We have examined the spatiotemporal properties of ensemble activity, an evo
ked all-or-none polysynaptic activity in rat neocortical slices. Ensemble a
ctivity occurred in cortical slices bathed in normal artificial cerebrospin
al fluid (ACSF) and was evoked by a single electrical shock either to the w
hite matter or directly to the cortical tissue. This activity was seen in s
lices of somatosensory and auditory cortices; in other cortical areas we ha
ve not been able to evoke it. The activity developed 10 to 250 ms poststimu
lus and lasted 280 +/- 120 ms in local field potential (LFP) recordings. Vo
ltage-sensitive dye imaging showed that this activity was an area of activa
tion 0.8 +/- 0.4 mm wide that propagated slowly (11.4 +/- 6.2 mm/s, n = 60,
6 animals) in the horizontal direction. Due to this propagation, the actua
l duration in the whole tissue may be longer (similar to 400 ms) than that
recorded by a single LFP electrode. Ensemble activity produced a low-amplit
ude optical signal (7-14% of the interictal-like spikes in the same tissue)
, suggesting a moderate net depolarization of the population. These were ve
ry different from hyperexcitable (epileptiform) events in the same tissue t
hat had about 10 times the optical signal amplitude and propagated at 125 /- 24 mm/s (n = 21, 6 animals). On a global spatial scale (similar to0.8 mm
wide in layers II-III) ensemble activity had a smooth waveform in voltage-
sensitive dye signals (population transmembrane potential). On a local scal
e, field potential recordings showed large fluctuations with complex oscill
ations and substantial trial-to-trial variation. This suggests that oscilla
tions in cortical circuits occurred only in small clusters of correlated ne
urons. Ensemble activity was sensitive to the excitation-inhibition balance
of the local network. Antagonists of N-methyl-D-aspartate, alpha -amino-3-
hydroxy-5-methyl-4-isoxazolepropionic acid, and GABAa receptors, and muscar
inic agonists and other modest manipulations such as increasing bath concen
tration of Mg2+ to 2.5-4 mM (normally at 2 mM), or K+ to 5-7 mM (normally 3
mM), all significantly reduced the probability of evoking the activity. Th
e metabotropic glutamate receptor agonist, aminocyclopentane-1,3-dicarboxyl
ic acid, blocked the activity at a low concentration (10-15 muM), while the
antagonist (R,S)-alpha -methyl-4-carboxyphenylglycine had no effect even a
t high concentration (240 muM). Our data suggest that locally organized neu
ronal clusters may play a role in the organization of oscillatory activitie
s in the gamma band and may participate in cortical integration/amplificati
on occurring on a scale of similar to1 mm x 300 ms.