Hippocampal place cells can encode multiple trial-dependent features through rate remapping

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Abstract

The activity of hippocampal pyramidal cells reflects both the current position of the animal and information related to its current behavior. Here we investigated whether single hippocampal neurons can encode several independent features defining trials during a memory task. We also tested whether task-related information is represented by partial remapping of the place cell population or, instead, via firing rate modulation of spatially stable place cells. To address these two questions, the activity of hippocampal neurons was recorded in rats performing a conditional discrimination task on a modified T-maze in which the identity of a food reward guided behavior. When the rat was on the central arm of the maze, the firing rate of pyramidal cells changed depending on two independent factors: (1) the identityofthe food reward given to the animal and (2) the previous locationof the animalonthe maze. Importantly, some pyramidal cells encoded information relative to both factors. This trial-type specific and retrospective coding did not interfere with the spatial representation of the maze: hippocampal cells had stable place fields and their theta-phase precession profiles were unaltered during the task, indicating that trial-related information was encoded via rate remapping. During error trials, encoding of both trial-related information and spatial location was impaired. Finally, we found that pyramidal cells also encode trial-related information via rate remapping during the continuous version of the rewarded alternation task without delays. These results suggest that hippocampal neurons can encode several task-related cognitive aspects via rate remapping. © 2012 the authors.

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APA

Allen, K., Rawlins, J. N. P., Bannerman, D. M., & Csicsvari, J. (2012). Hippocampal place cells can encode multiple trial-dependent features through rate remapping. Journal of Neuroscience, 32(42), 14752–14766. https://doi.org/10.1523/JNEUROSCI.6175-11.2012

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