Anger regulation style, anger arousal and acute pain sensitivity: evidence for an endogenous opioid “triggering” model
Findings suggest that greater tendency to express anger is associated with greater sensitivity to acute pain via endogenous opioid system dysfunction, but past studies have not addressed the role of anger arousal. We used a 2 × 2 factorial design with Drug Condition (placebo or opioid blockade with...
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Veröffentlicht in: | Journal of behavioral medicine 2014-08, Vol.37 (4), p.642-653 |
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description | Findings suggest that greater tendency to express anger is associated with greater sensitivity to acute pain via endogenous opioid system dysfunction, but past studies have not addressed the role of anger arousal. We used a 2 × 2 factorial design with Drug Condition (placebo or opioid blockade with naltrexone) crossed with Task Order (anger-induction/pain-induction or pain-induction/anger-induction), and with continuous Anger-out Subscale scores. Drug × Task Order × Anger-out Subscale interactions were tested for pain intensity during a 4-min ischemic pain task performed by 146 healthy people. A significant Drug × Task Order × Anger-out Subscale interaction was dissected to reveal different patterns of pain intensity changes during the pain task for high anger-out participants who underwent pain-induction prior to anger-induction compared to those high in anger-out in the opposite order. Namely, when angered prior to pain, high anger-out participants appeared to exhibit low pain intensity under placebo that was not shown by high anger-out participants who received naltrexone. Results hint that people with a pronounced tendency to express anger may suffer from inadequate opioid function under simple pain-induction, but may experience analgesic benefit to some extent from the opioid triggering properties of strong anger arousal. |
doi_str_mv | 10.1007/s10865-013-9511-z |
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We used a 2 × 2 factorial design with Drug Condition (placebo or opioid blockade with naltrexone) crossed with Task Order (anger-induction/pain-induction or pain-induction/anger-induction), and with continuous Anger-out Subscale scores. Drug × Task Order × Anger-out Subscale interactions were tested for pain intensity during a 4-min ischemic pain task performed by 146 healthy people. A significant Drug × Task Order × Anger-out Subscale interaction was dissected to reveal different patterns of pain intensity changes during the pain task for high anger-out participants who underwent pain-induction prior to anger-induction compared to those high in anger-out in the opposite order. Namely, when angered prior to pain, high anger-out participants appeared to exhibit low pain intensity under placebo that was not shown by high anger-out participants who received naltrexone. Results hint that people with a pronounced tendency to express anger may suffer from inadequate opioid function under simple pain-induction, but may experience analgesic benefit to some extent from the opioid triggering properties of strong anger arousal.</description><identifier>ISSN: 0160-7715</identifier><identifier>EISSN: 1573-3521</identifier><identifier>DOI: 10.1007/s10865-013-9511-z</identifier><identifier>PMID: 23624641</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Acute pain ; Adult ; Analgesics ; Anger ; Anger - physiology ; Arousal - physiology ; Chronic pain ; Development and progression ; Diagnosis ; Double-Blind Method ; Family Medicine ; Female ; General Practice ; Health aspects ; Health Psychology ; Humans ; Male ; Medicine ; Medicine & Public Health ; Models, Biological ; Naltrexone - pharmacology ; Narcotic Antagonists - pharmacology ; Narcotics ; Opioid Peptides - antagonists & inhibitors ; Opioid Peptides - physiology ; Pain Measurement - drug effects ; Pain Threshold - drug effects ; Pain Threshold - physiology ; Pain Threshold - psychology ; Risk factors ; Young Adult</subject><ispartof>Journal of behavioral medicine, 2014-08, Vol.37 (4), p.642-653</ispartof><rights>Springer Science+Business Media New York 2013</rights><rights>COPYRIGHT 2014 Springer</rights><rights>Springer Science+Business Media New York 2014</rights><rights>Springer Science+Business Media New York 2013 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-g475t-1792d7a8c362b14f8e01de0790f9b3a1b710e4eee4d23de417ec97f99afda2793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10865-013-9511-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10865-013-9511-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,12826,27903,27904,30978,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23624641$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burns, John W.