Recruitment maneuver in pulmonary and extrapulmonary experimental acute lung injury
OBJECTIVE:The aim of this study is to test the hypothesis that recruitment maneuvers (RMs) might act differently in models of pulmonary (p) and extrapulmonary (exp) acute lung injury (ALI) with similar transpulmonary pressure changes. DESIGN:Prospective, randomized, controlled experimental study. SE...
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creator | Riva, Douglas R Oliveira, Mariana B. G Rzezinski, Andréia F Rangel, Graziela Capelozzi, Vera L Zin, Walter A Morales, Marcelo M Pelosi, Paolo Rocco, Patricia R. M |
description | OBJECTIVE:The aim of this study is to test the hypothesis that recruitment maneuvers (RMs) might act differently in models of pulmonary (p) and extrapulmonary (exp) acute lung injury (ALI) with similar transpulmonary pressure changes.
DESIGN:Prospective, randomized, controlled experimental study.
SETTING:University research laboratory.
SUBJECTS:Wistar rats were randomly divided into four groups. In control groups, sterile saline solution was intratracheally (0.1 mL, Cp) or intraperitoneally (1 mL, Cexp) injected, whereas ALI animals received Escherichia coli lipopolysaccharide intratracheally (100 μg, ALIp) or intraperitoneally (1 mg, ALIexp). After 24 hrs, animals were mechanically ventilated (tidal volume, 6 mL/kg; positive end-expiratory pressure, 5 cm H2O) and three RMs (pressure inflations to 40 cm H2O for 40 secs, 1 min apart) applied.
MEASUREMENTS AND MAIN RESULTS:Pao2, lung resistive and viscoelastic pressures, static elastance, lung histology (light and electron microscopy), and type III procollagen messenger RNA expression in pulmonary tissue were measured before RMs and at the end of 1 hr of mechanical ventilation. Mechanical variables, gas exchange, and the fraction of area of alveolar collapse were similar in both ALI groups. After RMs, lung resistive and viscoelastic pressures and static elastance decreased more in ALIexp (255%, 180%, and 118%, respectively) than in ALIp (103%, 59%, and 89%, respectively). The amount of atelectasis decreased more in ALIexp than in ALIp (from 58% to 19% and from 59% to 33%, respectively). RMs augmented type III procollagen messenger RNA expression only in the ALIp group (19%), associated with worsening in alveolar epithelium injury but no capillary endothelium lesion, whereas the ALIexp group showed a minor detachment of the alveolar capillary membrane.
CONCLUSIONS:Given the same transpulmonary pressures, RMs are more effective at opening collapsed alveoli in ALIexp than in ALIp, thus improving lung mechanics and oxygenation with limited damage to alveolar epithelium. |
doi_str_mv | 10.1097/CCM.0b013e3181760e5d |
format | Article |
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DESIGN:Prospective, randomized, controlled experimental study.
SETTING:University research laboratory.
SUBJECTS:Wistar rats were randomly divided into four groups. In control groups, sterile saline solution was intratracheally (0.1 mL, Cp) or intraperitoneally (1 mL, Cexp) injected, whereas ALI animals received Escherichia coli lipopolysaccharide intratracheally (100 μg, ALIp) or intraperitoneally (1 mg, ALIexp). After 24 hrs, animals were mechanically ventilated (tidal volume, 6 mL/kg; positive end-expiratory pressure, 5 cm H2O) and three RMs (pressure inflations to 40 cm H2O for 40 secs, 1 min apart) applied.
MEASUREMENTS AND MAIN RESULTS:Pao2, lung resistive and viscoelastic pressures, static elastance, lung histology (light and electron microscopy), and type III procollagen messenger RNA expression in pulmonary tissue were measured before RMs and at the end of 1 hr of mechanical ventilation. Mechanical variables, gas exchange, and the fraction of area of alveolar collapse were similar in both ALI groups. After RMs, lung resistive and viscoelastic pressures and static elastance decreased more in ALIexp (255%, 180%, and 118%, respectively) than in ALIp (103%, 59%, and 89%, respectively). The amount of atelectasis decreased more in ALIexp than in ALIp (from 58% to 19% and from 59% to 33%, respectively). RMs augmented type III procollagen messenger RNA expression only in the ALIp group (19%), associated with worsening in alveolar epithelium injury but no capillary endothelium lesion, whereas the ALIexp group showed a minor detachment of the alveolar capillary membrane.
