ABSTRACT. Four cell types including the bipolar, amacrine, horizontal and Muller cells were investigated quantitatively in the inner nuclear layer of the retina in the horse. Cells were identified on the basis of the morphology and distribution of processes leaving from their somata, cytological features and positional features. The average percentages of the above 4 cell types were 44%, 24%, 1% and 29%, respectively. The average total cell densities in the inner nuclear layer in the visual streak, the nasal and temporal regions, the dorsal and ventral regions of the retina were also estimated. It is expected that the results of this study will supply the basic data for further study of the neural circuits in the horse retina. KEY WORDS: cell type, equine, inner nuclear layer.J. Vet. Med. Sci. 64(9): 847-849, 2002 The inner nuclear layer of the retina contains 4 cell types: the bipolar, amacrine, horizontal and Müller cells. To understand the functions of the cells and neural circuits of the retina completely, the cellular composition in the inner nuclear layer must be known. In the present study, we identified each cell in the inner nuclear layer of the horse retina using a method of serial reconstruction [5]. The percentage and density of each cell type were calculated. On the other hand, in a previous study on the retinal ganglion cells of the horse, we divided the retina into 5 regions according to ganglion cell densities and retinal locations as follows: visual streak, and nasal, temporal, dorsal and ventral regions [1]. The other purpose of the study was to compare cell distributions in the inner nuclear layer among 5 regions.Three eyeballs (L1, L2, R3) from different adult horses (Thoroughbred) were used in the present study. After the horse was killed in a local slaughterhouse, the eyeballs were enucleated quickly and orientations of eyeballs were marked with a marking pen. Eyeballs were hemisected and the retinal blocks with a width of 1 mm and a length of 2-3 mm were sampled from 5 regions of the retina, respectively. The blocks were immersed in 2.5% phosphate buffered glutaraldehyde and 1% paraformaldehyde for 3-4 hr at 4°C, postfixed in 1% osmium tetroxide for 2 hr, dehydrated and embedded in Epok 812. From every retinal block, 16-20 consecutive thin vertical sections were cut at 1 µm with an ultramicrotome (ULTRACUT N, Reichert-Jung Optische Werke AG, Vienna, Austria), mounted onto uncoated glass slides and stained with 0.3% toluidine blue. All consecutive sections were observed under a light microscope and micrographs were taken at 950× using a 100 × oil immersion objective.Cells in the inner nuclear layer of the retina were identified on the basis of the morphology and distribution of processes leaving from their somata [5], cytological features (dark or pale matrix etc.) and positional features (at the outer or inner border of the inner nuclear layer). The bipolar cell injected dendrites from the scleral side of the cell body (Fig. 1B) toward the outer plexiform layer, and extended an axon fr...