GABA Receptors of Bipolar Cells From the Skate Retina: Actions of Zinc on GABA-Mediated Membrane Currents

Author:

Qian Haohua12,Li Lihong13,Chappell Richard L.13,Ripps Harris14

Affiliation:

1. The Marine Biological Laboratories, Woods Hole, Massachusetts 02543;

2. Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138;

3. Department of Biological Sciences, Hunter College and Graduate School, City University of New York, New York 10021

4. Department of Ophthalmology and Visual Sciences, University of Illinois College of Medicine, Chicago, Illinois 60612; and

Abstract

Qian, Haohua, Lihong Li, Richard L. Chappell, and Harris Ripps. GABA receptors of bipolar cells from the skate retina: actions of zinc on GABA-mediated membrane currents. J. Neurophysiol. 78: 2402–2412, 1997. γ-Aminobutyric acid (GABA)–induced currents were recorded from isolated bipolar cells of the skate retina using perforated patch-clamp methodology. Pharmacological analysis of the responses, using selective agonists and antagonists of the major classes of GABA receptor, revealed the presence of both GABAA and GABAC receptors at both the dendrites and axon terminals of the bipolar cells. The two receptor types showed very different reactions to zinc, a divalent metallic cation that was detected in the synaptic terminal region of skate photoreceptors. Currents mediated by the activation of GABAC receptors were down-regulated by zinc, a feature that is typical of the action of zinc on GABAC receptors. On the other hand, the effects of zinc on GABAA receptor–mediated activity was highly dependent on zinc concentration. Unlike theGABAA receptors on other neurons, responses mediated by activation of the GABAA receptor of skate bipolar cells were significantly enhanced by zinc concentrations in the range of 0.1–100 μM; at higher concentrations of zinc (>100 μM), response amplitudes were suppressed below control levels. The enhancement of GABAA receptor activity on skate bipolar cells showed little voltage dependence, suggesting that zinc is acting on the extracellular domain of the GABAA receptor. In the presence of 10 μM zinc, the dose-response curve for 4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol (THIP; a GABAA agonist that suppresses GABAC-activated currents) was shifted to the left of the curve obtained in the absence of zinc, but without a significant change in the response maximum. This finding indicates that the enhancing effect of zinc is due primarily to its ability to increase the sensitivity of the GABAA receptor. The novel enhancement of neuronal GABAA receptor activity by zinc, observed previously in the GABAA-mediated responses of skate Müller (glial) cells, may reflect the presence of a unique subtype of GABAA receptor on the bipolar and Müller cells of the skate retina.

Publisher

American Physiological Society

Subject

Physiology,General Neuroscience

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