CONCLUSIONS:Given the same transpulmonary pressures, RMs are more effective at opening collapsed alveoli in ALIexp than in ALIp, thus improving lung mechanics and oxygenation with limited damage to alveolar epithelium.</description><identifier>ISSN: 0090-3493</identifier><identifier>EISSN: 1530-0293</identifier><identifier>DOI: 10.1097/CCM.0b013e3181760e5d</identifier><identifier>PMID: 18496360</identifier><identifier>CODEN: CCMDC7</identifier><language>eng</language><publisher>Hagerstown, MD: by the Society of Critical Care Medicine and Lippincott Williams & Wilkins</publisher><subject>Airway Resistance - physiology ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Capillary Permeability - physiology ; Collagen Type III - genetics ; Disease Models, Animal ; Endothelium, Vascular - pathology ; Endothelium, Vascular - physiopathology ; Gene Expression - physiology ; Intensive care medicine ; Lung Compliance - physiology ; Medical sciences ; Microscopy, Electron ; Oxygen - blood ; Pneumology ; Pulmonary Alveoli - blood supply ; Pulmonary Alveoli - pathology ; Pulmonary Alveoli - physiopathology ; Pulmonary Atelectasis - pathology ; Pulmonary Atelectasis - physiopathology ; Pulmonary Gas Exchange - physiology ; Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases ; Rats ; Rats, Wistar ; Respiratory Distress Syndrome, Adult - pathology ; Respiratory Distress Syndrome, Adult - physiopathology ; Respiratory Mechanics - physiology ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; Systemic Inflammatory Response Syndrome - pathology ; Systemic Inflammatory Response Syndrome - physiopathology</subject><ispartof>Critical care medicine, 2008-06, Vol.36 (6), p.1900-1908</ispartof><rights>2008 by the Society of Critical Care Medicine and Lippincott Williams & Wilkins</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384d-931455ac5f0a09083014dfbb0b6196074c591ba80aa9fca5baf64d9c2b24ec873</citedby><cites>FETCH-LOGICAL-c384d-931455ac5f0a09083014dfbb0b6196074c591ba80aa9fca5baf64d9c2b24ec873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20388594$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18496360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Riva, Douglas R</creatorcontrib><creatorcontrib>Oliveira, Mariana B. G</creatorcontrib><creatorcontrib>Rzezinski, Andréia F</creatorcontrib><creatorcontrib>Rangel, Graziela</creatorcontrib><creatorcontrib>Capelozzi, Vera L</creatorcontrib><creatorcontrib>Zin, Walter A</creatorcontrib><creatorcontrib>Morales, Marcelo M</creatorcontrib><creatorcontrib>Pelosi, Paolo</creatorcontrib><creatorcontrib>Rocco, Patricia R. M</creatorcontrib><title>Recruitment maneuver in pulmonary and extrapulmonary experimental acute lung injury</title><title>Critical care medicine</title><addtitle>Crit Care Med</addtitle><description>OBJECTIVE:The aim of this study is to test the hypothesis that recruitment maneuvers (RMs) might act differently in models of pulmonary (p) and extrapulmonary (exp) acute lung injury (ALI) with similar transpulmonary pressure changes.
DESIGN:Prospective, randomized, controlled experimental study.
SETTING:University research laboratory.
SUBJECTS:Wistar rats were randomly divided into four groups. In control groups, sterile saline solution was intratracheally (0.1 mL, Cp) or intraperitoneally (1 mL, Cexp) injected, whereas ALI animals received Escherichia coli lipopolysaccharide intratracheally (100 μg, ALIp) or intraperitoneally (1 mg, ALIexp). After 24 hrs, animals were mechanically ventilated (tidal volume, 6 mL/kg; positive end-expiratory pressure, 5 cm H2O) and three RMs (pressure inflations to 40 cm H2O for 40 secs, 1 min apart) applied.
MEASUREMENTS AND MAIN RESULTS:Pao2, lung resistive and viscoelastic pressures, static elastance, lung histology (light and electron microscopy), and type III procollagen messenger RNA expression in pulmonary tissue were measured before RMs and at the end of 1 hr of mechanical ventilation. Mechanical variables, gas exchange, and the fraction of area of alveolar collapse were similar in both ALI groups. After RMs, lung resistive and viscoelastic pressures and static elastance decreased more in ALIexp (255%, 180%, and 118%, respectively) than in ALIp (103%, 59%, and 89%, respectively). The amount of atelectasis decreased more in ALIexp than in ALIp (from 58% to 19% and from 59% to 33%, respectively). RMs augmented type III procollagen messenger RNA expression only in the ALIp group (19%), associated with worsening in alveolar epithelium injury but no capillary endothelium lesion, whereas the ALIexp group showed a minor detachment of the alveolar capillary membrane.