</creatorcontrib><creatorcontrib>Bruehl, Stephen</creatorcontrib><creatorcontrib>Chont, Melissa</creatorcontrib><title>Anger regulation style, anger arousal and acute pain sensitivity: evidence for an endogenous opioid “triggering” model</title><title>Journal of behavioral medicine</title><addtitle>J Behav Med</addtitle><addtitle>J Behav Med</addtitle><description>Findings suggest that greater tendency to express anger is associated with greater sensitivity to acute pain via endogenous opioid system dysfunction, but past studies have not addressed the role of anger arousal. We used a 2 × 2 factorial design with Drug Condition (placebo or opioid blockade with naltrexone) crossed with Task Order (anger-induction/pain-induction or pain-induction/anger-induction), and with continuous Anger-out Subscale scores. Drug × Task Order × Anger-out Subscale interactions were tested for pain intensity during a 4-min ischemic pain task performed by 146 healthy people. A significant Drug × Task Order × Anger-out Subscale interaction was dissected to reveal different patterns of pain intensity changes during the pain task for high anger-out participants who underwent pain-induction prior to anger-induction compared to those high in anger-out in the opposite order. Namely, when angered prior to pain, high anger-out participants appeared to exhibit low pain intensity under placebo that was not shown by high anger-out participants who received naltrexone. Results hint that people with a pronounced tendency to express anger may suffer from inadequate opioid function under simple pain-induction, but may experience analgesic benefit to some extent from the opioid triggering properties of strong anger arousal.</description><subject>Acute pain</subject><subject>Adult</subject><subject>Analgesics</subject><subject>Anger</subject><subject>Anger - physiology</subject><subject>Arousal - physiology</subject><subject>Chronic pain</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Double-Blind Method</subject><subject>Family Medicine</subject><subject>Female</subject><subject>General Practice</subject><subject>Health aspects</subject><subject>Health Psychology</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Models, Biological</subject><subject>Naltrexone - pharmacology</subject><subject>Narcotic Antagonists - pharmacology</subject><subject>Narcotics</subject><subject>Opioid Peptides - antagonists & inhibitors</subject><subject>Opioid Peptides - physiology</subject><subject>Pain Measurement - drug effects</subject><subject>Pain Threshold - drug effects</subject><subject>Pain Threshold - physiology</subject><subject>Pain Threshold - psychology</subject><subject>Risk factors</subject><subject>Young Adult</subject><issn>0160-7715</issn><issn>1573-3521</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptksFu1DAQhi0EokvhAbggS1yb4omdOOaAtKqAVqrEBc6WN54EV4m92MlKu6c-CLxcnwQvW6CVVj5YHn_ze8bzE_Ia2DkwJt8lYE1dFQx4oSqAYveELKCSvOBVCU_JgkHNCimhOiEvUrphjNVKqOfkpOR1KWoBC7Jb-h4jjdjPg5lc8DRN2wHPqPkTNzHMyQz5ZKlp5wnp2rjMoE9uchs3bd9T3DiLvkXahZzgKXobevQ5kYa1C87Su9ufU3R9FnS-v7v9RcdgcXhJnnVmSPjqfj8l3z59_HpxWVx_-Xx1sbwueiGrqQCpSitN0-aaVyC6BhlYZFKxTq24gZUEhgIRhS25RQESWyU7pUxnTSkVPyUfDrrreTWibdFP0Qx6Hd1o4lYH4_TjG---6z5stICGAfAs8PZeIIYfM6ZJ34Q5-lyzhkpwxpuylv-p3gyone9CFmtHl1q95A3jogTeZKo4QuXvwvxy8Ni5HH7Enx_h87I4uvZowpuH3f5r8-_IM1AegLTejwPjg26Y3vtKH3yls6_03ld6x38DA7HBUw</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Burns, John W.</creator><creator>Bruehl, Stephen</creator><creator>Chont, Melissa</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>0-V</scope><scope>3V.