PITUITARY GROWTH HORMONE-RELEASING FACTOR-RECEPTOR EXPRESSION IN NORMAL AND DWARF RATS

Citation
Df. Carmignac et al., PITUITARY GROWTH HORMONE-RELEASING FACTOR-RECEPTOR EXPRESSION IN NORMAL AND DWARF RATS, Neuroendocrinology, 64(3), 1996, pp. 177-185
Citations number
58
Categorie Soggetti
Neurosciences,"Endocrynology & Metabolism
Journal title
ISSN journal
00283835
Volume
64
Issue
3
Year of publication
1996
Pages
177 - 185
Database
ISI
SICI code
0028-3835(1996)64:3<177:PGHFEI>2.0.ZU;2-T
Abstract
Growth hormone-releasing factor (GRF) regulates GH release and somatot rope proliferation via a specific G-protein-coupled receptor. Little i s known about the endocrine factors that regulate the expression of th e GRF receptor (GRF-R) in the pituitary gland. We have developed a sen sitive solution hybridization/RNAse protection assay for GRF-R mRNA in rat pituitary extracts. GRF-R transcripts were readily detectable in similar amounts in normal male and female rats, but were markedly redu ced in extracts from age-matched growth hormone (GH)-deficient dwarf ( dw) rats of either sex. The reduced GRF-R expression would appear to r eflect somatotrope hypoplasia rather than GH deficiency per se since a similar reduction in GRF-R expression was seen in a transgenic model of dominant dwarfism, whereas GRF-R expression was significantly eleva ted in rats with GH deficiency induced by hypothyroidism. We were unab le to demonstrate significant effects on GRF-R expression with infusio ns of human GH (hGH) or insulin-like growth factor 1, which stimulate growth in dw rats, but dexamethasone treatment induced a significant, time-related increase in GRF-R mRNA levels. We conclude that this assa y can usefully quantify pituitary GRF-R expression in normal rats, and its reduction in two different strains of mutant dwarf rats with soma totrope hypoplasia.