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However, little is known about what resting plasma <jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content> levels might reveal about functioning of the endogenous opioid antinociceptive system. This study directly examined associations between resting plasma <jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content> and subsequent endogenous opioid analgesic responses to acute pain in 39 healthy controls and 37 individuals with chronic low back pain (<jats:styled-content style=\"fixed-case\">LBP<\/jats:styled-content>). Resting baseline levels of plasma <jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content> were assessed. Next, participants received opioid blockade (8\u2009mg naloxone i.v.) or placebo in a double\u2010blind, randomized, crossover design. Participants then underwent two acute pain stimuli: finger pressure (<jats:styled-content style=\"fixed-case\">FP<\/jats:styled-content>) pain and ischaemic (<jats:styled-content style=\"fixed-case\">ISC<\/jats:styled-content>) forearm pain. Blockade effects (naloxone minus placebo pain ratings) were derived to index endogenous opioid analgesic function. In placebo condition analyses for both pain stimuli, higher resting <jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content> levels were associated with subsequently greater reported pain intensity (<jats:styled-content style=\"fixed-case\"><jats:italic>p<\/jats:italic>'s<\/jats:styled-content>\u2009&lt;\u20090.05), with this effect occurring primarily in healthy controls (<jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content>\u2009\u00d7\u2009<jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>articipant <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>ype interactions, <jats:styled-content style=\"fixed-case\"><jats:italic>p<\/jats:italic>'s<\/jats:styled-content>\u2009&lt;\u20090.05). In blockade effect analyses across both pain tasks, higher resting plasma <jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content> predicted less subsequent endogenous opioid analgesia (smaller blockade effects; <jats:styled-content style=\"fixed-case\"><jats:italic>p<\/jats:italic>'s<\/jats:styled-content>\u2009&lt;\u20090.05). For the <jats:styled-content style=\"fixed-case\">ISC<\/jats:styled-content> task, these links were significantly more prominent in <jats:styled-content style=\"fixed-case\">LBP<\/jats:styled-content> participants (<jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content>\u2009\u00d7\u2009<jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>articipant <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>ype <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>nteractions, <jats:styled-content style=\"fixed-case\"><jats:italic>p<\/jats:italic>'s<\/jats:styled-content>\u2009&lt;\u20090.05). Results suggest that elevated resting plasma <jats:styled-content style=\"fixed-case\">BE<\/jats:styled-content> may be a potential biomarker for reduced endogenous opioid analgesic capacity, particularly among individuals with chronic pain. Potential clinical implications are discussed.<\/jats:p>","DOI":"10.1002\/j.1532-2149.2011.00021.x","type":"journal-article","created":{"date-parts":[[2011,12,22]],"date-time":"2011-12-22T11:38:15Z","timestamp":1324553895000},"page":"370-380","source":"Crossref","is-referenced-by-count":48,"title":["What do plasma beta\u2010endorphin levels reveal about endogenous opioid analgesic function?"],"prefix":"10.1002","volume":"16","author":[{"given":"S.","family":"Bruehl","sequence":"first","affiliation":[{"name":"Department of Anesthesiology Vanderbilt University School of Medicine  Nashville TN USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.W.","family":"Burns","sequence":"additional","affiliation":[{"name":"Department of Behavioral Science Rush University  Chicago IL USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O.Y.","family":"Chung","sequence":"additional","affiliation":[{"name":"Department of Anesthesiology Vanderbilt University School of 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