NADPH-diaphorase-positive neurons have been demonstrated in the inner
nuclear layer and ganglion cell layer of the retina of different mamma
lian species, but so far no experiments have been conducted to identif
y whether these cells are amacrine cells and/or retinal ganglion cells
. We attempted to solve this problem by studying the NADPH-diaphorase-
positive neurons in the hamster retina. From the NADPH-diaphorase hist
ochemical reaction, two distinct types of neurons in the hamster retin
a were identified. They were named ND(g) and ND(i) cells. The ND(g) ce
lls were cells with larger somata, ranging from 10 to 21 mu m in diame
ter with a mean of 15.58 mu m (S.D. = 2.59). They were found in the ga
nglion cell layer only. The ND(i) cells were smaller, with the somata
ranging from 7 to 11 mu m and having the mean diameter of 8.77 mu m (S
.D. = 1.24). Most of the ND(i) cells were found in the inner nuclear l
ayer, and only very few could be observed in the inner plexiform layer
. On average, there were 8,033 ND(g) and 5,051 ND(i) cells in the gang
lion cell layer and inner nuclear layer, respectively. Two experiments
were performed to clarify whether any of the NADPH-diaphorase neurons
were retinal ganglion cells. Following unilateral optic nerve section
, which leads to the retrograde degeneration of retinal ganglion cells
, the numbers of both ND(g) and ND(i) cells did not change significant
ly for up to 4 months. In addition, when retinal ganglion cells were p
relabeled retrogradely (horseradish peroxidase or fluorescent microsph
eres) and retinas were then stained for NADPH diaphorase, no double-la
beled neurons were detected. These results indicated that the NADPH-di
aphorase neurons in the hamster retina were the amacrine cells in the
inner nuclear layer and displaced amacrine cells in the ganglion cell
layer. Dendrites of the ND(g) and ND(i) cells were found to stratify i
n sublaminae 1, 3, and 5 of the inner plexiform layer, with a prominen
t staining in the sublamina 5. The possible importance of this arrange
ment in the rod pathway is also discussed. (C) 1994 Wiley-Liss, Inc.