Relative Involvement of Spinal Opioid Receptors in Physical Dependence on Intrathecal Butorphanol and Morphine

The present study was carried out to investigate the relative involvement of spinal opioid receptors in the development of physical dependence on intrathecal (IT) butorphanol in comparison with IT morphine. Dependence was induced by continuous IT infusion of butorphanol (52 nmol/h) and morphine (26...

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Veröffentlicht in:Pharmacology, biochemistry and behavior biochemistry and behavior, 1998-08, Vol.60 (4), p.899-907
Hauptverfasser: Wongchanapai, W., Tsang, B.K., He, Z., Ho, I.K.
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container_issue 4
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container_title Pharmacology, biochemistry and behavior
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creator Wongchanapai, W.
Tsang, B.K.
He, Z.
Ho, I.K.
description The present study was carried out to investigate the relative involvement of spinal opioid receptors in the development of physical dependence on intrathecal (IT) butorphanol in comparison with IT morphine. Dependence was induced by continuous IT infusion of butorphanol (52 nmol/h) and morphine (26 nmol/h) for 4 days in male Sprague–Dawley rats. Naloxone, CTOP, naltrindole, and nor-binaltorphimine (nor-BNI) were administered IT to precipitate behavioral signs of withdrawal. Administration of IT naloxone produced a significantly greater increase in the profile of withdrawal signs in IT morphine dependence than that in IT butorphanol dependence. An IT nor-BNI challenge elicits behavioral signs of withdrawal only in rats dependent on IT butorphanol, but not in rats dependent on IT morphine. CTOP administered IT precipitated withdrawal signs in IT morphine dependence that were greater than that in IT butorphanol dependence. An IT treatment with naltrindole produced equivalent signs of withdrawal in both IT butorphanol- and morphine-dependent rats. These results suggest that continuous IT butorphanol results in the development of less physical dependence than that of IT morphine. Spinal κ- rather than δ- and μ-opioid receptors play a major role in the development of IT butorphanol dependence, whereas spinal μ-opioid receptors play a more important role than δ-opioid receptors in IT morphine dependence.
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Dependence was induced by continuous IT infusion of butorphanol (52 nmol/h) and morphine (26 nmol/h) for 4 days in male Sprague–Dawley rats. Naloxone, CTOP, naltrindole, and nor-binaltorphimine (nor-BNI) were administered IT to precipitate behavioral signs of withdrawal. Administration of IT naloxone produced a significantly greater increase in the profile of withdrawal signs in IT morphine dependence than that in IT butorphanol dependence. An IT nor-BNI challenge elicits behavioral signs of withdrawal only in rats dependent on IT butorphanol, but not in rats dependent on IT morphine. CTOP administered IT precipitated withdrawal signs in IT morphine dependence that were greater than that in IT butorphanol dependence. An IT treatment with naltrindole produced equivalent signs of withdrawal in both IT butorphanol- and morphine-dependent rats. These results suggest that continuous IT butorphanol results in the development of less physical dependence than that of IT morphine. Spinal κ- rather than δ- and μ-opioid receptors play a major role in the development of IT butorphanol dependence, whereas spinal μ-opioid receptors play a more important role than δ-opioid receptors in IT morphine dependence.</description><identifier>ISSN: 0091-3057</identifier><identifier>EISSN: 1873-5177</identifier><identifier>DOI: 10.1016/S0091-3057(98)00074-4</identifier><identifier>PMID: 9700974</identifier><identifier>CODEN: PBBHAU</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Butorphanol ; Butorphanol - administration &amp; dosage ; Drug toxicity and drugs side effects treatment ; Injections, Spinal ; Intrathecal ; Male ; Medical sciences ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Morphine ; Morphine - administration &amp; dosage ; Morphine Dependence - physiopathology ; Narcotic Antagonists - administration &amp; dosage ; Narcotic Antagonists - pharmacology ; Narcotics - administration &amp; dosage ; Opioid-Related Disorders - physiopathology ; Pharmacology. 