T. Morales et al., Prolactin-releasing peptide is expressed in afferents to the endocrine hypothalamus, but not in neurosecretory neurones, J NEUROENDO, 12(2), 2000, pp. 131-140
Prolactin release from the anterior pituitary is regulated principally by i
nhibitory influences imparted by the tuberoinfundibular dopamine system. St
imulatory control is provided by several hypothalamic, peripheral and local
factors. Recently a new peptide, prolactin releasing peptide (PrRP), showi
ng prolactin-secretagogue effects was discovered, synthesized and found to
be expressed in brain. We have used histochemical and axonal transport meth
ods to characterize the distribution of PrRP mRNA in the rat brain, and to
identify possible pathways through which this factor might be delivered to
the anterior lobe of the pituitary and thereby participate in the regulatio
n of prolactin secretion. Analysis of histochemical preparations indicated
that apart from a small population of cells in a non-neurosecretory portion
of the hypothalamus, PrRP mRNA is expressed exclusively in the caudal part
of the nucleus of the solitary tract and in the caudal ventrolateral medul
la, All medullary PrRP expressing cells could be immunolabeled for tyrosine
hydroxylase, and none were found to stain for glucagon-like peptide-1, ide
ntifying them as comprising subsets of A2 and A1 noradrenergic neurones, re
spectively. Numerous PrRP-expressing cells were retrogradely labelled follo
wing tracer injections in the paraventricular nucleus, while only a handful
were backfilled following intravenous injections of tracer, indicating tha
t this population issues substantial projections to the endocrine hypothala
mus and meager ones to the median eminence and/or posterior pituitary, This
conclusion was supported by the results of experiments in which the antero
grade tracer, biotinylated dextran-amine, was injected into the PrRP cell g
roup in the nucleus of the solitary tract, These findings suggest that PrRP
expressing neurones display a highly restricted distribution, and are in a
position to regulate the output of particular cell types in the endocrine
hypothalamus, Whether and how PrRP might be delivered to the anterior pitui
tary remains to be determined.