Ontogeny of respiratory sensitivity and tolerance to the mu-opioid agonist fentanyl in rat
Whereas developmental changes in analgesic sensitivity and tolerance to the mu-opioid agonist fentanyl have been reported, knowledge of respiratory responses to that drug is lacking. Using 7- and 14-day-old (P7, P14) and adult conscious rats, we first established, using whole body plethysmography, t...
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Veröffentlicht in: | Brain research. Developmental brain research 2005-05, Vol.156 (2), p.210-217 |
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description | Whereas developmental changes in analgesic sensitivity and tolerance to the mu-opioid agonist fentanyl have been reported, knowledge of respiratory responses to that drug is lacking. Using 7- and 14-day-old (P7, P14) and adult conscious rats, we first established, using whole body plethysmography, the fentanyl dose that decreased minute ventilation by 50% (ED50) at each age. ED50 increased with postnatal age (40, 60 and 120 μg/kg sc, respectively), indicating a high sensitivity to fentanyl in the youngest rats that decreased with maturation. In separate rat groups of the 3 ages, we injected each ED50 dose, once a day, for several consecutive days, until tolerance was established. Tolerance was defined as a reduction in respiratory depression from 50% to 75% of baseline. All age groups reached tolerance in minute ventilation, respiratory frequency, tidal volume and instantaneous flow (equivalent to respiratory drive). The P14 rat pups attained tolerance more rapidly (at 2.6 days) than did either the younger (5.1 days) or the adult rats (4.4 days). These results indicate that respiratory sensitivity and tolerance to fentanyl in rat vary in a distinct manner during maturation. |
doi_str_mv | 10.1016/j.devbrainres.2005.03.002 |
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Using 7- and 14-day-old (P7, P14) and adult conscious rats, we first established, using whole body plethysmography, the fentanyl dose that decreased minute ventilation by 50% (ED50) at each age. ED50 increased with postnatal age (40, 60 and 120 μg/kg sc, respectively), indicating a high sensitivity to fentanyl in the youngest rats that decreased with maturation. In separate rat groups of the 3 ages, we injected each ED50 dose, once a day, for several consecutive days, until tolerance was established. Tolerance was defined as a reduction in respiratory depression from 50% to 75% of baseline. All age groups reached tolerance in minute ventilation, respiratory frequency, tidal volume and instantaneous flow (equivalent to respiratory drive). The P14 rat pups attained tolerance more rapidly (at 2.6 days) than did either the younger (5.1 days) or the adult rats (4.4 days). These results indicate that respiratory sensitivity and tolerance to fentanyl in rat vary in a distinct manner during maturation.</description><identifier>ISSN: 0165-3806</identifier><identifier>DOI: 10.1016/j.devbrainres.2005.03.002</identifier><identifier>PMID: 16099308</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Age Factors ; Aging - drug effects ; Aging - physiology ; Analgesics, Opioid - adverse effects ; Analgesics, Opioid - pharmacology ; Analysis of Variance ; Animals ; Animals, Newborn ; Development ; Dose-Response Relationship, Drug ; Drug Tolerance - physiology ; Fentanyl ; Fentanyl - adverse effects ; Fentanyl - pharmacology ; Male ; Minute ventilation ; Plethysmography ; Plethysmography - methods ; Rat ; Rats ; Rats, Sprague-Dawley ; Receptors, Opioid, mu - agonists ; Respiration - drug effects ; Respiratory control ; Respiratory depression ; Respiratory Mechanics - drug effects ; Respiratory Mechanics - physiology ; Tidal Volume - drug effects ; Tidal Volume - physiology ; Time Factors</subject><ispartof>Brain research. Developmental brain research, 2005-05, Vol.156 (2), p.210-217</ispartof><rights>2005 