The behavior of mossy cells of the rat dentate gyrus during theta oscillationsin vivo
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2019, Cell ReportsCitation Excerpt :Notably, mice treated with iDREADDs exhibited a selective increase in theta power before pilocarpine injection (Figure 1G2). These results are relevant to the finding that MCs can discharge at theta rhythm (Henze and Buzsáki, 2007; Soltesz et al., 1993). They are also consistent with the report that MC ablation led to increased theta power, which was explained by a reduction in MC→GABAergic neuron→GC inhibition (Jinde et al., 2012).
Function of local circuits in the hippocampal dentate gyrus-CA3 system
2019, Neuroscience ResearchPhysiological Properties and Behavioral Correlates of Hippocampal Granule Cells and Mossy Cells
2017, NeuronCitation Excerpt :However, this histologic classification is insufficient to differentiate dentate gyrus cell types, because mossy cells and large interneurons in the subgranular layers can generate large amplitude extracellular spikes that can be effectively volume-conducted to a recording electrode in the granule cell layer (Henze and Buzsáki, 2007). This reliance on electrode placement for classification of recorded cells has led to large variability of neurophysiologic features attributed to granule cells (as fast firing: Bland et al., 1980; Buzsáki et al., 1983; Rose et al., 1983; Leutgeb et al., 2007 or slow firing: Mizumori et al., 1989; Jung and McNaughton, 1993; Gothard et al., 2001; Nitz and McNaughton, 2004; Neunuebel and Knierim, 2012, 2014) and to a lack of reliable data about mossy cell firing patterns and behavioral correlates (Henze and Buzsáki, 2007; Jinde et al., 2012; Neunuebel and Knierim, 2012, 2014; Soltesz et al., 1993). To understand how granule cells and mossy cells contribute to the postulated computation of the dentate gyrus, it is necessary to develop parameters that allow their unequivocal separation in extracellular recordings.