The cellular generation and spatial distribution of gamma frequency (4
0-100 Hz) activity was examined in the hippocampus of the awake rat. F
ield potentials and unit activity were recorded by multiple site silic
on probes (5- and 16-site shanks) and wire electrode arrays. Gamma wav
es were highly coherent along the long axis of the dentate hilus, but
average coherence decreased rapidly in the CA3 and CA1 directions. Ana
lysis of short epochs revealed large fluctuations in coherence values
between the dentate and CA1 gamma waves, Current source density analys
is revealed large sinks and sources in the dentate gyrus with spatial
distribution similar to the dipoles evoked by stimulation of the perfo
rant path, The frequency changes of gamma and theta waves positively c
orrelated (40-100 Hz and 5-10 Hz, respectively), Putative interneurons
in the dentate gyrus discharged at gamma frequency and were phase-loc
ked to the ascending part of the gamma waves recorded from the hilus,
Following bilateral lesion of the entorhinal cortex the power and freq
uency of hilar gamma activity significantly decreased or disappeared.
Instead, a large amplitude but slower gamma pattern (25-50 Hz) emerged
in the CA3-CA1 network, We suggest that gamma oscillation emerges fro
m an interaction between intrinsic oscillatory properties of interneur
ons and the network properties of the dentate gyrus. We also hypothesi
ze that under physiological conditions the hilar gamma oscillation may
be entrained by the entorhinal rhythm and that gamma oscillation in t
he CA3-CA1 circuitry is suppressed by either the hilar region or the e
ntorhinal cortex.