Light-dark periodicity and luminance play important roles in regulating sle
ep-wake cycles. We recently identified a discrete cluster of sleep-active c
ells in the ventrolateral preoptic nucleus that we hypothesize plays a cent
ral role in sleep regulation. These ventrolateral preoptic nucleus neurons
are GABAergic and galaninergic and innervate the monoaminergic cell groups
that contribute to the ascending arousal system. To determine whether there
are retinal inputs to sleep-active ventrolateral preoptic nucleus neurons,
we injected 5 mu l of 1% cholera toxin B subunit into one eye in a series
of rats. We found anterogradely labeled axons in the ventrolateral preoptic
nucleus bilaterally, with a contralateral predominance. Using Fos to ident
ify sleep-active neurons, we found that the cholera toxin B subunit-labeled
retinal fibers gave rise to terminals that were distributed among the Fos-
positive, sleep-active ventrolateral preoptic nucleus neurons. Combining ch
olera toxin B subunit staining with galanin immunoreactivity, we found that
the retinal terminals formed appositions with the cell bodies and proximal
dendrites of galaninergic ventrolateral preoptic nucleus neurons. Followin
g Fluorogold injection into the ventrolateral preoptic nucleus region. we f
ound retrogradely labeled neurons in the superior part of the peripheral re
tina contralateral to the injection site and in the superior temporal quadr
ant of the peripheral retina ipsilateral to the injection site. The size of
labeled retinal ganglion cells suggested that they belonged to the type II
I or W type, which provide luminance input, e.g., to the suprachiasmatic nu
cleus. The retinal projection to the ventrolateral preoptic nucleus may pro
vide an anatomical substrate by which luminance levels may directly influen
ce sleep. (C) 1999 IBRO. Published by Elsevier Science Ltd.