The antinociceptive efficacy of morphine, metamizol, or their combination in an experimental rat model with different levels of inflammatory pain
The purpose of this work was to evaluate the antinociceptive efficacy of an optimal morphine and metamizol combination on different levels of nociception (levels I, II, and III) using the “Pain-induced functional impairment model in the rat”. The effect of acetylsalicylic acid was examined as a refe...
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Veröffentlicht in: | Pharmacology, biochemistry and behavior biochemistry and behavior, 2008-11, Vol.91 (1), p.196-201 |
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description | The purpose of this work was to evaluate the antinociceptive efficacy of an optimal morphine and metamizol combination on different levels of nociception (levels I, II, and III) using the “Pain-induced functional impairment model in the rat”. The effect of acetylsalicylic acid was examined as a reference drug at the same levels of nociception. The antinociceptive effects produced by morphine (3.2 mg/kg s.c.) and metamizol (177.8 mg/kg s.c.) were studied either individually or in combination. The antinociceptive efficacies were expressed as either areas under the curve (AUCs), maximum effects as functionality index in percent of the time course, or the antinociceptive effects produced at 2 h after administration. Unlike morphine, the antinociceptive effects of acetylsalicylic acid decreased with increasing intensity of nociception. In summary, the analysis of antinociceptive efficacies produced by the co-administration of these drugs for different levels of nociception revealed that co-administration provided potentiated and better antinociceptive coverage throughout our observation time than did the individual drugs or the expected theoretical sum (using AUC or effects after 2 h). This is the first study to demonstrate that an optimal morphine and metamizol combination is able to produce potentiation of antinociceptive effects during intense pain. |
doi_str_mv | 10.1016/j.pbb.2008.07.007 |
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The effect of acetylsalicylic acid was examined as a reference drug at the same levels of nociception. The antinociceptive effects produced by morphine (3.2 mg/kg s.c.) and metamizol (177.8 mg/kg s.c.) were studied either individually or in combination. The antinociceptive efficacies were expressed as either areas under the curve (AUCs), maximum effects as functionality index in percent of the time course, or the antinociceptive effects produced at 2 h after administration. Unlike morphine, the antinociceptive effects of acetylsalicylic acid decreased with increasing intensity of nociception. In summary, the analysis of antinociceptive efficacies produced by the co-administration of these drugs for different levels of nociception revealed that co-administration provided potentiated and better antinociceptive coverage throughout our observation time than did the individual drugs or the expected theoretical sum (using AUC or effects after 2 h). This is the first study to demonstrate that an optimal morphine and metamizol combination is able to produce potentiation of antinociceptive effects during intense pain.</description><identifier>ISSN: 0091-3057</identifier><identifier>EISSN: 1873-5177</identifier><identifier>DOI: 10.1016/j.pbb.2008.07.007</identifier><identifier>PMID: 18691611</identifier><identifier>CODEN: PBBHAU</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Analgesics, Opioid - therapeutic use ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Aspirin - therapeutic use ; Biological and medical sciences ; Dipyrone - therapeutic use ; Dose-Response Relationship, Drug ; Drug Synergism ; Drug Therapy, Combination ; Inflammation - chemically induced ; Inflammation - complications ; Male ; Medical sciences ; Metamizol ; Morphine ; Morphine - therapeutic use ; Nociception ; Pain ; Pain - chemically induced ; Pain - drug therapy ; Pain - etiology ; Pain Measurement - drug effects ; PIFIR model ; Rats ; Rats, Wistar ; Synergism ; Uric Acid</subject><ispartof>Pharmacology, biochemistry and behavior, 2008-11, Vol.91 (1), p.196-201</ispartof><rights>2008 Elsevier Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-f5f16d047d31671cdaf3eff6284068f443cc9007b9d7a922d49b85a3254e04013</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.pbb.2008.07.