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Volume 17, Number 16, Issue of August 15, 1997 pp. 6075-6085
Copyright ©1997 Society for Neuroscience

GABAergic and glycinergic IPSCs in Ganglion Cells of Rat Retinal Slices

Received Feb. 26, 1997; revised May 27, 1997; accepted June 2, 1997.

Dario A. Protti1, Hersch M. Gerschenfeld2, and Isabel Llano1

1 Arbeitsgruppe Zelluläre Neurobiologie, Max-Planck-Institut für biophysikalische Chemie, 37070 Göttingen, Germany, and 2 Laboratoire de Neurobiologie, Ecole Normale Supérieure, 75005 Paris, France

GABAergic and glycinergic IPSCs were studied in identified retinal ganglion cells (RGCs) of light-adapted rat retinal slices, using whole-cell recording techniques. GABAergic IPSCs were blocked specifically by SR95531 (3 µM) and bicuculline (3 µM) and glycinergic IPSCs by strychnine (0.3 µM). From 37 RGCs studied, 25 showed exclusively GABAergic IPSCs, 6 presented only glycinergic IPSCs, and 6 showed both. This distribution may result from differences in amacrine cells input rather than from receptor heterogeneity, because both GABA and glycine elicited Cl--selective currents in all RGCs tested. TTX markedly reduced GABAergic IPSCs frequency, whereas glycinergic IPSCs were unaffected. Ca2+-free media, with or without high Mg2+, blocked TTX-resistant GABAergic and glycinergic IPSCs. These results suggest that GABAergic IPSCs in RGCs can be elicited either by Na+-dependent action potentials or by local Ca2+ influx in medium or large dendritic field GABAergic amacrine cells, whereas glycinergic IPSCs are generated by action potential-independent Ca2+ influx in narrow field glycinergic amacrine cells. Both types of IPSCs had fast rise times and biexponential decays, but glycinergic IPSC decay was significantly slower than that of GABAergic IPSCs. An elementary conductance of 54 pS for the glycine-gated channels was estimated from single-channel events, clearly detected in the falling phase of glycinergic IPSCs, and from responses to exogenous glycine.

Key words: synaptic currents; GABA; glycine; retina; patch-clamp; neurotransmitter receptors




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