Pharmacokinetics Do Not Explain the Absence of an Anesthetic Effect of Perfluoropropane or Perfluoropentane
In conflict with the prediction of the Meyer-Overton hypothesis, perfluoropropane (C,F,) and perfluoropentane (C5F12) have no anesthetic effect in rats. To test whether this resulted from a failure of the inspired drugs to reach the brain, we determined the increase in partial pressures of C,F, and...
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Veröffentlicht in: | Anesthesia and analgesia 1994-08, Vol.79 (2), p.234-237 |
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creator | Chortkoff, Ben S. Laster, Michael J. Koblin, Donald D. Taheri, Shahram Eger, Edmond I Halsey, Michael J. |
description | In conflict with the prediction of the Meyer-Overton hypothesis, perfluoropropane (C,F,) and perfluoropentane (C5F12) have no anesthetic effect in rats. To test whether this resulted from a failure of the inspired drugs to reach the brain, we determined the increase in partial pressures of C,F, and C,F, in the blood and brains of rats exposed to 0.65 ata of each drug. C3F8 and C5F12 blood/gas partition coefficients equaled 0.00125 ± 0.00037 (mean plusmn; SD, n = 9) and 0.00277 plusmn; 0.00082 (n = 4), and brain/gas partition coefficients equaled 0.0119 plusmn; 0.0002 (n = 4) and 0.0229 plusmn; 0.0055 (n = 7), respectively. As a fraction of the inspired value (Pa/PI), the partial pressures of C3F8 and C5F12 in blood (Pa) were 0.99 ±0.12 and 0.69 plusmn; 0.19, respectively, 30 min after administration. The increases in cerebral (Pb) partial pressures of both drugs paralleled the arterial increases (Pb/PI = 0.85 plusmn; 0.02, and 1.05 plusmn; 0.03, respectively at 30 min), with C3F8 reaching a plateau at 2 h of 96% ± 4% of the partial pressure of inspired gas. We conclude that failure of C3F8 and C5F12, to reach the brain does not account for the absence of an anesthetic effect of these compounds. |
doi_str_mv | 10.1213/00000539-199408000-00005 |
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To test whether this resulted from a failure of the inspired drugs to reach the brain, we determined the increase in partial pressures of C,F, and C,F, in the blood and brains of rats exposed to 0.65 ata of each drug. C3F8 and C5F12 blood/gas partition coefficients equaled 0.00125 ± 0.00037 (mean plusmn; SD, n = 9) and 0.00277 plusmn; 0.00082 (n = 4), and brain/gas partition coefficients equaled 0.0119 plusmn; 0.0002 (n = 4) and 0.0229 plusmn; 0.0055 (n = 7), respectively. As a fraction of the inspired value (Pa/PI), the partial pressures of C3F8 and C5F12 in blood (Pa) were 0.99 ±0.12 and 0.69 plusmn; 0.19, respectively, 30 min after administration. The increases in cerebral (Pb) partial pressures of both drugs paralleled the arterial increases (Pb/PI = 0.85 plusmn; 0.02, and 1.05 plusmn; 0.03, respectively at 30 min), with C3F8 reaching a plateau at 2 h of 96% ± 4% of the partial pressure of inspired gas. We conclude that failure of C3F8 and C5F12, to reach the brain does not account for the absence of an anesthetic effect of these compounds.</description><identifier>ISSN: 0003-2999</identifier><identifier>EISSN: 1526-7598</identifier><identifier>DOI: 10.1213/00000539-199408000-00005</identifier><identifier>PMID: 7639356</identifier><identifier>CODEN: AACRAT</identifier><language>eng</language><publisher>Hagerstown, MD: International Anesthesia Research Society</publisher><subject>Anesthesia, Inhalation ; Anesthetics. Neuromuscular blocking agents ; Animals ; Biological and medical sciences ; Blood-Brain Barrier - drug effects ; Brain - metabolism ; Fluorocarbons - pharmacokinetics ; Fluorocarbons - pharmacology ; Male ; Medical sciences ; Neuropharmacology ; Pharmacology. Drug treatments ; Rats ; Rats, Sprague-Dawley ; Specific Pathogen-Free Organisms</subject><ispartof>Anesthesia