Synthesis of nitric oxide (NO) occurs downstream from activation of NMDA re
ceptors and NO acts as a retrograde messenger, influencing the refinement a
nd stabilization of coactive afferent terminals. Cells and neuropil in the
rat superior colliculus (SC) and lateral geniculate body (LGB) show intense
, developmentally regulated activity for NO synthase (NOS). To study the ro
le of NO in the development of retinogeniculate and retinotectal axon arbor
s, we examined primary visual projections of rats that had received daily i
.p. injections of L-NoArg (an NOS inhibitor) for 4-6 weeks starting from po
stnatal day 0. Retinal fibers labeled by intraocular injection of the B sub
unit of cholera toxin were revealed immunohistochemically and the density o
f fibers in the superficial SC and in the dorsal LGB was measured by comput
erized image analysis. Single retinocollicular terminal arbors were reconst
ructed at the computer (Neurolucida).
Treated rats showed significant alterations in ipsilateral retinotectal pro
jections, in the mediolateral and anteroposterior axes: there was an increa
se in the density of fibers entering the SC, in branch length, and in numbe
rs of boutons on retinotectal arbors in the treated group. Ipsilaterally pr
ojecting retinal axons also showed an increase in density and distribution
in the dorsal nucleus of the LGB. If animals were allowed to survive for se
veral months after stopping treatment, similar changes were also noted, but
these were much less striking.
Our results suggest that, in the mammalian visual system, NO released from
target neurons in the SC and LGB serves as a retrograde signal which feeds
back on retinal afferents, influencing their growth.