Literature DB >> 31178317

Oxytocin Signaling in the Central Amygdala Modulates Emotion Discrimination in Mice.

Valentina Ferretti1, Federica Maltese1, Gabriella Contarini1, Marco Nigro1, Alessandra Bonavia1, Huiping Huang1, Valentina Gigliucci2, Giovanni Morelli3, Diego Scheggia1, Francesca Managò1, Giulia Castellani1, Arthur Lefevre4, Laura Cancedda3, Bice Chini2, Valery Grinevich4, Francesco Papaleo5.   

Abstract

Recognition of other's emotions influences the way social animals interact and adapt to the environment. The neuropeptide oxytocin (OXT) has been implicated in different aspects of emotion processing. However, the role of endogenous OXT brain pathways in the social response to different emotional states in conspecifics remains elusive. Here, using a combination of anatomical, genetic, and chemogenetic approaches, we investigated the contribution of endogenous OXT signaling in the ability of mice to discriminate unfamiliar conspecifics based on their emotional states. We found that OXTergic projections from the paraventricular nucleus of the hypothalamus (PVN) to the central amygdala (CeA) are crucial for the discrimination of both positively and negatively valenced emotional states. In contrast, blocking PVN OXT release into the nucleus accumbens, prefrontal cortex, and hippocampal CA2 did not alter this emotion discrimination. Furthermore, silencing each of these PVN OXT pathways did not influence basic social interaction. These findings were further supported by the demonstration that virally mediated enhancement of OXT signaling within the CeA was sufficient to rescue emotion discrimination deficits in a genetic mouse model of cognitive liability. Our results indicate that CeA OXT signaling plays a key role in emotion discrimination both in physiological and pathological conditions.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  DREADDs; amygdala; brain circuits; dysbindin-1; fear; relief; social cognition

Mesh:

Substances:

Year:  2019        PMID: 31178317     DOI: 10.1016/j.cub.2019.04.070

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  42 in total

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