011 ◽  
Vol 467-469 ◽  
pp. 1291-1296
Author(s):  
Wen Wen Bai ◽  
Xin Tian

Working memory is one of important cognitive functions and recent studies demonstrate that prefrontal cortex plays an important role in working memory. But the issue that how neural activity encodes during working memory task is still a question that lies at the heart of cognitive neuroscience. The aim of this study is to investigate neural ensemble coding mechanism via average firing rate during working memory task. Neural population activity was measured simultaneously from multiple electrodes placed in prefrontal cortex while rats were performing a working memory task in Y-maze. Then the original data was filtered by a high-pass filtering, spike detection and spike sorting, spatio-temporal trains of neural population were ultimately obtained. Then, the average firing rates were computed in a selected window (500ms) with a moving step (125ms). The results showed that the average firing rate were higher during workinig memory task, along with obvious ensemble activity. Conclusion: The results indicate that the working memory information is encoded with neural ensemble activity.


2018 ◽  
Author(s):  
Michael J. Siniscalchi ◽  
Hongli Wang ◽  
Alex C. Kwan

AbstractInstrumental behavior is characterized by the selection of actions based on the degree to which they lead to a desired outcome. However, we lack a detailed understanding of how rewarded actions are reinforced and preferentially implemented. In rodents, the medial frontal cortex is hypothesized to play an important role in this process, based in part on its capacity to encode chosen actions and their outcomes. We therefore asked how neural representations of choice and outcome might interact to facilitate instrumental behavior. To investigate this question, we imaged neural ensemble activity in layer 2/3 of the secondary motor region (M2) while mice engaged in a two-choice auditory discrimination task with probabilistic outcomes. Correct choices could result in one of three reward amounts (single-, double-, or omitted-reward), which allowed us to measure neural and behavioral effects of reward magnitude, as well as its categorical presence or absence. Single-unit and population decoding analyses revealed a consistent influence of outcome on choice signals in M2. Specifically, rewarded choices were more robustly encoded relative to unrewarded choices, with little dependence on the exact magnitude of reinforcement. Our results provide insight into the integration of past choices and outcomes in the rodent brain during instrumental behavior.


1997 ◽  
Vol 78 (1) ◽  
pp. 506-510 ◽  
Author(s):  
Asif A. Ghazanfar ◽  
Miguel A. L. Nicolelis

Ghazanfar, Asif A. and Miguel A. L. Nicolelis. Nonlinear processing of tactile information in the thalamocortical loop. J. Neurophysiol. 78: 506–510, 1997. Rats explore tangible objects in a manner such that, at any given moment in time, multiple facial whiskers simultaneously contact the surface of the object. Although both thalamic and cortical neurons responsible for processing such tactile information have large, multiwhisker receptive fields, it remains unclear what kinds of computations can be carried out by these neuronal populations when behaviorally relevant multiwhisker stimuli are used. By simultaneously recording the activity of up to 78 cortical and thalamic neurons per animal, we observed that the magnitude of sensory responses and the spatial spread of ensemble activity increased in a nonlinear fashion according to the extent and spatial orientation of the multiwhisker stimuli. Supralinear responses were seen more frequently with vertically than with horizontally oriented stimuli. These data suggest that thalamocortical interactions in the rat somatosensory system can generate complex spatial transformations of multiwhisker stimuli that go beyond the classic inhibitory interactions previously observed.


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