M. Moller et al., Innervation of the rat pineal gland by pituitary adenylate cyclase-activating polypeptide (PACAP)-immunoreactive nerve fibres, CELL TIS RE, 296(2), 1999, pp. 247-257
Pituitary adenylate cyclase-activating polypeptide (PACAP)-immunoreactive n
erve fibres were demonstrated in the rat pineal gland. These fibres entered
the pineal gland through the conarian nerve at the distal tip of the gland
. A high density of the fibres was observed in the capsule of the gland, fr
om where the immunoreactive elements penetrated into the pineal perivascula
r spaces and parenchyma. The majority of PACAP-immunoreactive nerve fibres
also contained calcitonin gene-related peptide (CGRP). Some PACAP-immunorea
ctive nerve fibres contained neuropeptide Y (NPY), but only occasionally wa
s PACAP colocalized with vasoactive intestinal peptide (VIP). After removal
of both superior cervical ganglia, a high number of PACAP-containing nerve
fibres were still present in the gland. In the nervous system PACAP is pre
sent in two isoforms, PACAP-38 and PACAP-27. The concentration of PACAP-38
in the superficial pineal gland was determined by radioimmunoassay to be 20
.4 pmol/g tissue at midday and 18.9 pmol/g tissue at midnight. The concentr
ation of PACAP-27 was only about 3% of the concentration of PACAP-38. In su
mmary, this study is the first demonstration of a PACAP-containing innervat
ion of the rat pineal gland. The PACAP concentration in the pineal gland do
es not exhibit a day-night difference. The colocalization of PACAP with cal
citonin gene-related peptide in the pinealopetal nerve fibres indicates tha
t the majority of PACAP-immunoreactive nerve fibres might originate from th
e trigeminal ganglion.