Title
Functional New World monkey oxytocin forms elicit an altered signaling profile and promotes parental care in rats
Date Issued
22 August 2017
Access level
open access
Resource Type
journal article
Author(s)
Parreiras-E-Silva L.T.
Vargas-Pinilla P.
Duarte D.A.
Longo D.
Finkler A.D.
Paixão-Côrtes V.R.
Paré P.
Rovaris D.L.
Oliveira E.B.
Caceres R.A.
Gonçalves G.L.
Bouvier M.
Salzano F.M.
Lucion A.B.
Costa-Neto C.M.
Bortolini M.C.
Universidade Federal do Rio Grande
Publisher(s)
National Academy of Sciences
Abstract
The neurohormone oxytocin is a key player in the modulation of reproductive and social behavioral traits, such as parental care. Recently, a correlation between different forms of oxytocin and behavioral phenotypes has been described in the New World Monkeys (NWMs). Here, we demonstrate that, compared with the Leu8OXT found in most placental mammals, the Cebidae Pro8OXT and Saguinus Val3Pro8OXT taxon-specific variants act as equi-efficacious agonists for the Gq-dependent pathway but are weaker agonists for the β-arrestin engagement and subsequent endocytosis toward the oxytocin receptor (OXTR). Upon interaction with the AVPR1a, Pro8OXT and the common Leu8OXT yielded similar signaling profiles, being equally efficacious on Gq and β-arrestin, while Val3Pro8OXT showed reduced relative efficacy toward β-arrestin. Intranasal treatment with either of the variants increased maternal behavior and also promoted unusual paternal care in rats, as measured by pup-retrieval tests. We therefore suggest that Val3Pro8OXT and Pro8OXT are functional variants, which might have been evolutionarily co-opted as an essential part of the adaptive genetic repertoire that allowed the emergence of taxon-specific complex social behaviors, such as intense parental care in the Cebidae and the genus Saguinus.
Start page
9044
End page
9049
Volume
114
Issue
34
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular Neurología clínica
Scopus EID
2-s2.0-85027892935
PubMed ID
Source
Proceedings of the National Academy of Sciences of the United States of America
ISSN of the container
00278424
Sponsor(s)
ACKNOWLEDGMENTS. This work was supported by Fundação de Pesquisa do Estado de São Paulo (FAPESP) Grant 2012/20148-0; by Canadian Institute for Health Research Grant FDN-148431; and by the Coordenação de Aperfeiçoa-mento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, and Fundação de Amparo à Pesquisa do Estado do Rio Grande do Rio Grande do Sul. M.B. holds a Canada Research Chair in in Signal Transduction and Molecular Pharmacology and is a Fellow of the Canadian Institute for Advanced Research. C.M.C.-N. and M.B. are recipients of Joint International Cooperation Grant SPRINT 2015/50086-4 funded by the FAPESP. Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/20148-0 FAPESP Coordenação de Aperfeiçoamento de Pessoal de Nível Superior CAPES Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul SPRINT 2015/50086-4 FAPERGS
Sources of information: Directorio de Producción Científica Scopus