Estrous Cycle Modulation of Feeding and Relaxin-3/Rxfp3 mRNA Expression: Implications for Estradiol Action.


Journal

Neuroendocrinology
ISSN: 1423-0194
Titre abrégé: Neuroendocrinology
Pays: Switzerland
ID NLM: 0035665

Informations de publication

Date de publication:
2021
Historique:
received: 29 09 2020
accepted: 14 12 2020
pubmed: 18 12 2020
medline: 1 2 2022
entrez: 17 12 2020
Statut: ppublish

Résumé

Food intake varies during the ovarian hormone/estrous cycle in humans and rodents, an effect mediated mainly by estradiol. A potential mediator of the central anorectic effects of estradiol is the neuropeptide relaxin-3 (RLN3) synthetized in the nucleus incertus (NI) and acting via the relaxin family peptide-3 receptor (RXFP3). We investigated the relationship between RLN3/RXFP3 signaling and feeding behavior across the female rat estrous cycle. We used in situ hybridization to investigate expression patterns of Rln3 mRNA in NI and Rxfp3 mRNA in the hypothalamic paraventricular nucleus (PVN), lateral hypothalamic area (LHA), medial preoptic area (MPA), and bed nucleus of the stria terminalis (BNST), across the estrous cycle. We identified expression of estrogen receptors (ERs) in the NI using droplet digital PCR and assessed the electrophysiological responsiveness of NI neurons to estradiol in brain slices. Rln3 mRNA reached the lowest levels in the NI pars compacta during proestrus. Rxfp3 mRNA levels varied across the estrous cycle in a region-specific manner, with changes observed in the perifornical LHA, magnocellular PVN, dorsal BNST, and MPA, but not in the parvocellular PVN or lateral LHA. G protein-coupled estrogen receptor 1 (Gper1) mRNA was the most abundant ER transcript in the NI. Estradiol inhibited 33% of type 1 NI neurons, including RLN3-positive cells. These findings demonstrate that the RLN3/RXFP3 system is modulated by the estrous cycle, and although further studies are required to better elucidate the cellular and molecular mechanisms of estradiol signaling, current results implicate the involvement of the RLN3/RXFP3 system in food intake fluctuations observed across the estrous cycle in female rats.

Identifiants

pubmed: 33333517
pii: 000513830
doi: 10.1159/000513830
doi:

Substances chimiques

Nerve Tissue Proteins 0
RLN3 protein, rat 0
RNA, Messenger 0
RXFP3 protein, rat 0
Receptors, G-Protein-Coupled 0
Receptors, Peptide 0
Estradiol 4TI98Z838E
Relaxin 9002-69-1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1201-1218

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Camila de Ávila (C)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada, Avila.Camila@mayo.edu.
Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark, Avila.Camila@mayo.edu.
Department of Neuroscience, Mayo Clinic, Scottsdale, Arizona, USA, Avila.Camila@mayo.edu.
Department of Psychology, Arizona State University, Tempe, Arizona, USA, Avila.Camila@mayo.edu.

Sandrine Chometton (S)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada.

Juliane Calvez (J)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada.

Geneviève Guèvremont (G)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada.

Alan Kania (A)

Department of Neurophysiology and Chronobiology, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.

Lola Torz (L)

Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
NNF CBMR, Nutrient and Metabolite Sensing, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark.

Christophe Lenglos (C)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada.

Anna Blasiak (A)

Department of Neurophysiology and Chronobiology, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.

Mette M Rosenkilde (MM)

Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Birgitte Holst (B)

Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
NNF CBMR, Nutrient and Metabolite Sensing, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark.

Cheryl D Conrad (CD)

Department of Psychology, Arizona State University, Tempe, Arizona, USA.

John D Fryer (JD)

Department of Neuroscience, Mayo Clinic, Scottsdale, Arizona, USA.

Elena Timofeeva (E)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada.

Andrew L Gundlach (AL)

The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.

Carlo Cifani (C)

Department of Psychiatry and Neuroscience, Faculty of Medicine, CRIUCPQ, Université Laval, Québec, Québec, Canada.
School of Pharmacy, Pharmacology Unit, University of Camerino, Camerino, Italy.

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Classifications MeSH