Abstract
Transient and sustained inhibitory synaptic inputs to on-centre, off-centre, and on-off ganglion cells in the mudpuppy retina were studied using intracellular recording in the superfused eye-cup preparation. When chemical transmission was blocked with 4 mM-Co2+, application of either glycine or gamma-aminobutyric acid (GABA) caused a hyperpolarization and conductance increase in all ganglion cells. For both amino acids, the responses were dose dependent in the range 0.05-10 mM, with a half-maximal response at about 0.7 mM. Glycine and GABA sensitivities were very similar in all three types of ganglion cells. The response to applied glycine was selectively antagonized by 10(-5) M-strychnine and the response to applied GABA was selectively antagonized by 10(-5) M-picrotoxin. In all ganglion cells, 10(-5) M-strychnine eliminated the transient inhibitory events which occur at the onset and termination of a light stimulus. The block of transient inhibition was associated with a relative depolarization of membrane potential and decrease in conductance at these times. Strychnine had no effect on membrane potential or conductance in darkness or during sustained inhibitory responses to light. Picrotoxin (10(-5) M) did not block transient inhibitory events in any ganglion cells, but did affect other components of their responses. The results suggest that in all three classes of ganglion cells transient inhibition, but not sustained inhibition, may be mediated by glycine or a closely related substance.
MeSH Terms
Animals
Dose-Response Relationship, Drug
Electric Conductivity
GABA Antagonists
Glycine/antagonists & inhibitors,pharmacology
In Vitro Techniques
Membrane Potentials/drug effects
Necturus
Neural Inhibition/drug effects
Picrotoxin/pharmacology
Retina/physiology
Retinal Ganglion Cells/drug effects,physiology
Strychnine/pharmacology
gamma-Aminobutyric Acid/pharmacology
Chemicals
GABA Antagonists
Picrotoxin
gamma-Aminobutyric Acid
Strychnine
Glycine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Belgum J H
Dvorak D R
McReynolds J S
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