Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery

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...

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Veröffentlicht in:Endocrinology (Philadelphia) 1999-12, Vol.140 (12), p.5736-5745
Hauptverfasser: Roland, Barbara L, Sutton, Steven W, Wilson, Sandy J, Luo, Lin, Pyati, Jayashree, Huvar, Rene, Erlander, Mark G, Lovenberg, Timothy W
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container_end_page 5745
container_issue 12
container_start_page 5736
container_title Endocrinology (Philadelphia)
container_volume 140
creator Roland, Barbara L
Sutton, Steven W
Wilson, Sandy J
Luo, Lin
Pyati, Jayashree
Huvar, Rene
Erlander, Mark G
Lovenberg, Timothy W
description 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.
doi_str_mv 10.1210/endo.140.12.7211
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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. 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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. 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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.</abstract><cop>Washington</cop><pub>Endocrine Society</pub><doi>10.1210/endo.140.12.7211</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Adrenal medulla
Affinity
Agonists
Amino acid substitution
Amino acids
Antagonists
Area postrema
Autonomic nervous system
Binding
Calcium mobilization
Central nervous system
Citrulline
Feedback control
Homeostasis
Hybridization
Hypothalamus
Hypothalamus (anterior)
Hypothalamus (dorsomedial)
Intestine
Lysine
mRNA
Nervous system
Neuropeptides
Nuclei (cytology)
Peptides
Pharmacology
Pituitary (anterior)
Prolactin
Prolactin-releasing peptide
Receptors
Releasing
Solitary tract nucleus
Thalamic reticular nucleus
Thalamus
title Anatomical Distribution of Prolactin-Releasing Peptide and Its Receptor Suggests Additional Functions in the Central Nervous System and Periphery
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