</scope><scope>7QJ</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HEHIP</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20140801</creationdate><title>Anger regulation style, anger arousal and acute pain sensitivity: evidence for an endogenous opioid “triggering” model</title><author>Burns, John W. ; Bruehl, Stephen ; Chont, Melissa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g475t-1792d7a8c362b14f8e01de0790f9b3a1b710e4eee4d23de417ec97f99afda2793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acute pain</topic><topic>Adult</topic><topic>Analgesics</topic><topic>Anger</topic><topic>Anger - physiology</topic><topic>Arousal - physiology</topic><topic>Chronic pain</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Double-Blind Method</topic><topic>Family Medicine</topic><topic>Female</topic><topic>General Practice</topic><topic>Health aspects</topic><topic>Health Psychology</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Models, Biological</topic><topic>Naltrexone - pharmacology</topic><topic>Narcotic Antagonists - pharmacology</topic><topic>Narcotics</topic><topic>Opioid Peptides - antagonists & inhibitors</topic><topic>Opioid Peptides - physiology</topic><topic>Pain Measurement - drug effects</topic><topic>Pain Threshold - drug effects</topic><topic>Pain Threshold - physiology</topic><topic>Pain Threshold - psychology</topic><topic>Risk factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burns, John W.</creatorcontrib><creatorcontrib>Bruehl, Stephen</creatorcontrib><creatorcontrib>Chont, Melissa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Sociology Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Sociology Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of behavioral medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burns, John W.</au><au>Bruehl, Stephen</au><au>Chont, Melissa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anger regulation style, anger arousal and acute pain sensitivity: evidence for an endogenous opioid “triggering” model</atitle><jtitle>Journal of behavioral medicine</jtitle><stitle>J Behav Med</stitle><addtitle>J Behav Med</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>37</volume><issue>4</issue><spage>642</spage><epage>653</epage><pages>642-653</pages><issn>0160-7715</issn><eissn>1573-3521</eissn><abstract>Findings suggest that greater tendency to express anger is associated with greater sensitivity to acute pain via endogenous opioid system dysfunction, but past studies have not addressed the role of anger arousal. We used a 2 × 2 factorial design with Drug Condition (placebo or opioid blockade with naltrexone) crossed with Task Order (anger-induction/pain-induction or pain-induction/anger-induction), and with continuous Anger-out Subscale scores. Drug × Task Order × Anger-out Subscale interactions were tested for pain intensity during a 4-min ischemic pain task performed by 146 healthy people. A significant Drug × Task Order × Anger-out Subscale interaction was dissected to reveal different patterns of pain intensity changes during the pain task for high anger-out participants who underwent pain-induction prior to anger-induction compared to those high in anger-out in the opposite order. Namely, when angered prior to pain, high anger-out participants appeared to exhibit low pain intensity under placebo that was not shown by high anger-out participants who received naltrexone. Results hint that people with a pronounced tendency to express anger may suffer from inadequate opioid function under simple pain-induction, but may experience analgesic benefit to some extent from the opioid triggering properties of strong anger arousal.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>23624641</pmid><doi>10.1007/s10865-013-9511-z</doi><tpages>12</tpages></addata></record> |
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subjects | Acute pain Adult Analgesics Anger Anger - physiology Arousal - physiology Chronic pain Development and progression Diagnosis Double-Blind Method Family Medicine Female General Practice Health aspects Health Psychology Humans Male Medicine Medicine & Public Health Models, Biological Naltrexone - pharmacology Narcotic Antagonists - pharmacology Narcotics Opioid Peptides - antagonists & inhibitors Opioid Peptides - physiology Pain Measurement - drug effects Pain Threshold - drug effects Pain Threshold - physiology Pain Threshold - psychology Risk factors Young Adult |
title | Anger regulation style, anger arousal and acute pain sensitivity: evidence for an endogenous opioid “triggering” model |
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