scholarly journals Social Exclusion Modulates Neural Dynamics of Monetary and Social Reward Processing

2021 ◽  
Vol 168 ◽  
pp. S175
Author(s):  
Mengsi Xu ◽  
Zhenhong Wang
2020 ◽  
Vol 226 ◽  
pp. 129-137 ◽  
Author(s):  
Andrea Pelletier-Baldelli ◽  
Joseph M. Orr ◽  
Jessica A. Bernard ◽  
Vijay A. Mittal

2020 ◽  
Author(s):  
Daniel Sazhin ◽  
Angelique Frazier ◽  
Caleb River Haynes ◽  
Camille Johnston ◽  
Iris Ka-Yi Chat ◽  
...  

This report describes an ongoing R03 grant that explores the links between trait reward sensitivity, substance use, and neural responses to social and nonsocial reward. Although previous research has shown that trait reward sensitivity and neural responses to reward are linked to substance use, whether this relationship is impacted by how people process social stimuli remains unclear. We are investigating these questions via a neuroimaging study with college-aged participants, using individual difference measures that examine the relation between substance use, social context, and trait reward sensitivity with tasks that measure reward anticipation, strategic behavior, social reward consumption, and the influence of social context on reward processing. We predict that substance use will be tied to distinct patterns of striatal dysfunction. Specifically, reward hyposensitive individuals will exhibit blunted striatal responses to social and non-social reward and enhanced connectivity with the orbitofrontal cortex; in contrast, reward hypersensitive individuals will exhibit enhanced striatal responses to social and non-social reward and blunted connectivity with the orbitofrontal cortex. We also will examine the relation between self-reported reward sensitivity, substance use, and striatal responses to social reward and social context. We predict that individuals reporting the highest levels of substance use will show exaggerated striatal responses to social reward and social context, independent of self-reported reward sensitivity. Examining corticostriatal responses to reward processing will help characterize the relation between reward sensitivity, social context and substance use while providing a foundation for understanding risk factors and isolating neurocognitive mechanisms that may be targeted to increase the efficacy of interventions.


2019 ◽  
Vol 15 (1) ◽  
pp. 83-97 ◽  
Author(s):  
Youngbin Kwak ◽  
Xing-Jie Chen ◽  
Kelsey McDonald ◽  
Brynn Boutin

2018 ◽  
Author(s):  
Xiaole Ma ◽  
Weihua Zhao ◽  
Ruixue Luo ◽  
Feng Zhou ◽  
Yayuan Geng ◽  
...  

AbstractWe interact socially and form bonds with others because such experiences are rewarding. However, an insecure attachment style or social anxiety can reduce these rewarding effects. The neuropeptide oxytocin (OXT) may facilitate social interactions either by increasing their rewarding experience or by attenuating anxiety, although effects can be sex- and attachment-style dependent. In this study, 64 pairs of same-sex friends completed a social sharing paradigm in a double-blind, placebo-controlled, between-subject design with one friend inside an MRI scanner and the other in a remote behavioral testing room. In this way we could examine whether intranasal-OXT differentially modulated the emotional impact of social sharing and associated neural processing. Additionally, we investigated if OXT effects were modulated by sex and attachment style. Results showed that in women, but not men, OXT increased ratings for sharing stimuli with their friend but not with a stranger, particularly in the friend in the scanner. Corresponding neuroimaging results showed that OXT decreased both amygdala and insula activity as well as their functional connectivity in women when they shared with friends but had the opposite effect in men. On the other hand, OXT did not enhance responses in brain reward circuitry. In the PLC treated group amygdala responses in women when they shared pictures with their friend were positively associated with attachment anxiety and OXT uncoupled this. Our findings demonstrate that OXT facilitates the impact of sharing positive experiences with others in women, but not men, and that this is associated with differential effects on the amygdala and insula and their functional connections. Furthermore, OXT particularly reduced increased amygdala responses during sharing in individuals with higher attachment anxiety. Thus, OXT effects in this context may be due more to reduced anxiety when sharing with a friend than to enhanced social reward.


Author(s):  
Leigh Sepeta ◽  
Naotsugu Tsuchiya ◽  
Mari S Davies ◽  
Marian Sigman ◽  
Susan Y Bookheimer ◽  
...  

2012 ◽  
Vol 9 (3) ◽  
pp. 367-377 ◽  
Author(s):  
John A. Richey ◽  
Alison Rittenberg ◽  
Lauren Hughes ◽  
Cara R. Damiano ◽  
Antoinette Sabatino ◽  
...  

2021 ◽  
Vol 31 (3) ◽  
pp. 703-716 ◽  
Author(s):  
Emily A. Hutchinson ◽  
Stefanie L. Sequeira ◽  
Jennifer S. Silk ◽  
Neil P. Jones ◽  
Caroline Oppenheimer ◽  
...  

Autism ◽  
2019 ◽  
Vol 24 (1) ◽  
pp. 233-245
Author(s):  
Catarina Silva ◽  
Chloé Jover ◽  
David Da Fonseca ◽  
Francisco Esteves ◽  
Christine Deruelle

Humans are commonly motivated towards cooperation and prosociality. In this study, we examined this motivational predisposition in autistic individuals. Using an adaptation of the Cyberball paradigm, we investigated subsequent pro-social behaviour after witnessing social exclusion. Participants witnessed and played a series of Cyberball games, rated their affective state and valued emotional faces with respect to their approachability. Results showed that participants from both groups were aware of the social exclusion. However, while neurotypically developing participants engaged in pro-social behaviour in reaction to the exclusion, autistic participants showed less alterations, in terms of either behaviour or affective state. The current findings suggest a distinct motivational drive and processing of social reward stimuli in autism, which may result in behavioural responses divergent from typical development when engaging in the social world.


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