Reduction of Pulmonary Edema by Short-Acting Local Anesthetics
Local anesthetics (LAs) possess a variety of effects that cannot be explained by the typical block of neuronal sodium channels. Antithrombotic effects of LAs are well known, but LAs also act as bactericides. Therefore, an investigation of the influence of LAs on the inflammatory response of the isol...
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creator | Konrad, Christoph J. Schuepfer, Guido K. Neuburger, Michael Schley, Marcus Schmelz, Martin Schmeck, Joachim |
description | Local anesthetics (LAs) possess a variety of effects that cannot be explained by the typical block of neuronal sodium channels. Antithrombotic effects of LAs are well known, but LAs also act as bactericides. Therefore, an investigation of the influence of LAs on the inflammatory response of the isolated rat lung (n = 78) to an
N-formyl-
l-leucin-methionyl-
l-phenylalanine (FMLP) stimulus was performed.
The experiments were performed on isolated and ventilated rat lungs perfused with cell-free and plasma-free buffer. LAs (lidocaine and mepivacaine) were injected in various concentrations before application and activation of human granulocytes by FMLP. Pulmonary arterial pressure (PAP) and lung weight gain were monitored continuously. LAs in final dosages from 10
−2 to 10
−7 mg/kg body weight (n = 6 each) were injected into the pulmonary artery before treatment with FMLP (10
−6 M) to induce pulmonary arterial hypertension. Perfusate samples were taken intermittently to determine thromboxane A
2 (TX A
2) and endothelin-1 concentrations. Microscopic analyses were performed to assess the degree of lung injury.
Pretreatment with LAs significantly reduced the FMLP-induced PAP increase (treatment group
v sham group: 0.5 to 5 mm Hg
v 8 mm Hg;
P < .05) and the release of endothelin-1 (2.4
v 5 fmol/mL). Histologic damage seen as acute granulocytic alveolitis was reduced by lidocaine and mepivacaine, even below clinically relevant concentrations.
LA pretreatment reduces inflammatory reactions after FMLP stimulus. |
doi_str_mv | 10.1016/j.rapm.2006.01.003 |
format | Article |
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N-formyl-
l-leucin-methionyl-
l-phenylalanine (FMLP) stimulus was performed.
The experiments were performed on isolated and ventilated rat lungs perfused with cell-free and plasma-free buffer. LAs (lidocaine and mepivacaine) were injected in various concentrations before application and activation of human granulocytes by FMLP. Pulmonary arterial pressure (PAP) and lung weight gain were monitored continuously. LAs in final dosages from 10
−2 to 10
−7 mg/kg body weight (n = 6 each) were injected into the pulmonary artery before treatment with FMLP (10
−6 M) to induce pulmonary arterial hypertension. Perfusate samples were taken intermittently to determine thromboxane A
2 (TX A
2) and endothelin-1 concentrations. Microscopic analyses were performed to assess the degree of lung injury.
Pretreatment with LAs significantly reduced the FMLP-induced PAP increase (treatment group
v sham group: 0.5 to 5 mm Hg
v 8 mm Hg;
P < .05) and the release of endothelin-1 (2.4
v 5 fmol/mL). Histologic damage seen as acute granulocytic alveolitis was reduced by lidocaine and mepivacaine, even below clinically relevant concentrations.
LA pretreatment reduces inflammatory reactions after FMLP stimulus.</description><identifier>ISSN: 1098-7339</identifier><identifier>EISSN: 1532-8651</identifier><identifier>DOI: 10.1016/j.rapm.2006.01.003</identifier><identifier>PMID: 16701192</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Anesthetics, Local - pharmacology ; Anesthetics, Local - therapeutic use ; Animals ; Blood Pressure ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Endothelin ; FMLP ; Granulocytes - drug effects ; Granulocytes - pathology ; In Vitro Techniques ; Lidocaine - pharmacology ; Lidocaine - therapeutic use ; Local anesthetics ; Lung ; Lung - blood supply ; Lung - drug effects ; Lung - pathology ; Mepivacaine - pharmacology ; Mepivacaine - therapeutic use ; N-Formylmethionine Leucyl-Phenylalanine ; Organ Size ; Pneumonia - chemically induced ; Pneumonia - drug therapy ; Pneumonia - pathology ; Pulmonary Artery - drug effects ; Pulmonary Artery - physiopathology ; Pulmonary Edema - chemically induced ; Pulmonary Edema - drug therapy ; Pulmonary Edema - pathology ; Rats ; Rats, Sprague-Dawley ; Regional anesthesia ; Time Factors</subject><ispartof>Regional anesthesia and pain medicine, 2006-05, Vol.31 (3), p.254-259</ispartof><rights>2006 American Society of Regional Anesthesia and Pain Medicine</rights><rights>Copyright Churchill Livingstone Inc., Medical Publishers May/Jun 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-9c128ae009dc3e13d9a718418c4e189d7428e1408b86da3f4e995409465e7b7e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16701192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Konrad, Christoph J.</creatorcontrib><creatorcontrib>Schuepfer, Guido K.</creatorcontrib><creatorcontrib>Neuburger, Michael</creatorcontrib><creatorcontrib>Schley, Marcus</creatorcontrib><creatorcontrib>Schmelz, Martin</creatorcontrib><creatorcontrib>Schmeck, Joachim</creatorcontrib><title>Reduction of Pulmonary Edema by Short-Acting Local Anesthetics</title><title>Regional anesthesia and pain medicine</title><addtitle>Reg Anesth Pain Med</addtitle><description>Local anesthetics (LAs) possess a variety of effects that cannot be explained by the typical block of neuronal sodium channels. Antithrombotic effects of LAs are well known, but LAs also act as bactericides. Therefore, an investigation of the influence of LAs on the inflammatory response of the isolated rat lung (n = 78) to an
N-formyl-
l-leucin-methionyl-
l-phenylalanine (FMLP) stimulus was performed.
