Light decrements are mediated by two distinct groups of rod pathways
in the dark-adapted retina that can be differentiated on the basis of
their sensitivity to the glutamate agonist DL-2-amino-phosphonobutyric
(APB). By means of the APB sensitive pathway, rods transmit light
decrements via rod bipolar cells to AII amacrine cells, then to
Off cone bipolar cells, which in turn innervate the dendrites of Off
ganglion cells. APB hyperpolarizes rod bipolar cells, thus blocking this
rod pathway. With APB insensitive pathways, rods either directly synapse
onto Off cone bipolar cells, or rods pass light decrement signal to cones
by gap junctions. In the present study, whole-cell patch-clamp recordings
were made from ganglion cells in the dark-adapted mouse retina to
investigate the functional properties of APB sensitive and insensitive rod
pathways. The results revealed several clear-cut differences between the
APB sensitive and APB insensitive rod pathways. The latency of Off
responses to a flashing spot of light was significantly shorter for the
APB insensitive pathways than those for the APB sensitive pathway.
Moreover, Off responses of the APB insensitive pathways were found to be
capable of following substantially higher stimulus frequencies. Nitric
oxide was found to selectively block Off responses in the APB sensitive
rod pathway. Collectively, these results provide evidence that the APB
sensitive and insensitive rod pathways can convey different types of
information signaling light decrements in the dark-adapted retina.