, 2009a and de Almeida et al., 2009b). This mechanism would be expected

to amplify subtle differences between input patterns, which would generate, for example, pattern separation. Furthermore, this mechanism would amplify small differences in peaks of grid cell firing, resulting in a conversion from grid-to-place codes. Thus, the oscillatory structure of EPSCs and IPSCs may represent a framework for both pattern separation and grid-to-place code conversion in the dentate gyrus. The firing of hippocampal GCs in vivo previously was controversial. Early studies indicated high-frequency activity CH5424802 ic50 of GCs in the center of place fields (Jung and McNaughton, 1993, Skaggs et al., 1996 and Leutgeb et al., 2007) and during working memory tasks (Wiebe and Stäubli, 1999). In contrast, more recent work indicated that GCs in vivo are largely silent (Alme et al.,

2010). Our results demonstrate that morphologically identified GCs in awake rats fire at low frequency. However, when GCs generate spikes, they preferentially fire in bursts. Both the negative resting potential and the coexistence of firing and silent GCs are consistent with the idea that bursting does not represent an artifact of WC recording or a pathophysiological event. Thus, mature GCs in awake animals may primarily use a sparse burst coding mechanism for 3-Methyladenine cost representation of information (reviewed by Lisman, 1997). Low-frequency bursting activity has major implications for GC output via the mossy fiber Rebamipide system. In combination, the low frequency of spiking and the high proportion of bursts will maximize facilitation at hippocampal

mossy fiber synapses, the sole output synapses from dentate gyrus GCs (Salin et al., 1996, Toth et al., 2000 and Henze et al., 2002). Together with previous results, our findings suggest that two highly nonlinear steps in series govern signal flow from the dentate gyrus to the CA3 region. In the first step, pattern separation promoted by gamma oscillations (de Almeida et al., 2009a and de Almeida et al., 2009b) extracts the differences between input patterns. In the second step, burst amplification of mossy fiber transmission generates a highly efficient output onto CA3 pyramidal neurons. This enchainment of two highly nonlinear processes ensures that novel information is selectively relayed to the CA3 region, where it can be used to initiate the efficient storage in CA3–CA3 pyramidal neuron synapses via heterosynaptic potentiation (Kobayashi and Poo, 2004 and Bischofberger et al., 2006). Patch-clamp recordings were made from morphologically identified mature dentate gyrus GCs of the dorsal hippocampus in vivo, using 28- ± 1-day-old Wistar rats of either sex. Experiments followed previous protocols (Margrie et al., 2002, Lee et al., 2006 and Lee et al.