Adolescents growing up amidst intractable conflict attenuate brain response to pain of outgroup

Proc Natl Acad Sci U S A. 2016 Nov 29;113(48):13696-13701. doi: 10.1073/pnas.1612903113. Epub 2016 Nov 14.

Abstract

Adolescents' participation in intergroup conflicts comprises an imminent global risk, and understanding its neural underpinnings may open new perspectives. We assessed Jewish-Israeli and Arab-Palestinian adolescents for brain response to the pain of ingroup/outgroup protagonists using magnetoencephalography (MEG), one-on-one positive and conflictual interactions with an outgroup member, attitudes toward the regional conflict, and oxytocin levels. A neural marker of ingroup bias emerged, expressed via alpha modulations in the somatosensory cortex (S1) that characterized an automatic response to the pain of all protagonists followed by rebound/enhancement to ingroup pain only. Adolescents' hostile social interactions with outgroup members and uncompromising attitudes toward the conflict influenced this neural marker. Furthermore, higher oxytocin levels in the Jewish-Israeli majority and tighter brain-to-brain synchrony among group members in the Arab-Palestinian minority enhanced the neural ingroup bias. Findings suggest that in cases of intractable intergroup conflict, top-down control mechanisms may block the brain's evolutionary-ancient resonance to outgroup pain, pinpointing adolescents' interpersonal and sociocognitive processes as potential targets for intervention.

Keywords: alpha oscillations; brain-to-brain synchrony; empathy; intergroup conflict; oxytocin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Arabs / psychology
  • Attitude
  • Brain / metabolism
  • Brain / physiology*
  • Brain Mapping
  • Empathy / physiology
  • Female
  • Humans
  • Interpersonal Relations*
  • Israel
  • Jews / psychology
  • Magnetoencephalography
  • Male
  • Middle East
  • Minority Groups / psychology
  • Oxytocin / metabolism
  • Politics*
  • Somatosensory Cortex / physiology*

Substances

  • Oxytocin