and analgesia, 1994-08, Vol.79 (2), p.234-237</ispartof><rights>1994 International Anesthesia Research Society</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4345-547cc4fe647ab1fd9248e0ee30bee69afa935ec40658c57b6c8bd6031ed485133</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf><![CDATA[$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&PDF=y&D=ovft&AN=00000539-199408000-00005$$EPDF$$P50$$Gwolterskluwer$$H]]></linktopdf><linktohtml>$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00000539-199408000-00005$$EHTML$$P50$$Gwolterskluwer$$H</linktohtml><link.rule.ids>314,780,784,4609,27924,27925,64666,65461</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4235772$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7639356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chortkoff, Ben S.</creatorcontrib><creatorcontrib>Laster, Michael J.</creatorcontrib><creatorcontrib>Koblin, Donald D.</creatorcontrib><creatorcontrib>Taheri, Shahram</creatorcontrib><creatorcontrib>Eger, Edmond I</creatorcontrib><creatorcontrib>Halsey, Michael J.</creatorcontrib><title>Pharmacokinetics Do Not Explain the Absence of an Anesthetic Effect of Perfluoropropane or Perfluoropentane</title><title>Anesthesia and analgesia</title><addtitle>Anesth Analg</addtitle><description>In conflict with the prediction of the Meyer-Overton hypothesis, perfluoropropane (C,F,) and perfluoropentane (C5F12) have no anesthetic effect in rats. To test whether this resulted from a failure of the inspired drugs to reach the brain, we determined the increase in partial pressures of C,F, and C,F, in the blood and brains of rats exposed to 0.65 ata of each drug. C3F8 and C5F12 blood/gas partition coefficients equaled 0.00125 ± 0.00037 (mean plusmn; SD, n = 9) and 0.00277 plusmn; 0.00082 (n = 4), and brain/gas partition coefficients equaled 0.0119 plusmn; 0.0002 (n = 4) and 0.0229 plusmn; 0.0055 (n = 7), respectively. As a fraction of the inspired value (Pa/PI), the partial pressures of C3F8 and C5F12 in blood (Pa) were 0.99 ±0.12 and 0.69 plusmn; 0.19, respectively, 30 min after administration. The increases in cerebral (Pb) partial pressures of both drugs paralleled the arterial increases (Pb/PI = 0.85 plusmn; 0.02, and 1.05 plusmn; 0.03, respectively at 30 min), with C3F8 reaching a plateau at 2 h of 96% ± 4% of the partial pressure of inspired gas. We conclude that failure of C3F8 and C5F12, to reach the brain does not account for the absence of an anesthetic effect of these compounds.</description><subject>Anesthesia, Inhalation</subject><subject>Anesthetics. Neuromuscular blocking agents</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood-Brain Barrier - drug effects</subject><subject>Brain - metabolism</subject><subject>Fluorocarbons - pharmacokinetics</subject><subject>Fluorocarbons - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Specific Pathogen-Free Organisms</subject><issn>0003-2999</issn><issn>1526-7598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1uGyEUhVHUyHWdPEIkFlV308LwNyyt1EkrRYkXyRox-CJPjQcXZuT07YNj1-qmCAnd754LRweEMCVfaU3ZN3JYgumKas1JU4rqnVygKRW1rJTQzQc0LYhVtdb6I_qU869SUtLICZooyTQTcoo2y7VNW-viputh6FzG3yN-jANevO6C7Xo8rAHP2wy9Axw9tj2e95ALLWK88B7ccOBLSD6MMcVd2bYv2vQPg34o7ApdehsyXJ_OGXq5Wzzf_qgenu5_3s4fKscZF5XgyjnuQXJlW-pXuuYNEABGWgCprbfFOjhOpGicUK10TbuShFFY8UZQxmboy_He4uX3WMyabZcdhFA8xDEbpSilgtMibI5Cl2LOCbzZpW5r0x9DiTnkbP7mbM45myOZoZvTG2O7hdV58BRs6X8-9W12Nvhke9fls4zXTChVFxk_yvYxDJDyJox7SGYNNgxr879fZm_tO5W5</recordid><startdate>199408</startdate><enddate>199408</enddate><creator>Chortkoff, Ben S.</creator><creator>Laster, Michael J.</creator><creator>Koblin, Donald D.</creator><creator>Taheri, Shahram</creator><creator>Eger, Edmond I</creator><creator>Halsey, Michael J.