Back to Search
Start Over
Anatomical distribution of prolactin-releasing peptide and its receptor suggests additional functions in the central nervous system and periphery.
- Source :
-
Endocrinology [Endocrinology] 1999 Dec; Vol. 140 (12), pp. 5736-45. - Publication Year :
- 1999
-
Abstract
- A recently identified neuropeptide with PRL-releasing capabilities binds to and activates a previously known orphan G protein-coupled receptor, GPR10. We initiated a study to define the pharmacology of the peptide/receptor interaction and to identify the distribution of the peptide and its receptor in the central nervous system to elucidate sites of action of the peptide. The PRL-releasing peptide (PrRP) is a C-terminally amidated, 31-amino acid peptide derived from a 98-amino acid precursor. Radioiodinated PrRP-(1-31) binds to its receptor with high affinity (1 nM) and stimulates calcium mobilization in CHOK1 cells stably transfected with the receptor. A series of N-terminal deletions reveals that the PrRP-(12-31) amino acid is equipotent to PrRP-(1-31). Further N-terminal deletions reduce the affinity of the ligand considerably, although PrRP-(25-31) is still able to compete for binding and behaves as an agonist. The arginine residues at position 26 and 30 are critical for binding, as substitution with either lysine or citrulline reduces the affinity substantially. In situ hybridization reveals a distinct tissue distribution for both the peptide and receptor messenger RNAs. The receptor is expressed abundantly in the reticular thalamic nucleus, periventricular hypothalamus, dorsomedial hypothalamus, nucleus of the solitary tract, area postrema, anterior pituitary, and adrenal medulla. The peptide messenger RNA is expressed in the dorsomedial hypothalamus, nucleus of the solitary tract, ventrolateral reticular nucleus, and intestine. This tissue distribution suggests an alternative function of PrRP than its purported hypophysiotropic function, such as a potential role for PrRP in the central feedback control of neuroendocrine and autonomic homeostasis. Further work using selective agonists and antagonists should help define additional physiological roles of this novel mammalian neuropeptide.
- Subjects :
- Animals
Brain metabolism
Brain Chemistry
CHO Cells
Cricetinae
Gene Expression
Hypothalamic Hormones genetics
Hypothalamic Hormones metabolism
In Situ Hybridization
Iodine Radioisotopes
Male
Neuropeptides genetics
Neuropeptides metabolism
Prolactin-Releasing Hormone
RNA, Messenger analysis
Rats
Rats, Sprague-Dawley
Receptors, Neuropeptide genetics
Receptors, Neuropeptide metabolism
Thalamic Nuclei chemistry
Thyrotropin-Releasing Hormone genetics
Tissue Distribution
Transfection
Tyrosine 3-Monooxygenase analysis
Central Nervous System chemistry
Hypothalamic Hormones analysis
Neuropeptides analysis
Receptors, Neuropeptide analysis
Subjects
Details
- Language :
- English
- ISSN :
- 0013-7227
- Volume :
- 140
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 10579339
- Full Text :
- https://doi.org/10.1210/endo.140.12.7211