Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Mar 5:4:20.
doi: 10.3389/fendo.2013.00020. eCollection 2013.

Physiological Roles of GPR10 and PrRP Signaling

Affiliations

Physiological Roles of GPR10 and PrRP Signaling

Garron T Dodd et al. Front Endocrinol (Lausanne). .

Abstract

Prolactin-releasing peptide (PrRP) was first isolated from bovine hypothalamus, and was found to act as an endogenous ligand at the G-protein-coupled receptor 10 (GPR10 or hGR3). Although originally named as it can affect the secretion of prolactin from anterior pituitary cells, the potential functions for this peptide have been greatly expanded over the past decade. Anatomical, pharmacological, and physiological studies indicate that PrRP, signaling via the GPR10 receptor, may have a wide range of roles in neuroendocrinology; such as in energy homeostasis, stress responses, cardiovascular regulation, and circadian function. This review will provide the current knowledge of the PrRP and GPR10 signaling system, its putative functions, implications for therapy, and future perspectives.

Keywords: GPR10; PrRP; dorsomedial hypothalamic nucleus; energy intake; energy metabolism; nucleus tractus solitarius; stress.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Schematic drawings showing the neuronal distribution of PrRP and GPR10 receptor in the Paxions and Watson rat brain atlas (Paxinos and Watson, ; Sun et al., 2005). Blue areas represent PrRP-immunopositive nerve fibers; black checkers represent PrRP cells bodies; green areas represent GPR10 expression; and red areas represent overlap of PrRP and GPR10 expression. AP, area postrema; BL, basolateral amygdaloid nucleus; BNST, bed nucleus of the stria terminalis; Ce, central amygdaloid nucleus; DMN, dorsomedial hypothalamic nucleus; LH, lateral hypothalamic area; MCPO, magnocellular preoptic nucleus; MD, mediodorsal thalamic nucleus; MPO, medial preoptic nucleus; ox, optic chiasm; PVN, paraventricular hypothalamic nucleus; Pe, periventricular hypothalamic nucleus; PT, paratenial thalamic nucleus; Rt, reticular thalamic nucleus; SM, nucleus of the stria medullaris; SO, supraoptic hypothalamic nucleus; NTS, nucleus of the tractus solitarius; SpVe, spinal vestibular nucleus; VLH, ventrolateral hypothalamic nucleus.

References

    1. Aicher S. A., Kurucz O. S., Reis D. J., Milner T. A. (1995). Nucleus tractus solitarius efferent terminals synapse on neurons in the caudal ventrolateral medulla that project to the rostral ventrolateral medulla. Brain Res. 693, 51–6310.1016/0006-8993(95)00660-I - DOI - PubMed
    1. Bechtold D. A., Luckman S. M. (2006). Prolactin-releasing peptide mediates cholecystokinin-induced satiety in mice. Endocrinology 147, 4723–472910.1210/en.2006-0753 - DOI - PubMed
    1. Bechtold D. A., Luckman S. M. (2007). The role of RFamide peptides in feeding. J. Endocrinol. 192, 3–1510.1677/JOE-06-0069 - DOI - PubMed
    1. Bechtold D. A., Sidibe A., Saer B. R., Li J., Hand L. E., Ivanova E. A., et al. (2012). A role for the melatonin-related receptor GPR50 in leptin signaling, adaptive thermogenesis, and torpor. Curr. Biol. 22, 70–7710.1016/j.cub.2011.11.043 - DOI - PubMed
    1. Bhattacharyya S., Luan J., Challis B., Schmitz C., Clarkson P., Franks P. W., et al. (2003). Association of polymorphisms in GPR10, the gene encoding the prolactin-releasing peptide receptor with blood pressure, but not obesity, in a U.K. Caucasian population. Diabetes 52, 1296–129910.2337/diabetes.52.5.1296 - DOI - PubMed

LinkOut - more resources