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

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NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
卷 33, 期 3, 页码 475-491

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neubiorev.2008.12.003

关键词

Anger expression; Anger-out; Chronic pain; Acute pain; Mechanisms; Opioids; Genetic; Neuroimaging; fMRI

资金

  1. National Institute of Health [R01-NS038145, R01-NS050578, R01-NS046694, R01-MH071260]
  2. General Clinical Research Center [RR-00095]
  3. NICHD [P30 HD15052]
  4. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [P30HD015052] Funding Source: NIH RePORTER
  5. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR000095] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH071260] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS046694, R01NS038145, R01NS050578] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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. (c) 2009 Elsevier Ltd. All rights reserved.

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