The experiments were performed on isolated and ventilated rat lungs perfused with cell-free and plasma-free buffer. LAs (lidocaine and mepivacaine) were injected in various concentrations before application and activation of human granulocytes by FMLP. Pulmonary arterial pressure (PAP) and lung weight gain were monitored continuously. LAs in final dosages from 10
−2 to 10
−7 mg/kg body weight (n = 6 each) were injected into the pulmonary artery before treatment with FMLP (10
−6 M) to induce pulmonary arterial hypertension. Perfusate samples were taken intermittently to determine thromboxane A
2 (TX A
2) and endothelin-1 concentrations. Microscopic analyses were performed to assess the degree of lung injury.
Pretreatment with LAs significantly reduced the FMLP-induced PAP increase (treatment group
v sham group: 0.5 to 5 mm Hg
v 8 mm Hg;
P < .05) and the release of endothelin-1 (2.4
v 5 fmol/mL). Histologic damage seen as acute granulocytic alveolitis was reduced by lidocaine and mepivacaine, even below clinically relevant concentrations.
LA pretreatment reduces inflammatory reactions after FMLP stimulus.</description><subject>Anesthetics, Local - pharmacology</subject><subject>Anesthetics, Local - therapeutic use</subject><subject>Animals</subject><subject>Blood Pressure</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endothelin</subject><subject>FMLP</subject><subject>Granulocytes - drug effects</subject><subject>Granulocytes - pathology</subject><subject>In Vitro Techniques</subject><subject>Lidocaine - pharmacology</subject><subject>Lidocaine - therapeutic use</subject><subject>Local anesthetics</subject><subject>Lung</subject><subject>Lung - blood supply</subject><subject>Lung - drug effects</subject><subject>Lung - pathology</subject><subject>Mepivacaine - pharmacology</subject><subject>Mepivacaine - therapeutic use</subject><subject>N-Formylmethionine Leucyl-Phenylalanine</subject><subject>Organ Size</subject><subject>Pneumonia - chemically induced</subject><subject>Pneumonia - drug therapy</subject><subject>Pneumonia - pathology</subject><subject>Pulmonary Artery - drug effects</subject><subject>Pulmonary Artery - physiopathology</subject><subject>Pulmonary Edema - chemically induced</subject><subject>Pulmonary Edema - drug therapy</subject><subject>Pulmonary Edema - pathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regional anesthesia</subject><subject>Time Factors</subject><issn>1098-7339</issn><issn>1532-8651</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE1Lw0AQhhdRrFb_gAcJ3hNnsptkF0QopX5AQfHjvCS7U5vSZOsmEfrv3dKCN08zh-d9h3kYu0JIEDC_XSW-3DRJCpAngAkAP2JnmPE0lnmGx2EHJeOCczVi5123AgBZiPyUjTAvAFGlZ-z-jexg-tq1kVtEr8O6cW3pt9HMUlNG1TZ6Xzrfx5OAtF_R3JlyHU1a6vol9bXpLtjJolx3dHmYY_b5MPuYPsXzl8fn6WQeGy6xj5XBVJYEoKzhhNyqskApUBpBKJUtRCoJBchK5rbkC0FKZQKUyDMqqoL4mN3sezfefQ_hvF65wbfhpE4hw1QUPAtQuoeMd13naaE3vm7CNxpB74zpld4Z0ztjGlAHYyF0fWgeqobsX-SgKAB3e4DCfz81ed2ZmlpDtvZkem1d_V__L3-Meok</recordid><startdate>20060501</startdate><enddate>20060501</enddate><creator>Konrad, Christoph J.</creator><creator>Schuepfer, Guido K.</creator><creator>Neuburger, Michael</creator><creator>Schley, Marcus</creator><creator>Schmelz, Martin</creator><creator>Schmeck, Joachim</creator><general>Elsevier Inc</general><general>BMJ Publishing Group LTD</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20060501</creationdate><title>Reduction of Pulmonary Edema by Short-Acting Local Anesthetics</title><author>Konrad, Christoph J. ; Schuepfer, Guido K. ; Neuburger, Michael ; Schley, Marcus ; Schmelz, Martin ; Schmeck, Joachim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-9c128ae009dc3e13d9a718418c4e189d7428e1408b86da3f4e995409465e7b7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Anesthetics, Local - pharmacology</topic><topic>Anesthetics, Local - therapeutic use</topic><topic>Animals</topic><topic>Blood Pressure</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endothelin</topic><topic>FMLP</topic><topic>Granulocytes - drug effects</topic><topic>Granulocytes - pathology</topic><topic>In Vitro Techniques</topic><topic>Lidocaine - pharmacology</topic><topic>Lidocaine - therapeutic use</topic><topic>Local anesthetics</topic><topic>Lung</topic><topic>Lung - blood supply</topic><topic>Lung - drug