No abstract

Seven Japanese monkeys (Macaca fuscata) were used to investigate the fiber pathways of the optic nerve. Optic nerve fibers and retinal ganglion cells were retrogradely labeled by iontophoretic injections of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) into electrophysiologically defined positions of the lateral geniculate nucleus (LGN). By gross anatomical observation, the optic nerve usually had one distinct bend, which flexed dorsally 3-4 mm from the eyeball, and occasionally another ventrally directed bend was found just behind the eyeball. In the optic nerve head, fibers from the various retinal areas were arranged in a wedge according to the fiber trajectory on the retinal surface. For about a 3 mm distance from the disc, fibers rapidly spread out radially. Subsequently, rather than scattering dorsoventrally, they progressed to the chiasm with a gradual increase in the degree of mediolateral (nasotemporal) scatter. The degree of the scatter was different depending on the retinal site from which the axons originated. Fibers from the peripheral retina spread out widely for a few millimeters behind the eyeball. Thereafter the scatter was rather limited until the chiasm. On the other hand, the scatter of fibers from the foveal and parafoveal areas progressed gradually through the nerve. The present study also suggests that the difference in scatter depends on the types of cells of origin. Fibers from large ganglion cells displayed more extensive scatter than fibers from medium-sized cells. In spite of the extensive scatter of fibers, two clear segregations were found; one was a dorsoventral segregation, which was displayed by both central and peripheral retinal fibers, and the other was a center-peripheral segregation in which the fibers from the nasal central (papillomacular) retina were located almost exclusively in the central part of the optic nerve surrounded by peripheral retinal fibers. However, the temporal central retinal fibers were located in the lateral periphery of the nerve, and they overlapped significantly with fibers from the temporal peripheral retina. Furthermore, a broad intermingling was found between nasal and temporal peripheral retinal fibers owing to their mediolateral scatter. Thus, the present findings based on more precise anatomical techniques indicate that the classical notion of the retinal quadrant topography in the monkey optic nerve probably is suspect. In addition, the "rotation" of the fiber arrangement was not demonstrated.

This study investigated the organization of cells in the ganglion cell layer (GCL) using Nissl staining, retrograde cell degeneration with axotomy of the optic nerve, and retrograde cell labeling by injections of horseradish peroxidase (HRP) into the optic nerve of chicks (posthatching day 1 and 8, P-1 and P-8). The total number of cells in the GCL was 6.1 × 10⁶ (P-1) and 4.9 × 10⁶ (P-8), and the cell density was 14,300 cells/mm² (P-1) and 10,400 cells/ mm² (P-8) on average. Two high-density areas, the central area (CA) and the dorsal area (DA), were observed in the central and dorsal retinas in both P-1 (22,000 cells/mm² in CA, 19,000 cells/mm² in DA) and P-8 chicks (19,000 cells/mm² in CA, 12,800 cells/mm² in DA). The cell densities in the temporal periphery (TP) and the nasal (NP) peripheral retinas were 7,800 cells/mm² and 12,500 cells/mm², respectively, in P-1 and 5,000 cells/ mm² and 8,000 cells/mm², respectively, in P-8 chicks. The cell density in the temporal periphery was 35% (P-8) lower than in the nasal periphery in both P-1 and P-8 chicks. Thirty percent (1.9 × 10⁶ cells in P-1) of the total cells in the GCL were resistant to axotomy of the optic nerve. The distribution of the axotomy-resistant cells showed two high-density areas in the central and dorsal retinas, corresponding to the CA (5,800 cells/mm²) and the DA (3,200 cells/mm²). These cells also exhibited a center-peripheral increase (2,200 cells/mm² in the TP) in P-1 chicks, but the high-density area was not found in the dorsal retina of P-8 chicks. From these data and the HRP study, the number of presumptive ganglion cells in P-8 chicks was estimated to be 4 × 10⁶ (8,600 cells/mm² on average), and the density in each area was 13,500 (CA), 10,200 (DA), and 4,300 (TP) cells/mm². The peripheral/ center ratios of the density of ganglion cells were significantly different along the nasotemporal and dorsoventral axes. The density of ganglion cells decreased more rapidly toward the temporal periphery (TP/CA ratio: 0.47 in P-1 and 0.32 in P-8) than toward the nasal periphery (NP/CA ratio: 0.67 in P-1 and 0.52 in P-8). In contrast, there was no significant difference in the peripheral/center ratios between the dorsal retina (DP/CA ratio: 0.6 in P-1 and 0.56 in P-8) and ventral retina (VP/CA ratio: 0.58 in P-1 and 0.51 in P-8). A small peak in the density of the presumptive ganglion cells was detected in the dorsal retina of both P-1 chicks (10,800 cells/mm²) and P-8 chicks (10,200 cells/mm²). The HRP-labeled cells were small in the CA (M ± SD: 35.7 ± 9.1 μm²) and DA (40.0 ± 11.3 μm²), and their sizes increased toward the periphery (63.4 ± 29.7 μm² in the TP) accompanied by a decrease in the cell density. However, the axotomy-resistant cells did not significantly increase in size toward the pe...

No abstract