Anatomical distribution of prolactin-releasing peptide and its receptor suggests additional functions in the central nervous system and periphery

被引:167
作者
Roland, BL [1 ]
Sutton, SW [1 ]
Wilson, AJ [1 ]
Luo, L [1 ]
Pyati, J [1 ]
Huvar, R [1 ]
Erlander, MG [1 ]
Lovenberg, TW [1 ]
机构
[1] RW Johnson Pharmaceut Res Inst, San Diego, CA 92121 USA
关键词
D O I
10.1210/en.140.12.5736
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页码:5736 / 5745
页数:10
相关论文
共 22 条
[1]   NEUROENDOCRINE REGULATION OF PROLACTIN-RELEASE [J].
BENJONATHAN, N ;
ARBOGAST, LA ;
HYDE, JF .
PROGRESS IN NEUROBIOLOGY, 1989, 33 (5-6) :399-447
[2]  
Bernardis LL, 1998, P SOC EXP BIOL MED, V218, P284
[3]   ACTIONS OF BOMBESIN, THYROTROPIN RELEASING FACTOR, PROSTAGLANDIN-E2 AND NALOXONE ON THERMOREGULATION IN RAT [J].
BROWN, M ;
RIVIER, J ;
VALE, W .
LIFE SCIENCES, 1977, 20 (10) :1681-1687
[4]   THYROTROPIN RELEASING-FACTOR - A PUTATIVE CNS REGULATOR OF THE AUTONOMIC NERVOUS-SYSTEM [J].
BROWN, MR .
LIFE SCIENCES, 1981, 28 (15-1) :1789-1795
[5]   SPATIALLY AND TEMPORALLY DIFFERENTIATED PATTERNS OF C-FOS EXPRESSION IN BRAIN-STEM CATECHOLAMINERGIC CELL GROUPS INDUCED BY CARDIOVASCULAR CHALLENGES IN THE RAT [J].
CHAN, RKW ;
SAWCHENKO, PE .
JOURNAL OF COMPARATIVE NEUROLOGY, 1994, 348 (03) :433-460
[6]   Prolactin-releasing peptide-immunoreactivity in A1 and A2 noradrenergic neurons of the rat medulla [J].
Chen, CT ;
Dun, SL ;
Dun, NJ ;
Chang, JK .
BRAIN RESEARCH, 1999, 822 (1-2) :276-279
[7]  
DELAESCALERA GM, 1988, NEUROENDOCRINOLOGY, V47, P576
[8]   Isolation and characterization of a novel bioactive peptide, Carassius RFamide (C-RFa), from the brain of the Japanese crucian carp [J].
Fujimoto, M ;
Takeshita, K ;
Wang, XY ;
Takabatake, I ;
Fujisawa, Y ;
Teranishi, H ;
Ohtani, M ;
Muneoka, Y ;
Ohta, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 242 (02) :436-440
[9]   A prolactin-releasing peptide in the brain [J].
Hinuma, S ;
Habata, Y ;
Fujii, R ;
Kawamata, Y ;
Hosoya, N ;
Fukusumi, S ;
Kitada, C ;
Masuo, Y ;
Asano, T ;
Matsumoto, H ;
Sekiguchi, M ;
Kurokawa, T ;
Nishimura, O ;
Onda, H ;
Fujino, M .
NATURE, 1998, 393 (6682) :272-276
[10]   MEDULLARY THYROTROPIN-RELEASING-HORMONE MEDIATES VAGAL-DEPENDENT ADAPTIVE GASTRIC PROTECTION INDUCED BY MILD ACID IN RATS [J].
KANEKO, H ;
KATO, K ;
OHNING, G ;
TACHE, Y .
GASTROENTEROLOGY, 1995, 109 (03) :861-865