The space-time patterns of activity generated across arrays of retinal neur
ons can provide a sensitive measurement of the effects of neural interactio
ns underlying retinal activity. We measured the excitatory and inhibitory c
omponents associated with these patterns at each cellular level in the reti
na and further dissected inhibitory components pharmacologically. Using per
forated and loose patch recording, we measured the voltages, currents, or s
piking at 91 lateral positions covering similar to 2 mm in response to a fl
ashed 300-mu m-wide bar. First, we showed how the effect of well known late
ral inhibition at the outer retina, mediated by horizontal cells, evolved i
n time to compress the spatial representation of the stimulus bar at ON and
OFF bipolar cell bodies as well as horizontal cells. Second, we showed, fo
r the first time, how GABA(C) receptor mediated amacrine cell feedback to b
ipolar terminals compresses the spatial representation of the stimulus bar
at ON bipolar terminals over time. Third, we showed that a third spatiotemp
oral compression exists at the ganglion cell layer that is mediated by feed
forward amacrine cells via GABA(A) receptors. These three inhibitory mechan
isms, via three different receptor types, appear to compensate for the effe
cts of lateral diffusion of activity attributable to dendritic spread and e
lectrical coupling between retinal neurons. As a consequence, the width of
the final representation at the ganglion cell level approximates the dimens
ions of the original stimulus bar.