</creator><general>International Anesthesia Research Society</general><general>Lippincott</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>7X8</scope></search><sort><creationdate>199408</creationdate><title>Pharmacokinetics Do Not Explain the Absence of an Anesthetic Effect of Perfluoropropane or Perfluoropentane</title><author>Chortkoff, Ben S. ; Laster, Michael J. ; Koblin, Donald D. ; Taheri, Shahram ; Eger, Edmond I ; Halsey, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4345-547cc4fe647ab1fd9248e0ee30bee69afa935ec40658c57b6c8bd6031ed485133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Anesthesia, Inhalation</topic><topic>Anesthetics. Neuromuscular blocking agents</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood-Brain Barrier - drug effects</topic><topic>Brain - metabolism</topic><topic>Fluorocarbons - pharmacokinetics</topic><topic>Fluorocarbons - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Specific Pathogen-Free Organisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chortkoff, Ben S.</creatorcontrib><creatorcontrib>Laster, Michael J.</creatorcontrib><creatorcontrib>Koblin, Donald D.</creatorcontrib><creatorcontrib>Taheri, Shahram</creatorcontrib><creatorcontrib>Eger, Edmond I</creatorcontrib><creatorcontrib>Halsey, Michael J.</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>MEDLINE - Academic</collection><jtitle>Anesthesia and analgesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chortkoff, Ben S.</au><au>Laster, Michael J.</au><au>Koblin, Donald D.</au><au>Taheri, Shahram</au><au>Eger, Edmond I</au><au>Halsey, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics Do Not Explain the Absence of an Anesthetic Effect of Perfluoropropane or Perfluoropentane</atitle><jtitle>Anesthesia and analgesia</jtitle><addtitle>Anesth Analg</addtitle><date>1994-08</date><risdate>1994</risdate><volume>79</volume><issue>2</issue><spage>234</spage><epage>237</epage><pages>234-237</pages><issn>0003-2999</issn><eissn>1526-7598</eissn><coden>AACRAT</coden><abstract>In conflict with the prediction of the Meyer-Overton hypothesis, perfluoropropane (C,F,) and perfluoropentane (C5F12) have no anesthetic effect in rats. To test whether this resulted from a failure of the inspired drugs to reach the brain, we determined the increase in partial pressures of C,F, and C,F, in the blood and brains of rats exposed to 0.65 ata of each drug. C3F8 and C5F12 blood/gas partition coefficients equaled 0.00125 ± 0.00037 (mean plusmn; SD, n = 9) and 0.00277 plusmn; 0.00082 (n = 4), and brain/gas partition coefficients equaled 0.0119 plusmn; 0.0002 (n = 4) and 0.0229 plusmn; 0.0055 (n = 7), respectively. As a fraction of the inspired value (Pa/PI), the partial pressures of C3F8 and C5F12 in blood (Pa) were 0.99 ±0.12 and 0.69 plusmn; 0.19, respectively, 30 min after administration. The increases in cerebral (Pb) partial pressures of both drugs paralleled the arterial increases (Pb/PI = 0.85 plusmn; 0.02, and 1.05 plusmn; 0.03, respectively at 30 min), with C3F8 reaching a plateau at 2 h of 96% ± 4% of the partial pressure of inspired gas. We conclude that failure of C3F8 and C5F12, to reach the brain does not account for the absence of an anesthetic effect of these compounds.</abstract><cop>Hagerstown, MD</cop><pub>International Anesthesia Research Society</pub><pmid>7639356</pmid><doi>10.1213/00000539-199408000-00005</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia, Inhalation Anesthetics. Neuromuscular blocking agents Animals Biological and medical sciences Blood-Brain Barrier - drug effects Brain - metabolism Fluorocarbons - pharmacokinetics Fluorocarbons - pharmacology Male Medical sciences Neuropharmacology Pharmacology. Drug treatments Rats Rats, Sprague-Dawley Specific Pathogen-Free Organisms |
title | Pharmacokinetics Do Not Explain the Absence of an Anesthetic Effect of Perfluoropropane or Perfluoropentane |
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