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20678595$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18691611$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LOPEZMUNOZ, F</creatorcontrib><creatorcontrib>GODINEZCHAPARRO, B</creatorcontrib><creatorcontrib>HUERTACRUZ, J</creatorcontrib><creatorcontrib>GUEVARALOPEZ, U</creatorcontrib><creatorcontrib>DOMINGUEZRAMIREZ, A</creatorcontrib><creatorcontrib>CORTESARROYO, A</creatorcontrib><title>The antinociceptive efficacy of morphine, metamizol, or their combination in an experimental rat model with different levels of inflammatory pain</title><title>Pharmacology, biochemistry and behavior</title><addtitle>Pharmacol Biochem Behav</addtitle><description>The purpose of this work was to evaluate the antinociceptive efficacy of an optimal morphine and metamizol combination on different levels of nociception (levels I, II, and III) using the “Pain-induced functional impairment model in the rat”. The effect of acetylsalicylic acid was examined as a reference drug at the same levels of nociception. The antinociceptive effects produced by morphine (3.2 mg/kg s.c.) and metamizol (177.8 mg/kg s.c.) were studied either individually or in combination. The antinociceptive efficacies were expressed as either areas under the curve (AUCs), maximum effects as functionality index in percent of the time course, or the antinociceptive effects produced at 2 h after administration. Unlike morphine, the antinociceptive effects of acetylsalicylic acid decreased with increasing intensity of nociception. In summary, the analysis of antinociceptive efficacies produced by the co-administration of these drugs for different levels of nociception revealed that co-administration provided potentiated and better antinociceptive coverage throughout our observation time than did the individual drugs or the expected theoretical sum (using AUC or effects after 2 h). This is the first study to demonstrate that an optimal morphine and metamizol combination is able to produce potentiation of antinociceptive effects during intense pain.</description><subject>Analgesics, Opioid - therapeutic use</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Aspirin - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Dipyrone - therapeutic use</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Synergism</subject><subject>Drug Therapy, Combination</subject><subject>Inflammation - chemically induced</subject><subject>Inflammation - complications</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metamizol</subject><subject>Morphine</subject><subject>Morphine - therapeutic use</subject><subject>Nociception</subject><subject>Pain</subject><subject>Pain - chemically induced</subject><subject>Pain - drug therapy</subject><subject>Pain - etiology</subject><subject>Pain Measurement - drug effects</subject><subject>PIFIR model</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Synergism</subject><subject>Uric Acid</subject><issn>0091-3057</issn><issn>1873-5177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kb2O1DAURiMEYmcXHoAGuYFqE64TJ05EhVb8SSvRLLXlONeaO0rsYHuGHd6CN8ajGUFH5cLnHl9_X1G84lBx4N27XbWOY1UD9BXICkA-KTa8l03ZcimfFhuAgZcNtPKquI5xBwCi7uTz4or33cA7zjfF74ctMu0SOW_I4JrogAytJaPNkXnLFh_WLTm8ZQsmvdAvP98yH1jaIgVm_DKS04m8Y-SyiOHjioEWdEnPLOiUBRPO7CelLZvIWgz5is14wDme_OTsrJdFJx-ObNXkXhTPrJ4jvrycN8X3Tx8f7r6U998-f737cF8awetU2tbybgIhp4Z3kptJ2ybv3dW9gK63QjTGDDmScZikHup6EsPYt7qpW4EggDc3xduzdw3-xx5jUgtFg_OsHfp9VHxoeyGgySA_gyb4GANateYP6nBUHNSpB7VTuQd16kGBVPnRPPP6It-PC07_Ji7BZ-DNBdDR6NkG7QzFv1wNnezboc3c-zOX48IDYVDREDqDEwU0SU2e_rPGH15Rp-g</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>LOPEZMUNOZ, F</creator><creator>GODINEZCHAPARRO, B</creator><creator>HUERTACRUZ, J</creator><creator>GUEVARALOPEZ, U</creator><creator>DOMINGUEZRAMIREZ, A</creator><creator>CORTESARROYO, A</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>7QG</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20081101</creationdate><title>The antinociceptive efficacy of morphine, metamizol, or their combination in an experimental rat model with different levels of inflammatory pain</title><author>LOPEZMUNOZ, F ; GODINEZCHAPARRO, B ; HUERTACRUZ, J ; GUEVARALOPEZ, U ; DOMINGUEZRAMIREZ, A ; CORTESARROYO, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-f5f16d047d31671cdaf3eff6284068f443cc9007b9d7a922d49b85a3254e04013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Analgesics, Opioid - therapeutic use</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Aspirin - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Dipyrone - therapeutic use</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Synergism</topic><topic>Drug Therapy, Combination</topic><topic>Inflammation - chemically induced</topic><topic>Inflammation - complications</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metamizol</topic><topic>Morphine</topic><topic>Morphine - therapeutic use</topic><topic>Nociception</topic><topic>Pain</topic><topic>Pain - chemically induced</topic><topic>Pain - drug therapy</topic><topic>Pain - etiology</topic><topic>Pain Measurement - drug effects</topic><topic>PIFIR model</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Synergism</topic><topic>Uric Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LOPEZMUNOZ, F</creatorcontrib><creatorcontrib>GODINEZCHAPARRO, B</creatorcontrib><creatorcontrib>HUERTACRUZ, J</creatorcontrib><creatorcontrib>GUEVARALOPEZ, U</creatorcontrib><creatorcontrib>DOMINGUEZRAMIREZ, A</creatorcontrib><creatorcontrib>CORTESARROYO, A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Pharmacology, biochemistry and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LOPEZMUNOZ, F</au><au>GODINEZCHAPARRO, B</au><au>HUERTACRUZ, J</au><au>GUEVARALOPEZ, U</au><au>DOMINGUEZRAMIREZ, A</au><au>CORTESARROYO, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The antinociceptive efficacy of morphine, metamizol, or their combination in an experimental rat model with different levels of inflammatory pain</atitle><jtitle>Pharmacology, biochemistry and behavior</jtitle><addtitle>Pharmacol Biochem Behav</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>91</volume><issue>1</issue><spage>196</spage><epage>201</epage><pages>196-201</pages><issn>0091-3057</issn><eissn>1873-5177</eissn><coden>PBBHAU</coden><abstract>The purpose of this work was to evaluate the antinociceptive efficacy of an optimal morphine and metamizol combination on different levels of nociception (levels I, II, and III) using the “Pain-induced functional impairment model in the rat”. The effect of acetylsalicylic acid was examined as a reference drug at the same levels of nociception. The antinociceptive effects produced by morphine (3.2 mg/kg s.c.) and metamizol (177.8 mg/kg s.c.) were studied either individually or in combination. The antinociceptive efficacies were expressed as either areas under the curve (AUCs), maximum effects as functionality index in percent of the time course, or the antinociceptive effects produced at 2 h after administration. Unlike morphine, the antinociceptive effects of acetylsalicylic acid decreased with increasing intensity of nociception. In summary, the analysis of antinociceptive efficacies produced by the co-administration of these drugs for different levels of nociception revealed that co-administration provided potentiated and better antinociceptive coverage throughout our observation time than did the individual drugs or the expected theoretical sum (using AUC or effects after 2 h). This is the first study to demonstrate that an optimal morphine and metamizol combination is able to produce potentiation of antinociceptive effects during intense pain.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18691611</pmid><doi>10.1016/j.pbb.2008.07.007</doi><tpages>6</tpages></addata></record> |
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subjects | Analgesics, Opioid - therapeutic use Animals Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Aspirin - therapeutic use Biological and medical sciences Dipyrone - therapeutic use Dose-Response Relationship, Drug Drug Synergism Drug Therapy, Combination Inflammation - chemically induced Inflammation - complications Male Medical sciences Metamizol Morphine Morphine - therapeutic use Nociception Pain Pain - chemically induced Pain - drug therapy Pain - etiology Pain Measurement - drug effects PIFIR model Rats Rats, Wistar Synergism Uric Acid |
title | The antinociceptive efficacy of morphine, metamizol, or their combination in an experimental rat model with different levels of inflammatory pain |
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