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Dependence was induced by continuous IT infusion of butorphanol (52 nmol/h) and morphine (26 nmol/h) for 4 days in male Sprague–Dawley rats. Naloxone, CTOP, naltrindole, and nor-binaltorphimine (nor-BNI) were administered IT to precipitate behavioral signs of withdrawal. Administration of IT naloxone produced a significantly greater increase in the profile of withdrawal signs in IT morphine dependence than that in IT butorphanol dependence. An IT nor-BNI challenge elicits behavioral signs of withdrawal only in rats dependent on IT butorphanol, but not in rats dependent on IT morphine. CTOP administered IT precipitated withdrawal signs in IT morphine dependence that were greater than that in IT butorphanol dependence. An IT treatment with naltrindole produced equivalent signs of withdrawal in both IT butorphanol- and morphine-dependent rats. These results suggest that continuous IT butorphanol results in the development of less physical dependence than that of IT morphine. Spinal κ- rather than δ- and μ-opioid receptors play a major role in the development of IT butorphanol dependence, whereas spinal μ-opioid receptors play a more important role than δ-opioid receptors in IT morphine dependence.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Butorphanol</subject><subject>Butorphanol - administration &amp; dosage</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Injections, Spinal</subject><subject>Intrathecal</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Morphine</subject><subject>Morphine - administration &amp; dosage</subject><subject>Morphine Dependence - physiopathology</subject><subject>Narcotic Antagonists - administration &amp; dosage</subject><subject>Narcotic Antagonists - pharmacology</subject><subject>Narcotics - administration &amp; dosage</subject><subject>Opioid-Related Disorders - physiopathology</subject><subject>Pharmacology. Drug treatments</subject><subject>Physical dependence</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Opioid - drug effects</subject><subject>Spinal Cord - physiology</subject><subject>Substance Withdrawal Syndrome - psychology</subject><issn>0091-3057</issn><issn>1873-5177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1rFDEUQIModa3-hEIeRPRh2mQz-XoSrR8ttFRafQ7Z5IaNzCbTZHah_95Md9lXn0I4596Eg9AZJeeUUHHxQIimHSNcftTqEyFE9l3_Ai2okqzjVMqXaHFUXqM3tf5tUr8U8gSdaNmQ7Bco3cNgp7gDfJ12edjBBtKEc8APY0x2wHdjzNHje3AwTrlUHBP-tX6q0TX4DUZIHpIDnFNbMBU7rWEmX7dNHtc25QHb5PHtfIsJ3qJXwQ4V3h3OU_Tnx_ffl1fdzd3P68svN53rlZi6oLQLLOggLeGccLXqlYKgKfNMauidZERIwu3Kc0Ws8IJbLpijKxCEa85O0Yf93rHkxy3UyWxidTAMNkHeVkOl4JwK3US-F13JtRYIZixxY8uTocTMnc1zZzNHNFqZ586mb3Nnhwe2qw3449QhbOPvD9zWFiQUm1ysR23JFKV02bTPew1ajF2EYqqLc1AfC7jJ-Bz_85F_JyiaSw</recordid><startdate>19980801</startdate><enddate>19980801</enddate><creator>Wongchanapai, W.</creator><creator>Tsang, B.K.</creator><creator>He, Z.</creator><creator>Ho, I.K.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>19980801</creationdate><title>Relative Involvement of Spinal Opioid Receptors in Physical Dependence on Intrathecal Butorphanol and Morphine</title><author>Wongchanapai, W. ; Tsang, B.K. ; He, Z. ; Ho, I.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-f89cf3f9f7a055058b488ef913d379e4c7306705abd580a6d65a563c1be605953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Butorphanol</topic><topic>Butorphanol - administration &amp; dosage</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Injections, Spinal</topic><topic>Intrathecal</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Morphine</topic><topic>Morphine - administration &amp; dosage</topic><topic>Morphine Dependence - physiopathology</topic><topic>Narcotic Antagonists - administration &amp; dosage</topic><topic>Narcotic Antagonists - pharmacology</topic><topic>Narcotics - administration &amp; dosage</topic><topic>Opioid-Related Disorders - physiopathology</topic><topic>Pharmacology. 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subjects Animals
Biological and medical sciences
Butorphanol
Butorphanol - administration & dosage
Drug toxicity and drugs side effects treatment
Injections, Spinal
Intrathecal
Male
Medical sciences
Miscellaneous (drug allergy, mutagens, teratogens...)
Morphine
Morphine - administration & dosage
Morphine Dependence - physiopathology
Narcotic Antagonists - administration & dosage
Narcotic Antagonists - pharmacology
Narcotics - administration & dosage
Opioid-Related Disorders - physiopathology
Pharmacology. Drug treatments
Physical dependence
Rats
Rats, Sprague-Dawley
Receptors, Opioid - drug effects
Spinal Cord - physiology
Substance Withdrawal Syndrome - psychology
title Relative Involvement of Spinal Opioid Receptors in Physical Dependence on Intrathecal Butorphanol and Morphine
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