Buprenorphine Treatment of Opiate and Cocaine Abuse: Clinical and Preclinical Studies
Buprenorphine, an opioid mixed agonist-antagonist, is a potent analgesic that appears to be effective for the treatment of opiate abuse. Recent preclinical studies have shown that buprenorphine also significantly reduces cocaine self-administration by rhesus monkeys for periods up to 120 days. This...
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Veröffentlicht in: | Harvard review of psychiatry 1993-09, Vol.1 (3), p.168-183 |
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description | Buprenorphine, an opioid mixed agonist-antagonist, is a potent analgesic that appears to be effective for the treatment of opiate abuse. Recent preclinical studies have shown that buprenorphine also significantly reduces cocaine self-administration by rhesus monkeys for periods up to 120 days. This unexpected finding has led to clinical trials to evaluate buprenorphine's effectiveness for the treatment of dependence on both cocaine and opiates, as defined by DSM-III-R criteria. Buprenorphine's safety in combination with cocaine and opiates and its effects on electroencephalographic sleep patterns and regional cerebral blood flow were evaluated during inpatient studies. Buprenorphine (4 or 8 mg/day given sublingually) did not accentuate the cardiovascular and respiratory changes induced by an acute challenge dose of cocaine (30 mg given intravenously) or morphine (10 mg given intravenously) alone. In an outpatient open trial, buprenorphine significantly reduced both opiate and cocaine abuse by patients who had abused these drugs for more than 10 years. Most of these patients had failed in other drug abuse treatment programs. Reports of needle sharing also decreased significantly, and no patient tested positive for human Immunodeficiency virus (HIV). The apparent safety and effectiveness of buprenorphine, combined with a high level of patient acceptance, led the Food and Drug Administration to grant a compassionate extension of the approved period for outpatient buprenorphine treatment from 26 to 52 weeks. Clinical trials of buprenorphine are ongoing. Possible mechanisms underlying buprenorphine-cocaine interactions are now under investigation. |
doi_str_mv | 10.3109/10673229309017075 |
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Leonard</creator><creatorcontrib>Mello, Nancy K. ; Mendelson, Jack H. ; Lukas, Scott E. ; Gastfriend, David R. ; Teoh, Siew Koon ; Holman, B. Leonard</creatorcontrib><description>Buprenorphine, an opioid mixed agonist-antagonist, is a potent analgesic that appears to be effective for the treatment of opiate abuse. Recent preclinical studies have shown that buprenorphine also significantly reduces cocaine self-administration by rhesus monkeys for periods up to 120 days. This unexpected finding has led to clinical trials to evaluate buprenorphine's effectiveness for the treatment of dependence on both cocaine and opiates, as defined by DSM-III-R criteria. Buprenorphine's safety in combination with cocaine and opiates and its effects on electroencephalographic sleep patterns and regional cerebral blood flow were evaluated during inpatient studies. Buprenorphine (4 or 8 mg/day given sublingually) did not accentuate the cardiovascular and respiratory changes induced by an acute challenge dose of cocaine (30 mg given intravenously) or morphine (10 mg given intravenously) alone. In an outpatient open trial, buprenorphine significantly reduced both opiate and cocaine abuse by patients who had abused these drugs for more than 10 years. Most of these patients had failed in other drug abuse treatment programs. Reports of needle sharing also decreased significantly, and no patient tested positive for human Immunodeficiency virus (HIV). The apparent safety and effectiveness of buprenorphine, combined with a high level of patient acceptance, led the Food and Drug Administration to grant a compassionate extension of the approved period for outpatient buprenorphine treatment from 26 to 52 weeks. Clinical trials of buprenorphine are ongoing. Possible mechanisms underlying buprenorphine-cocaine interactions are now under investigation.