Regulation of Gpr173 expression, a putative phoenixin receptor, by saturated fatty acid palmitate and endocrine-disrupting chemical bisphenol A through a p38-mediated mechanism in immortalized hypothalamic neurons.
Animals
Benzhydryl Compounds
/ adverse effects
Cells, Cultured
Down-Regulation
Female
Gene Expression Regulation
/ drug effects
Hypothalamic Hormones
/ pharmacology
Hypothalamus
/ cytology
MAP Kinase Signaling System
/ drug effects
Male
Mice
Neurons
/ cytology
Palmitates
/ adverse effects
Phenols
/ adverse effects
Phosphorylation
/ drug effects
Receptors, G-Protein-Coupled
/ genetics
Cell biology
Endocrine-disrupting
Gene expression
Hypothalamus
Phoenixin receptor
Journal
Molecular and cellular endocrinology
ISSN: 1872-8057
Titre abrégé: Mol Cell Endocrinol
Pays: Ireland
ID NLM: 7500844
Informations de publication
Date de publication:
05 04 2019
05 04 2019
Historique:
received:
11
10
2018
revised:
31
01
2019
accepted:
31
01
2019
pubmed:
5
2
2019
medline:
18
12
2019
entrez:
5
2
2019
Statut:
ppublish
Résumé
GPR173 is a highly conserved G protein coupled receptor associated with the hypothalamic-pituitary-gonadal reproductive axis. It is expressed in the brain and ovaries, however considerable knowledge about its function remains unknown. One putative ligand for this receptor is phoenixin (PNX), a newly identified reproductive peptide involved in hypothalamic coordination of the estrous cycle. In order to characterize GPR173, it is vital to determine how Gpr173 is regulated in the hypothalamus. Since the hypothalamus senses compounds from the blood, such as nutrients and chemicals, we examined the effect of palmitate, a saturated fatty acid, and bisphenol A (BPA), an endocrine disrupting chemical, on Gpr173 gene expression. Immortalized hypothalamic neurons were treated with palmitate or BPA for 2-24 h and Gpr173 mRNA levels were assessed with RT-qPCR. Palmitate and BPA both reduced Gpr173 mRNA levels, in part through the mitogen-activated protein kinase (MAPK), p38. Pre-treatment with palmitate for 24 h blocked the PNX-induction of phosphorylated cAMP response element-binding protein (CREB) levels. In conclusion, nutrition levels and environmental chemicals may influence reproductive function through modulation of Gpr173 expression, which may prove to be a future therapeutic target in reproductive health.
Identifiants
pubmed: 30716364
pii: S0303-7207(19)30038-3
doi: 10.1016/j.mce.2019.01.026
pii:
doi:
Substances chimiques
Benzhydryl Compounds
0
GPR173 protein, mouse
0
Hypothalamic Hormones
0
Palmitates
0
Phenols
0
Receptors, G-Protein-Coupled
0
bisphenol A
MLT3645I99
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
54-60Subventions
Organisme : CIHR
Pays : Canada
Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.