It is not clear, though, which signal was the immediate trigger for the CA1 network to generate mutant ripples. Feasible inputs might arise from entorhinal cortex or thalamus (Nakashiba et al., 2009). Collectively, though Schaffer collateral input onto CA1 may be obligatory for the transfer of information involved in memory consolidation, transmission from CA3 to CA1 does not seem to be required for the occurrence of ripple oscillations in CA1 (see also Buzsáki et al., 1992). Ripple-coherent EPSCs in CA1 minislices

are consistent with a second framework to explain their origin. In this scenario, these currents are assumed to be of purely local emergence, resulting from recurrent synaptic input alone (Deuchars and Thomson, 1996). Cellular processes involved in triggering sharp waves are still subject to investigations. Recently, it has been proposed that this website sharp waves in CA3 may be induced by rebound depolarization following strong inhibitory activity (Ellender selleck inhibitor et al., 2010). Sharp-wave-associated excitation arriving from CA3 (Buzsáki, 1986) may consequently trigger sharp waves in CA1, which secondarily

give rise to ripples. The mechanisms responsible for the generation and maintenance of ripples are also a matter of debate. Computational network models provide two possible explanations: First, ripples may reflect the synchronous discharge of pyramidal cells during the replay of memory Vasopressin Receptor sequences (as formulated for CA3 by Leibold and Kempter, 2006). Alternatively, electrical coupling of CA1 principal cell axons may generate oscillations in the ripple frequency range (Traub et al., 1999 and Traub and Bibbig, 2000). This latter hypothesis is supported by experimental reports of spikelets being a consequence of electrical coupling between axons of cortical pyramidal neurons

(Draguhn et al., 1998, Schmitz et al., 2001 and Wang et al., 2010). Along this line, recent work has demonstrated bursts of spikelets in the hippocampus during behavior in vivo (Harvey et al., 2009) and even at ripple frequency (Epsztein et al., 2010). The observed ripple-locked EPSCs could thus correspond to rhythmic output of a gap junction-coupled network of CA1 principal cells. Consistent with this possibility, SWR incidence and cPSC ripple-band power were reduced following application of carbenoxolone (CBX; Figure S9A). However, in agreement with previous work (Tovar et al., 2009), CBX also weakened both excitatory and inhibitory synaptic transmission in our experimental system (Figures S9B and S9C). In light of the poor specificity of CBX, a known limitation of gap junction blockers in general, the hypothesized role of gap junctions in synchronizing the axonal network during ripples remains unsettled and has to be addressed in future work. In summary, we demonstrated coherent excitatory currents in CA1 pyramidal neurons during ripples.