</description><identifier>ISSN: 1067-3229</identifier><identifier>EISSN: 1465-7309</identifier><identifier>DOI: 10.3109/10673229309017075</identifier><identifier>PMID: 9384844</identifier><language>eng</language><publisher>United States: Informa UK Ltd</publisher><subject>Animals ; Buprenorphine - adverse effects ; Buprenorphine - therapeutic use ; Clinical Trials as Topic ; Cocaine-Related Disorders - psychology ; Cocaine-Related Disorders - rehabilitation ; Drug Evaluation, Preclinical ; Drug Interactions ; Humans ; Macaca mulatta ; Opioid-Related Disorders - psychology ; Opioid-Related Disorders - rehabilitation ; Treatment Outcome</subject><ispartof>Harvard review of psychiatry, 1993-09, Vol.1 (3), p.168-183</ispartof><rights>1993 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1993</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-ebf35514164579959cc3978bd53a62fa908a2e44dd7658f2ca59d102665509663</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/10673229309017075$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/10673229309017075$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,61194,61375</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9384844$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mello, Nancy K.</creatorcontrib><creatorcontrib>Mendelson, Jack H.</creatorcontrib><creatorcontrib>Lukas, Scott E.</creatorcontrib><creatorcontrib>Gastfriend, David R.</creatorcontrib><creatorcontrib>Teoh, Siew Koon</creatorcontrib><creatorcontrib>Holman, B. Leonard</creatorcontrib><title>Buprenorphine Treatment of Opiate and Cocaine Abuse: Clinical and Preclinical Studies</title><title>Harvard review of psychiatry</title><addtitle>Harv Rev Psychiatry</addtitle><description>Buprenorphine, an opioid mixed agonist-antagonist, is a potent analgesic that appears to be effective for the treatment of opiate abuse. Recent preclinical studies have shown that buprenorphine also significantly reduces cocaine self-administration by rhesus monkeys for periods up to 120 days. This unexpected finding has led to clinical trials to evaluate buprenorphine's effectiveness for the treatment of dependence on both cocaine and opiates, as defined by DSM-III-R criteria. Buprenorphine's safety in combination with cocaine and opiates and its effects on electroencephalographic sleep patterns and regional cerebral blood flow were evaluated during inpatient studies. Buprenorphine (4 or 8 mg/day given sublingually) did not accentuate the cardiovascular and respiratory changes induced by an acute challenge dose of cocaine (30 mg given intravenously) or morphine (10 mg given intravenously) alone. In an outpatient open trial, buprenorphine significantly reduced both opiate and cocaine abuse by patients who had abused these drugs for more than 10 years. Most of these patients had failed in other drug abuse treatment programs. Reports of needle sharing also decreased significantly, and no patient tested positive for human Immunodeficiency virus (HIV). The apparent safety and effectiveness of buprenorphine, combined with a high level of patient acceptance, led the Food and Drug Administration to grant a compassionate extension of the approved period for outpatient buprenorphine treatment from 26 to 52 weeks. Clinical trials of buprenorphine are ongoing. Possible mechanisms underlying buprenorphine-cocaine interactions are now under investigation.