Comparative distribution of 3H‐GABA uptake and GAD immunoreactivity in goldfish retinal amacrine cells: A double‐label analysis

Abstract

The comparative distribution of ³H‐GABA uptake and glutamic acid decarboxylase immunoreactivity (GAD‐ER) in amacrine cells of goldfish retina was studied simultaneously by using a combined autoradiographic/immunocytochemical technique in order to determine the degree of colocalization of these two markers of GABAergic neurons; ³H‐GABA was taken up most intensely by large pyriform Ab amacrine cells (3% of inner nuclear layer (INL) somata), and less intensely by smaller, polyform amacrine cells (12% of INL somata), cell bodies in the ganglion cell layer (one‐half as common as Ab cells), and cell bodies in the inner plexiform layer (very rare). GAD‐IR was observed in 25% of amacrine cells in the INL, the vast majority of which were polyform in shape, and cell bodies in the ganglion cell layer. Twice as many cells were labeled for GAD‐IR as for ³H‐GABA uptake. Of the cells that took up ³H‐GABA, colocalization of ³H‐GABA uptake and GAD‐IR was observed in 90% of the polyform amacrine cells, 80% of the cells in the ganglion cell layer, and none of the pyriform Ab amacrine cells or cells in the inner plexiform layer. We suggest that the polyform cells compose the major population of GABAergic amacrine cells in the goldfish retina, rather than the pyriform Ab cells. GABAergic displaced amacrine cells or ganglion cells are also indicated by our data. The implications of these data with regard to the physiology of the goldfish retina are discussed as well.