effects</topic><topic>Lung - pathology</topic><topic>Mepivacaine - pharmacology</topic><topic>Mepivacaine - therapeutic use</topic><topic>N-Formylmethionine Leucyl-Phenylalanine</topic><topic>Organ Size</topic><topic>Pneumonia - chemically induced</topic><topic>Pneumonia - drug therapy</topic><topic>Pneumonia - pathology</topic><topic>Pulmonary Artery - drug effects</topic><topic>Pulmonary Artery - physiopathology</topic><topic>Pulmonary Edema - chemically induced</topic><topic>Pulmonary Edema - drug therapy</topic><topic>Pulmonary Edema - pathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regional anesthesia</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Konrad, Christoph J.</creatorcontrib><creatorcontrib>Schuepfer, Guido K.</creatorcontrib><creatorcontrib>Neuburger, Michael</creatorcontrib><creatorcontrib>Schley, Marcus</creatorcontrib><creatorcontrib>Schmelz, Martin</creatorcontrib><creatorcontrib>Schmeck, Joachim</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>Regional anesthesia and pain medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konrad, Christoph J.</au><au>Schuepfer, Guido K.</au><au>Neuburger, Michael</au><au>Schley, Marcus</au><au>Schmelz, Martin</au><au>Schmeck, Joachim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduction of Pulmonary Edema by Short-Acting Local Anesthetics</atitle><jtitle>Regional anesthesia and pain medicine</jtitle><addtitle>Reg Anesth Pain Med</addtitle><date>2006-05-01</date><risdate>2006</risdate><volume>31</volume><issue>3</issue><spage>254</spage><epage>259</epage><pages>254-259</pages><issn>1098-7339</issn><eissn>1532-8651</eissn><abstract>Local anesthetics (LAs) possess a variety of effects that cannot be explained by the typical block of neuronal sodium channels. Antithrombotic effects of LAs are well known, but LAs also act as bactericides. Therefore, an investigation of the influence of LAs on the inflammatory response of the isolated rat lung (n = 78) to an
N-formyl-
l-leucin-methionyl-
l-phenylalanine (FMLP) stimulus was performed.
The experiments were performed on isolated and ventilated rat lungs perfused with cell-free and plasma-free buffer. LAs (lidocaine and mepivacaine) were injected in various concentrations before application and activation of human granulocytes by FMLP. Pulmonary arterial pressure (PAP) and lung weight gain were monitored continuously. LAs in final dosages from 10
−2 to 10
−7 mg/kg body weight (n = 6 each) were injected into the pulmonary artery before treatment with FMLP (10
−6 M) to induce pulmonary arterial hypertension. Perfusate samples were taken intermittently to determine thromboxane A
2 (TX A
2) and endothelin-1 concentrations. Microscopic analyses were performed to assess the degree of lung injury.
Pretreatment with LAs significantly reduced the FMLP-induced PAP increase (treatment group
v sham group: 0.5 to 5 mm Hg
v 8 mm Hg;
P < .05) and the release of endothelin-1 (2.4
v 5 fmol/mL). Histologic damage seen as acute granulocytic alveolitis was reduced by lidocaine and mepivacaine, even below clinically relevant concentrations.
LA pretreatment reduces inflammatory reactions after FMLP stimulus.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>16701192</pmid><doi>10.1016/j.rapm.2006.01.003</doi><tpages>6</tpages></addata></record> |
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subjects | Anesthetics, Local - pharmacology Anesthetics, Local - therapeutic use Animals Blood Pressure Disease Models, Animal Dose-Response Relationship, Drug Endothelin FMLP Granulocytes - drug effects Granulocytes - pathology In Vitro Techniques Lidocaine - pharmacology Lidocaine - therapeutic use Local anesthetics Lung Lung - blood supply Lung - drug effects Lung - pathology Mepivacaine - pharmacology Mepivacaine - therapeutic use N-Formylmethionine Leucyl-Phenylalanine Organ Size Pneumonia - chemically induced Pneumonia - drug therapy Pneumonia - pathology Pulmonary Artery - drug effects Pulmonary Artery - physiopathology Pulmonary Edema - chemically induced Pulmonary Edema - drug therapy Pulmonary Edema - pathology Rats Rats, Sprague-Dawley Regional anesthesia Time Factors |
title | Reduction of Pulmonary Edema by Short-Acting Local Anesthetics |
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