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-986010854c85aa4e84a0cfc424b731a4aed11c419750bcfe94533df2935cb0703</citedby><cites>FETCH-LOGICAL-c488t-986010854c85aa4e84a0cfc424b731a4aed11c419750bcfe94533df2935cb0703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16099308$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Laferrière, Andrè</creatorcontrib><creatorcontrib>Colin-Durand, Jessica</creatorcontrib><creatorcontrib>Moss, Immanuela Ravè</creatorcontrib><title>Ontogeny of respiratory sensitivity and tolerance to the mu-opioid agonist fentanyl in rat</title><title>Brain research. Developmental brain research</title><addtitle>Brain Res Dev Brain Res</addtitle><description>Whereas developmental changes in analgesic sensitivity and tolerance to the mu-opioid agonist fentanyl have been reported, knowledge of respiratory responses to that drug is lacking. Using 7- and 14-day-old (P7, P14) and adult conscious rats, we first established, using whole body plethysmography, the fentanyl dose that decreased minute ventilation by 50% (ED50) at each age. ED50 increased with postnatal age (40, 60 and 120 μg/kg sc, respectively), indicating a high sensitivity to fentanyl in the youngest rats that decreased with maturation. In separate rat groups of the 3 ages, we injected each ED50 dose, once a day, for several consecutive days, until tolerance was established. Tolerance was defined as a reduction in respiratory depression from 50% to 75% of baseline. All age groups reached tolerance in minute ventilation, respiratory frequency, tidal volume and instantaneous flow (equivalent to respiratory drive). The P14 rat pups attained tolerance more rapidly (at 2.6 days) than did either the younger (5.1 days) or the adult rats (4.4 days). These results indicate that respiratory sensitivity and tolerance to fentanyl in rat vary in a distinct manner during maturation.</description><subject>Age Factors</subject><subject>Aging - drug effects</subject><subject>Aging - physiology</subject><subject>Analgesics, Opioid - adverse effects</subject><subject>Analgesics, Opioid - pharmacology</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Development</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Tolerance - physiology</subject><subject>Fentanyl</subject><subject>Fentanyl - adverse effects</subject><subject>Fentanyl - pharmacology</subject><subject>Male</subject><subject>Minute ventilation</subject><subject>Plethysmography</subject><subject>Plethysmography - methods</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Opioid, mu - agonists</subject><subject>Respiration - drug effects</subject><subject>Respiratory control</subject><subject>Respiratory depression</subject><subject>Respiratory Mechanics - drug effects</subject><subject>Respiratory Mechanics - physiology</subject><subject>Tidal Volume - drug effects</subject><subject>Tidal Volume - physiology</subject><subject>Time Factors</subject><issn>0165-3806</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtPwzAQhH0AUV5_AZkLt4R17DTOEVW8JCQucOFiOc6muErtYruV8u8xaiU4ctqVdmZW8xFyzaBkwOa3q7LHXRe0dQFjWQHUJfASoDoip_leF1zCfEbOYlwBAOOSnZAZm0PbcpCn5OPVJb9EN1E_0JywsUEnHyYa0UWb7M6miWrX0-RHDNoZzBtNn0jX28JvrLc91UvvbEx0QJe0m0ZqHc0pF-R40GPEy8M8J-8P92-Lp-Ll9fF5cfdSGCFlKlo5BwayFkbWWguUQoMZjKhE13CmhcaeMSNY29TQmQFbUXPeD1XLa9NBA_yc3OxzN8F_bTEmtbbR4Dhqh34bFWty6aZqsrDdC03wMQYc1CbYtQ6TYqB-YKqV-gNT_cBUwFWGmb1Xhyfbbo39r_NAMgsWewHmqjuLQUVjMfPqbUCTVO_tP958AxT0jyE</recordid><startdate>20050512</startdate><enddate>20050512</enddate><creator>Laferrière, Andrè</creator><creator>Colin-Durand, Jessica</creator><creator>Moss, Immanuela Ravè</creator><general>Elsevier B.V</general><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>20050512</creationdate><title>Ontogeny of respiratory sensitivity and tolerance to the mu-opioid agonist fentanyl in rat</title><author>Laferrière, Andrè ; Colin-Durand, Jessica ; Moss, Immanuela Ravè</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-986010854c85aa4e84a0cfc424b731a4aed11c419750bcfe94533df2935cb0703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age