Cellular bases of hippocampal EEG in the behaving rat.

By György Buzsáki, Leung Lai-Wo S., C. Vanderwolf. 1983

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Citations in the corpus

Hippocampal replay in the awake state: a potential physiological substrate of memory consolidation and retrieval (2011, background): “SWRs are prominent during sleep as well as in the awake state during immobility, consummatory behavior and groomin”
Hippocampal replay of extended experience (2009, neutral): “Such trains have been noted since the first reports of ripples (Buzsáki et al., 1983; O’Keefe and Nadel, 1978; Suzuki and Smith, 1987), but no function has previously been ascribed to this phenomenon.”
Reactivation of Hippocampal Cell Assemblies: Effects of Behavioral State, Experience, and EEG Dynamics (1999, background): “stimulation of the perforant path lead to larger population spikes in CAl during SPWs, suggesting that hippocampal neurons are more excitable during SPWs (Buzsdki et al., 1983).”
New experiences enhance coordinated neural activity in the hippocampus. (2008, unknown): “Ripple or HFE events are indicated by red lines above LFP traces (gray, raw signal; black,band-filtered [150–250 Hz] signal).”
Hippocampal Plasticity across Multiple Days of Exposure to Novel Environments (2004, unknown): “That filtering removed intervals of inactivity when place-specific firing is typically not present (Buzsaki et al., 1983).”
Hippocampal “time cells” bridge the gap in memory for discontiguous events (2011, unknown): “Rats learned the sequences over several training sessions, then performed the task as recordings were taken from multiple tetrode arrays implanted in the pyramidal cell layer of dorsal CA1.”
Distinct hippocampal-cortical memory representations for experiences associated with movement versus immobility (2017, unknown): “Smooth transition between CA1 movement and immobility spatial representations Distinct hippocampal network patterns, the ~8 Hz theta rhythm and N-waves, are associated with periods of movement and immobility, respectively (Buzsáki et al., 1983; Kay et al., 2016).”
Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning (2015, methodology): “In short, SPW-Rs and hippocampal theta oscillations are competing mechanisms (Buzs aki et al., 1983).”
Place cells, grid cells, and the brain's spatial representation system. (2008, background): “Such replay or reactivation is associated with hippocampal sharp waves, which are bursts of synchronous pyramidal-cell activity during slow-wave sleep and awake rest (Buzsáki et al. 1983).”
Natural patterns of activity and long-term synaptic plasticity. (2000, background): “Exploratory learning is associated with characteristic slow rhythmic activity in extracellularly recorded potentials [14].”
High-Frequency Oscillations in the Output Networks of the Hippocampal–Entorhinal Axis of the Freely Behaving Rat (1996, background): “…occurs during exploratory behavior and rapid eye movement sleep and represents a period when hippocampal circuits receive rhythmic input from neurons within the superficial layers of the EC (Mitchell and Ranck, 1980; Buzsáki et al., 1983; Boeijinga and Lopes da Silva, 1988; Stewart et al., 1992).”
Subdivisions in the Multiple GABAergic Innervation of Granule Cells in the Dentate Gyrus of the Rat Hippocampus (1993, background): “of the rhythrmc field potential during theta activity (Andersen, 1980; Buzsaki et al., 1983; Munoz et al., 1990).”