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The Journal of Neuroscience, May 1, 1998, 18(9):3451-3459
Response to Change Is Facilitated by a Three-Neuron Disinhibitory
Pathway in the Tiger Salamander Retina
Botond
Roska,
Erik
Nemeth, and
Frank S.
Werblin
Division of Neurobiology, Department of Molecular and Cell Biology,
University of California at Berkeley, Berkeley, California 94720
Most retinal ganglion cells respond only transiently, for ~150
msec at the onset and termination of a light flash. The responses are
transient because it has been shown that bipolar-to-ganglion cell
transmission is truncated after 150 msec by a feedback inhibition to
bipolar cell terminals. The feedback inhibition itself must be delayed
by ~150 msec to allow the initial bipolar-ganglion cell
transmission. This study identifies a three-component serial synaptic
pathway from glycinergic amacrine cells to GABAergic amacrine cells to
bipolar cell terminals as one source of this delay. We used perforated
and whole-cell patch-clamp recordings to measure the timing of light
responses in amacrine, bipolar, and ganglion cells under control and
glycine and GABA receptor-blocked conditions. Our results suggest that,
after a light flash, a population of glycinergic amacrine cells
responds first, inhibiting a population of GABAergic amacrine cells for
~150 msec. The GABAergic amacrine cells feed back to bipolar
terminals, but only after the 150 msec delay, allowing the bipolar
terminals to excite ganglion cells for the first 150 msec. Blocking the
glycinergic amacrine cell activity with strychnine allows the GABAergic
system to become active earlier. GABAergic amacrine cells then inhibit
release from bipolar cells earlier. Under these conditions, the
ganglion cell response to change would be decreased.
Key words:
amacrine cell; glycine; GABA; disinhibition; reciprocal
inhibition; retina; patch clamp
Copyright © 1998 Society for Neuroscience 0270-6474/98/1893451-09$05.00/0
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