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Author Notes:

J.K. Rilling, Department of Anthropology, Emory University, USA. Email: jrillin@emory.edu

ML and JKR conceived the study, ML collected and analyzed data and wrote the paper, AL analyzed data and wrote the paper, NL analyzed data, JKR supervised data analysis and wrote the paper.

Wenner-Gren Dissertation Fieldwork Grant (USA)- Grant number: Gr. (9827). Silvio O Conte Center for Oxytocin and Social Cognition Pilot Research Grant (USA) - Grant number: (P50MH100023). Emory Facility for Education and Research in Neuroscience Educational Grant (USA). We thank Drs. Larry Young, Melvin Konner, and Gregory Berns for their helpful feedback. We also thank Lynnet Richey, Amber Gonzalez, and Jenna Shin for their help with various aspects of the study.

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Subjects:

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Endocrinology & Metabolism
  • Neurosciences
  • Psychiatry
  • Neurosciences & Neurology
  • OXTR
  • Multi -locus genetic profile score
  • Social conformity
  • Moral values
  • pMFC
  • Internal conflict
  • PREDICTS
  • INFORMATION
  • COOPERATION
  • EXPRESSION
  • SALIENCE
  • ACCURATE
  • CORTEX
  • ROBUST

Enhanced endogenous oxytocin signaling in the brain modulates neural responses to social misalignment and promotes conformity in humans: A multi-locus genetic profile approach

Tools:

Journal Title:

PSYCHONEUROENDOCRINOLOGY

Volume:

Volume 144

Publisher:

, Pages 105869-105869

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The neuropeptide oxytocin (OT) is known to promote social conformity. However, the specific neurocognitive mechanisms underlying OT-induced conformity remain unclear. We aimed to address this gap by examining how genetic variation in the oxytocin receptor gene (OXTR) is linked with behavioral conformity and its underlying neural systems. Specifically, we utilized the genotype-tissue expression database (GTEx) to create a novel multi-locus genetic profile score (MPS) that reflects the level of OXTR expression in the human brain. A total of 194 participants (Neuroimaging N = 50, Behavioral N = 144) performed a novel conformity task in which they viewed a series of word pairs depicting various moral values and virtues widely recognized in the United States. In each trial, participants indicated the relative importance of these words and subsequently learned about the majority opinion. Participants later rated the same word pairs a second time. Changes in participants’ ratings between the first and second sessions were measured and analyzed with respect to social feedback, blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) signals, and OXTR MPS. We found that participants adjusted their ratings in accordance with the majority opinions. Social misalignment between self and others activated brain areas such as the striatum and the posterior medial frontal cortex (pMFC). However, unlike most findings from previous studies, activation in the pMFC during the inconsistent social feedback negatively, rather than positively, predicted behavioral conformity. Notably, those with higher OXTR MPS had reduced pMFC activation in the face of social misalignment, which led to greater conformity. Our findings suggest that OT may promote conformity by dampening the conflict-related signals in the pMFC. They also show that OXTR MPS may be useful for studying the effect of genes on highly complex human social traits, such as conformity.

Copyright information:

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License (https://creativecommons.org/licenses/by-nc-sa/4.0/).
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