BIOSOCIOCOG

Oxytocin and Dopamine Interplay in Humans – on the Biology of Social Cognition

 Coordinatore INSTITUTO DE MEDICINA MOLECULAR 

 Organization address address: AVENIDA PROF EGAS MONIZ
city: LISBOA
postcode: 1649 028

contact info
Titolo: Dr.
Nome: Joana
Cognome: Costa
Email: send email
Telefono: +351 217999565
Fax: +351 217999412

 Nazionalità Coordinatore Portugal [PT]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2015
 Periodo (anno-mese-giorno) 2015-01-01   -   2018-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUTO DE MEDICINA MOLECULAR

 Organization address address: AVENIDA PROF EGAS MONIZ
city: LISBOA
postcode: 1649 028

contact info
Titolo: Dr.
Nome: Joana
Cognome: Costa
Email: send email
Telefono: +351 217999565
Fax: +351 217999412

PT (LISBOA) coordinator 100˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

acute    social    human    dopamine    trust    dopaminergic    reward    oxytocin    striatal    oxytocinergic    cognition    chronic    predispositions   

 Obiettivo del progetto (Objective)

'This project asks ‘Do oxytocin and dopamine systems interact in the human brain?’. It will encompass an innovative, inter- disciplinary method combining established techniques in neuropharmacology, neuroimaging and genetics. It will use a mentalizing (social dilemma) task where it is hypothesized that the trust-eliciting reward value of mutual cooperation is coded by both dopaminergic and oxytocinergic actions in the striatum. Support for this comes from dopamine´s well-characterized role in reward learning and oxytocin’s recently found impact on affiliate and cooperative behavior and its neurocorrelates. As a way of assessing these systems, I will combine, for the first time, oxytocin and dopamine manipulations; as well as integrate information from natural genetic variability to further support my predictions. The underlying assumption is that acute changes in their striatal levels as well as chronic predispositions affecting their systems can influence striatal activation during social reward processing. (Chronic predispositions arising from environmental historical events and personality will also be taken into account.)

There is robust evidence that interplay between the dopamine and the oxytocine systems is crucial for social cognition from animal studies, however this has not yet been investigated in humans. The question is paramount and timely as mental illness enigmas involving trust/paranoia, social avolition and anxiety or drug addiction are still unresolved and new oxytocinergic therapies are now being clinically trialed for autism and schizophrenia (and partially to complement dopaminergic ones, as in the case of the latter). The ultimate goal herein is to inform the rational design of treatments for these conditions by better understanding the biological underpinnings of human social cognition, in respect to trust and social behaviour.'

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