</description><subject>Animals</subject><subject>Buprenorphine - adverse effects</subject><subject>Buprenorphine - therapeutic use</subject><subject>Clinical Trials as Topic</subject><subject>Cocaine-Related Disorders - psychology</subject><subject>Cocaine-Related Disorders - rehabilitation</subject><subject>Drug Evaluation, Preclinical</subject><subject>Drug Interactions</subject><subject>Humans</subject><subject>Macaca mulatta</subject><subject>Opioid-Related Disorders - psychology</subject><subject>Opioid-Related Disorders - rehabilitation</subject><subject>Treatment Outcome</subject><issn>1067-3229</issn><issn>1465-7309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKw0AUhgdRaq0-gAshLxCd-2R0VYM3KFSwXYfJzAlNyY2ZZOHbm5rqRnB1Lt_5fzg_QtcE3zKC9R3BUjFKNcMaE4WVOEFzwqWI1bg5HfuRx4eDc3QRwh5jrCmmMzTTLOEJ53O0fRw6D03ru13ZQLTxYPoamj5qi2jdlaaHyDQuSltrDnyZDwHuo7Qqm9Ka6pu9e7A_80c_uBLCJTorTBXg6lgXaPv8tElf49X65S1drmLLFOtjyAsmBOFEcqG0FtpaplWSO8GMpIXRODEUOHdOSZEU1BqhHcFUSiGwlpItEJl8rW9D8FBknS9r4z8zgrNDQtmfhEbNzaTphrwG96s4RjLyh4mXTdH62uzAVP3OGg_Zvh18M_7zj_sXa6ByEg</recordid><startdate>19930901</startdate><enddate>19930901</enddate><creator>Mello, Nancy K.</creator><creator>Mendelson, Jack H.</creator><creator>Lukas, Scott E.</creator><creator>Gastfriend, David R.</creator><creator>Teoh, Siew Koon</creator><creator>Holman, B. 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Leonard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-ebf35514164579959cc3978bd53a62fa908a2e44dd7658f2ca59d102665509663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Buprenorphine - adverse effects</topic><topic>Buprenorphine - therapeutic use</topic><topic>Clinical Trials as Topic</topic><topic>Cocaine-Related Disorders - psychology</topic><topic>Cocaine-Related Disorders - rehabilitation</topic><topic>Drug Evaluation, Preclinical</topic><topic>Drug Interactions</topic><topic>Humans</topic><topic>Macaca mulatta</topic><topic>Opioid-Related Disorders - psychology</topic><topic>Opioid-Related Disorders - rehabilitation</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mello, Nancy K.</creatorcontrib><creatorcontrib>Mendelson, Jack H.</creatorcontrib><creatorcontrib>Lukas, Scott E.</creatorcontrib><creatorcontrib>Gastfriend, David R.</creatorcontrib><creatorcontrib>Teoh, Siew Koon</creatorcontrib><creatorcontrib>Holman, B. 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Leonard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Buprenorphine Treatment of Opiate and Cocaine Abuse: Clinical and Preclinical Studies</atitle><jtitle>Harvard review of psychiatry</jtitle><addtitle>Harv Rev Psychiatry</addtitle><date>1993-09-01</date><risdate>1993</risdate><volume>1</volume><issue>3</issue><spage>168</spage><epage>183</epage><pages>168-183</pages><issn>1067-3229</issn><eissn>1465-7309</eissn><abstract>Buprenorphine, an opioid mixed agonist-antagonist, is a potent analgesic that appears to be effective for the treatment of opiate abuse. Recent preclinical studies have shown that buprenorphine also significantly reduces cocaine self-administration by rhesus monkeys for periods up to 120 days. This unexpected finding has led to clinical trials to evaluate buprenorphine's effectiveness for the treatment of dependence on both cocaine and opiates, as defined by DSM-III-R criteria. Buprenorphine's safety in combination with cocaine and opiates and its effects on electroencephalographic sleep patterns and regional cerebral blood flow were evaluated during inpatient studies. Buprenorphine (4 or 8 mg/day given sublingually) did not accentuate the cardiovascular and respiratory changes induced by an acute challenge dose of cocaine (30 mg given intravenously) or morphine (10 mg given intravenously) alone. In an outpatient open trial, buprenorphine significantly reduced both opiate and cocaine abuse by patients who had abused these drugs for more than 10 years. Most of these patients had failed in other drug abuse treatment programs. Reports of needle sharing also decreased significantly, and no patient tested positive for human Immunodeficiency virus (HIV). 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subjects | Animals Buprenorphine - adverse effects Buprenorphine - therapeutic use Clinical Trials as Topic Cocaine-Related Disorders - psychology Cocaine-Related Disorders - rehabilitation Drug Evaluation, Preclinical Drug Interactions Humans Macaca mulatta Opioid-Related Disorders - psychology Opioid-Related Disorders - rehabilitation Treatment Outcome |
title | Buprenorphine Treatment of Opiate and Cocaine Abuse: Clinical and Preclinical Studies |
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