Factors</topic><topic>Aging - drug effects</topic><topic>Aging - physiology</topic><topic>Analgesics, Opioid - adverse effects</topic><topic>Analgesics, Opioid - pharmacology</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Development</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Tolerance - physiology</topic><topic>Fentanyl</topic><topic>Fentanyl - adverse effects</topic><topic>Fentanyl - pharmacology</topic><topic>Male</topic><topic>Minute ventilation</topic><topic>Plethysmography</topic><topic>Plethysmography - methods</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Opioid, mu - agonists</topic><topic>Respiration - drug effects</topic><topic>Respiratory control</topic><topic>Respiratory depression</topic><topic>Respiratory Mechanics - drug effects</topic><topic>Respiratory Mechanics - physiology</topic><topic>Tidal Volume - drug effects</topic><topic>Tidal Volume - physiology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laferrière, Andrè</creatorcontrib><creatorcontrib>Colin-Durand, Jessica</creatorcontrib><creatorcontrib>Moss, Immanuela Ravè</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Brain research. Developmental brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laferrière, Andrè</au><au>Colin-Durand, Jessica</au><au>Moss, Immanuela Ravè</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ontogeny of respiratory sensitivity and tolerance to the mu-opioid agonist fentanyl in rat</atitle><jtitle>Brain research. Developmental brain research</jtitle><addtitle>Brain Res Dev Brain Res</addtitle><date>2005-05-12</date><risdate>2005</risdate><volume>156</volume><issue>2</issue><spage>210</spage><epage>217</epage><pages>210-217</pages><issn>0165-3806</issn><abstract>Whereas developmental changes in analgesic sensitivity and tolerance to the mu-opioid agonist fentanyl have been reported, knowledge of respiratory responses to that drug is lacking. Using 7- and 14-day-old (P7, P14) and adult conscious rats, we first established, using whole body plethysmography, the fentanyl dose that decreased minute ventilation by 50% (ED50) at each age. ED50 increased with postnatal age (40, 60 and 120 μg/kg sc, respectively), indicating a high sensitivity to fentanyl in the youngest rats that decreased with maturation. In separate rat groups of the 3 ages, we injected each ED50 dose, once a day, for several consecutive days, until tolerance was established. Tolerance was defined as a reduction in respiratory depression from 50% to 75% of baseline. All age groups reached tolerance in minute ventilation, respiratory frequency, tidal volume and instantaneous flow (equivalent to respiratory drive). The P14 rat pups attained tolerance more rapidly (at 2.6 days) than did either the younger (5.1 days) or the adult rats (4.4 days). These results indicate that respiratory sensitivity and tolerance to fentanyl in rat vary in a distinct manner during maturation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>16099308</pmid><doi>10.1016/j.devbrainres.2005.03.002</doi><tpages>8</tpages></addata></record> |
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subjects | Age Factors Aging - drug effects Aging - physiology Analgesics, Opioid - adverse effects Analgesics, Opioid - pharmacology Analysis of Variance Animals Animals, Newborn Development Dose-Response Relationship, Drug Drug Tolerance - physiology Fentanyl Fentanyl - adverse effects Fentanyl - pharmacology Male Minute ventilation Plethysmography Plethysmography - methods Rat Rats Rats, Sprague-Dawley Receptors, Opioid, mu - agonists Respiration - drug effects Respiratory control Respiratory depression Respiratory Mechanics - drug effects Respiratory Mechanics - physiology Tidal Volume - drug effects Tidal Volume - physiology Time Factors |
title | Ontogeny of respiratory sensitivity and tolerance to the mu-opioid agonist fentanyl in rat |
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