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Oxytocin neurons enable social transmission of maternal behaviour

Authors :
Rumi Ooyama
Dayu Lin
Grace H. Samadjopoulos
Annegret L. Falkner
Maria I. Alvarado Torres
Daniel Ramos
Naomi López Caraballo
Harper Lethin
Bianca J. Marlin
Takefumi Kikusui
Veronica E. Diaz
Sebastian L. Mendoza
Ioana Carcea
Regina M. Sullivan
Chloe J. Bair-Marshall
Katsuhiko Nishimori
Maya Opendak
Kazutaka Mogi
Youssef Zaim Wadghiri
Luisa Schuster
Justin S. Riceberg
Adam C. Mar
Jessica Minder
Joyce M. Mendoza Navarro
Shizu Hidema
Robert C. Froemke
Source :
Nature
Publication Year :
2021
Publisher :
Nature Publishing Group UK, 2021.

Abstract

Maternal care, including by non-biological parents, is important for offspring survival1–8. Oxytocin1,2,9–15, which is released by the hypothalamic paraventricular nucleus (PVN), is a critical maternal hormone. In mice, oxytocin enables neuroplasticity in the auditory cortex for maternal recognition of pup distress15. However, it is unclear how initial parental experience promotes hypothalamic signalling and cortical plasticity for reliable maternal care. Here we continuously monitored the behaviour of female virgin mice co-housed with an experienced mother and litter. This documentary approach was synchronized with neural recordings from the virgin PVN, including oxytocin neurons. These cells were activated as virgins were enlisted in maternal care by experienced mothers, who shepherded virgins into the nest and demonstrated pup retrieval. Virgins visually observed maternal retrieval, which activated PVN oxytocin neurons and promoted alloparenting. Thus rodents can acquire maternal behaviour by social transmission, providing a mechanism for adapting the brains of adult caregivers to infant needs via endogenous oxytocin.<br />Behavioural studies and neural recordings in mice show that virgin mice can acquire maternal behaviour through an oxytocin-dependent mechanism.

Details

Language :
English
ISSN :
14764687 and 00280836
Volume :
596
Issue :
7873
Database :
OpenAIRE
Journal :
Nature
Accession number :
edsair.doi.dedup.....4f454fb43c48bec71d1053683af13530