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The effect of intranasal oxytocin on social reward processing in humans: a systematic review

Journal

FRONTIERS IN PSYCHIATRY
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2023.1244027

Keywords

oxytocin; social reward; anticipation; consumption; social motivation; wanting; liking; fMRI

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Understanding the neurobiology of social reward processing is crucial for reducing maladaptive social behaviors and enhancing healthy social life. Current research suggests that oxytocin plays a role in the processing of social rewards. However, studies in humans have shown mixed results. This review summarizes 19 studies that investigated the effects of intranasal oxytocin administration on social reward processing. The findings indicate that oxytocin is most effective during the consumption phase of social rewards and may modulate the activity of several brain regions.
Understanding the neurobiology of social reward processing is fundamental, holding promises for reducing maladaptive/dysfunctional social behaviors and boosting the benefits associated with a healthy social life. Current research shows that processing of social (vs. non-social) rewards may be driven by oxytocinergic signaling. However, studies in humans often led to mixed results. This review aimed to systematically summarize available experimental results that assessed the modulation of social reward processing by intranasal oxytocin (IN-OXY) administration in humans. The literature search yielded 385 results, of which 19 studies were included in the qualitative synthesis. The effects of IN-OXY on subjective, behavioral, and (neuro)physiological output variables are discussed in relation to moderating variables-reward phase, reward type, onset and dosage, participants' sex/gender, and clinical condition. Results indicate that IN-OXY is mostly effective during the consumption (liking) of social rewards. These effects are likely exerted by modulating the activity of the prefrontal cortex, insula, precuneus, anterior cingulate cortex, amygdala, and striatum. Finally, we provide suggestions for designing future oxytocin studies.

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