Cited by 89Pain Mechanisms and TreatmentsNeural and Behavioral Psychology StudiesPsychosomatic Disorders and Their Treatments

Pain-related effects of trait anger expression: Neural substrates and the role of endogenous opioid mechanisms

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Bruehl, Stephen, Burns, John W., Chung, Ok Y., Chont, Melissa·2009·Neuroscience & Biobehavioral Reviews

Abstract

Literature is reviewed indicating that greater tendency to manage anger via direct verbal or physical expression (trait anger-out) is associated with increased acute and chronic pain responsiveness. Neuroimaging data are overviewed supporting overlapping neural circuits underlying regulation of both pain and anger, consisting of brain regions including the rostral anterior cingulate cortex, orbitofrontal cortex, anterior insula, amygdala, and periaqueductal gray. These circuits provide a potential neural basis for observed positive associations between anger-out and pain responsiveness. The role of endogenous opioids in modulating activity in these interlinked brain regions is explored, and implications for understanding pain-related effects of anger-out are described. An opioid dysfunction hypothesis is presented in which inadequate endogenous opioid inhibitory activity in these brain regions contributes to links between trait anger-out and pain. A series of studies is presented that supports the opioid dysfunction hypothesis, further suggesting that gender and genetic factors may moderate these effects. Finally, possible implications of interactions between trait anger-out and state behavioral anger expression on endogenous opioid analgesic activity are described.

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Crossref · 10.1016/j.neubiorev.2008.12.003

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  • More than 80% of published studies indicate that elevated trait anger-out is associated with greater chronic pain intensity and greater chronic pain-related dysfunction.

    “Although some null findings have been reported, more than 80% of published studies indicate that elevated trait anger-out is associated with greater CP intensity and greater CP-related dysfunction.61”

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  1. Adler LJ Gyulai FE Diehl DJ Mintun MA Winter PM Firestone LL Regional brain activity changes associated with fentanyl analgesia elucidated by positron emission tomography. Anesth. Analg 1997 84 120 126 8989012

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Authors
Bruehl, S., Burns, J. W., Chung, O. Y., & Chont, M.
Affiliations
  • Vanderbilt University (US)
  • Rosalind Franklin University of Medicine and Science (US)
Corresponding author
Bruehl, Stephen
Venue
Neuroscience & Biobehavioral Reviews
Publisher
Elsevier BV
Published
2009-03
Volume
33
Issue
3
Pages
475-491
ISSN
0149-7634 (ISSN-L)
OpenAlex
W2010965582
Cited by
88
References
154
Citations by year
2026: 1 · 2025: 4 · 2024: 3 · 2023: 2 · 2022: 4 · 2021: 5 · 2020: 2 · 2019: 2 · 2018: 4 · 2017: 8 · 2016: 4 · 2015: 6 · 2014: 6 · 2013: 13 · 2012: 8
FWCI
3.61
Type
journal article
Language
en
Open access
Locations
  • Neuroscience & Biobehavioral Reviews (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute of Mental Health (R01MH071260)
  • National Institute of Neurological Disorders and Stroke (R01NS038145, R01NS046694, R01NS050578)
  • National Center for Research Resources (M01RR000095, RR00095)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (P30HD015052, P30 HD-15052)
Topics
  • Health Sciences › Medicine › Physiology › Pain Mechanisms and Treatments
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
Keywords
anger-out, endogenous opioids, pain modulation, neural circuits, rostral anterior cingulate cortex, orbitofrontal cortex, anterior insula, amygdala, periaqueductal gray, gender differences, genetic factors, analgesia
MeSH terms
Analgesics, Opioid, Anger, Brain, Brain Mapping, Humans, Magnetic Resonance Imaging, Neural Pathways, Pain, Sex Characteristics, Pain Threshold, Opioid Peptides, Expressed Emotion, Positron-Emission Tomography

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