Abstract
Extracellular recordings in medial entorhinal cortex have revealed the existence of spatially-modulated firing patterns, which are thought to contribute to a cognitive map of external space. Previous work indicated that during exploration of novel environments, spiking activity in deep entorhinal layers is much sparser than in superficial layers. In the present report, we ask whether this laminar activity profile is a consequence of environmental novelty. We report on a large dataset of juxtacellularly-recorded neurons (n = 70) whose spiking activity was monitored while rats explored either a novel or a familiar environment, or both within the same session. Irrespective of previous knowledge of the environment, deep layer activity was very low during exploration (median firing rate 0.4 Hz for non-silent cells), with a large fraction of silent cells (n = 19 of a total 37), while superficial layer activity was several times higher (median firing rate 2.4 Hz; n = 33). The persistence of laminar differences in firing activity both under environmental novelty and familiarity, and even in head-restrained stationary animals, suggests that sparse coding might be a constitutive feature of deep entorhinal layers.
Highlights
The medial entorhinal cortex (MEC) is a key structure involved in processing of spatial information (Fyhn et al, 2004; Hafting et al, 2005; Derdikman and Moser, 2010)
Juxtacellular recordings in freely-moving animals were obtained according to previously published procedures (Burgalossi et al, 2011; Herfst et al, 2012)
To test whether the low firing activity in deep layers was attributable to the novelty of the environment, we performed nine additional juxtacellular recordings from rats which were habituated to the same O-maze prior to the recording session
Summary
The medial entorhinal cortex (MEC) is a key structure involved in processing of spatial information (Fyhn et al, 2004; Hafting et al, 2005; Derdikman and Moser, 2010). Superficial (L2-3) and deep layers (L5-6) of the MEC show clear differences in anatomical connectivity, as well as intrinsic and functional neuronal properties (Sargolini et al, 2006; Canto and Witter, 2012). In a recent study (Burgalossi et al, 2011), we employed the juxtacellular recording method (Pinault, 1996) to sample individual MEC neurons in behaving animals. Sampling of individual neurons by juxtacellular method revealed strong laminar differences in firing rates in animals exploring novel environments: deep layer neurons displayed much lower rates (all below 1 Hz, with nearly half of them silent) than superficially recorded cells (Burgalossi et al, 2011). While layer differences might be expected due to the marked differences in anatomical connectivity and intrinsic neuronal properties, the reason for the reported low rates in deep layers remains unclear
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