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Phencyclidine Discoordinates Hippocampal Network Activity But Not Place Fields.

Hsin-Yi Kao, Dino Dvořák, Eunhye Park, Jana Kenney, Eduard Kelemen, André A Fenton

The Journal of neuroscience : the official journal of the Society for Neuroscience December 6, 2017 DOI: 10.1523/jneurosci.0630-17.2017 via PubMed

Summary

AI-generated from the abstract

The psychotomimetic drug phencyclidine (PCP) impairs a learned hippocampus-dependent place avoidance behavior in rats, even when injected directly into the dorsal hippocampus. PCP increases 60-100 Hz gamma oscillations in hippocampal CA1, and these increases correlate with cognitive impairment. PCP disrupts the coordination between theta-modulated medium-frequency and slow gamma oscillations, and it disrupts the subsecond temporal organization of discharge among place cells, causing ensemble representations of a familiar space to cease resembling pre-PCP representations despite preserved place fields. These findings indicate that PCP-induced cognitive impairments arise from neural discoordination, specifically excitation-inhibition discoordination, rather than from disruption of place fields themselves.

Study at a glance

Characteristics Experimental study Peer reviewed
Population Rats
Intervention Phencyclidine (PCP)
Dose 5 mg/kg, i.p.
Keywords Nmda antagonist Gamma Neural discoordination Oscillations Place cell
Key finding PCP impairs cognitive behavior by disrupting the temporal coordination of hippocampal neural discharge on theta and gamma timescales, while preserving place cell firing fields.

Abstract

We used the psychotomimetic phencyclidine (PCP) to investigate the relationships among cognitive behavior, coordinated neural network function, and information processing within the hippocampus place cell system. We report in rats that PCP (5 mg/kg, i.p.) impairs a well learned, hippocampus-dependent place avoidance behavior in rats that requires cognitive control even when PCP is injected directly into dorsal hippocampus. PCP increases 60-100 Hz medium-freguency gamma oscillations in hippocampus CA1 and these increases correlate with the cognitive impairment caused by systemic PCP administration. PCP discoordinates theta-modulated medium-frequency and slow gamma oscillations in CA1 LFPs such that medium-frequency gamma oscillations become more theta-organized than slow gamma oscillations. CA1 place cell firing fields are preserved under PCP, but the drug discoordinates the subsecond temporal organization of discharge among place cells. This discoordination causes place cell ensemble representations of a familiar space to cease resembling pre-PCP representations despite preserved place fields. These findings point to the cognitive impairments caused by PCP arising from neural discoordination. PCP disrupts the timing of discharge with respect to the subsecond timescales of theta and gamma oscillations in the LFP. Because these oscillations arise from local inhibitory synaptic activity, these findings point to excitation-inhibition discoordination as the root of PCP-induced cognitive impairment.SIGNIFICANCE STATEMENT Hippocampal neural discharge is temporally coordinated on timescales of theta and gamma oscillations in the LFP and the discharge of a subset of pyramidal neurons called "place cells" is spatially organized such that discharge is restricted to locations called a cell's "place field." Because this temporal coordination and spatial discharge organization is thought to represent spatial knowledge, we used the psychotomimetic phencyclidine (PCP) to disrupt cognitive behavior and assess the importance of neural coordination and place fields for spatial cognition. PCP impaired the judicious use of spatial information and discoordinated hippocampal discharge without disrupting firing fields. These findings dissociate place fields from spatial cognitive behavior and suggest that hippocampus discharge coordination is crucial to spatial cognition.

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