We investigated the role of 5HT3 receptors in the mammalian retina usi
ng electrophysiological techniques to monitor ganglion cell activity.
Activation of 5HT3 receptors with the selective agonist 1-phenylbiguan
ide (PBG) increased the ON responses of ON-center ganglion cells, whil
e decreasing the OFF responses of OFF-center cells. The application of
a selective 5HT3 antagonist had a reciprocal effect, namely it reduce
d the center response in ON-center cells and concomitantly increased t
he center responses in OFF-center cells. Since putative serotoninergic
amacrine cells in the retina are connected specifically to the rod bi
polar cell, these agents most likely affect the rod bipolar terminal.
These data, together with previous studies, suggest that both 5HT2 and
5HT3 receptors mediate an excitatory influence which serves to facili
tate the output from rod bipolar cells, the former via a phosphatidyl
inositol second-messenger system, and the latter via a direct ion chan
nel.