CONCLUSIONS:Given the same transpulmonary pressures, RMs are more effective at opening collapsed alveoli in ALIexp than in ALIp, thus improving lung mechanics and oxygenation with limited damage to alveolar epithelium.</description><subject>Airway Resistance - physiology</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Capillary Permeability - physiology</subject><subject>Collagen Type III - genetics</subject><subject>Disease Models, Animal</subject><subject>Endothelium, Vascular - pathology</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Gene Expression - physiology</subject><subject>Intensive care medicine</subject><subject>Lung Compliance - physiology</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Oxygen - blood</subject><subject>Pneumology</subject><subject>Pulmonary Alveoli - blood supply</subject><subject>Pulmonary Alveoli - pathology</subject><subject>Pulmonary Alveoli - physiopathology</subject><subject>Pulmonary Atelectasis - pathology</subject><subject>Pulmonary Atelectasis - physiopathology</subject><subject>Pulmonary Gas Exchange - physiology</subject><subject>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Respiratory Distress Syndrome, Adult - pathology</subject><subject>Respiratory Distress Syndrome, Adult - physiopathology</subject><subject>Respiratory Mechanics - physiology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>Systemic Inflammatory Response Syndrome - pathology</subject><subject>Systemic Inflammatory Response Syndrome - physiopathology</subject><issn>0090-3493</issn><issn>1530-0293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoun78A5Fe9FadbNI2OcriFyiCH-cyTadaTds1aVz990Z2UfDgaWB43uGZl7F9DsccdHEym90cQwVckOCKFzlQVq-xCc8EpDDVYp1NADSkQmqxxba9fwHgMivEJtviSupc5DBh93dkXGjHjvox6bCn8E4uaftkHmw39Og-E-zrhD5Gh78r-piTa78zaBM0YaTEhv4p5l6C-9xlGw1aT3urucMez88eZpfp9e3F1ez0OjVCyTrVIupkaLIGMIoqEfXqpqqgyrnOoZAm07xCBYi6MZhV2OSy1mZaTSUZVYgddrS8O3fDWyA_ll3rDVkb3xiCLwueC1loFUG5BI0bvHfUlPNoHx8pOZTfZZaxzPJvmTF2sLofqo7q39CqvQgcrgD0Bm3jsDet_-GmIJTKtIycWnKLwY7k_KsNC3LlM6Edn_93-AJsspGZ</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Riva, Douglas R</creator><creator>Oliveira, Mariana B. G</creator><creator>Rzezinski, Andréia F</creator><creator>Rangel, Graziela</creator><creator>Capelozzi, Vera L</creator><creator>Zin, Walter A</creator><creator>Morales, Marcelo M</creator><creator>Pelosi, Paolo</creator><creator>Rocco, Patricia R. M</creator><general>by the Society of Critical Care Medicine and Lippincott Williams & Wilkins</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>200806</creationdate><title>Recruitment maneuver in pulmonary and extrapulmonary experimental acute lung injury</title><author>Riva, Douglas R ; Oliveira, Mariana B. G ; Rzezinski, Andréia F ; Rangel, Graziela ; Capelozzi, Vera L ; Zin, Walter A ; Morales, Marcelo M ; Pelosi, Paolo ; Rocco, Patricia R. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384d-931455ac5f0a09083014dfbb0b6196074c591ba80aa9fca5baf64d9c2b24ec873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Airway Resistance - physiology</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Capillary Permeability - physiology</topic><topic>Collagen Type III - genetics</topic><topic>Disease Models, Animal</topic><topic>Endothelium, Vascular - pathology</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Gene Expression - physiology</topic><topic>Intensive care medicine</topic><topic>Lung Compliance - physiology</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Oxygen - blood</topic><topic>Pneumology</topic><topic>Pulmonary Alveoli - blood supply</topic><topic>Pulmonary Alveoli - pathology</topic><topic>Pulmonary Alveoli - physiopathology</topic><topic>Pulmonary Atelectasis - pathology</topic><topic>Pulmonary Atelectasis - physiopathology</topic><topic>Pulmonary Gas Exchange - physiology</topic><topic>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Respiratory Distress Syndrome, Adult - pathology</topic><topic>Respiratory Distress Syndrome, Adult - physiopathology</topic><topic>Respiratory Mechanics - physiology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>Systemic Inflammatory Response Syndrome - pathology</topic><topic>Systemic Inflammatory Response Syndrome - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Riva, Douglas R</creatorcontrib><creatorcontrib>Oliveira, Mariana B. G</creatorcontrib><creatorcontrib>Rzezinski, Andréia F</creatorcontrib><creatorcontrib>Rangel, Graziela</creatorcontrib><creatorcontrib>Capelozzi, Vera L</creatorcontrib><creatorcontrib>Zin, Walter A</creatorcontrib><creatorcontrib>Morales, Marcelo M</creatorcontrib><creatorcontrib>Pelosi, Paolo</creatorcontrib><creatorcontrib>Rocco, Patricia R. M</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>Critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Riva, Douglas R</au><au>Oliveira, Mariana B. G</au><au>Rzezinski, Andréia F</au><au>Rangel, Graziela</au><au>Capelozzi, Vera L</au><au>Zin, Walter A</au><au>Morales, Marcelo M</au><au>Pelosi, Paolo</au><au>Rocco, Patricia R. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recruitment maneuver in pulmonary and extrapulmonary experimental acute lung injury</atitle><jtitle>Critical care medicine</jtitle><addtitle>Crit Care Med</addtitle><date>2008-06</date><risdate>2008</risdate><volume>36</volume><issue>6</issue><spage>1900</spage><epage>1908</epage><pages>1900-1908</pages><issn>0090-3493</issn><eissn>1530-0293</eissn><coden>CCMDC7</coden><abstract>OBJECTIVE:The aim of this study is to test the hypothesis that recruitment maneuvers (RMs) might act differently in models of pulmonary (p) and extrapulmonary (exp) acute lung injury (ALI) with similar transpulmonary pressure changes.
DESIGN:Prospective, randomized, controlled experimental study.
SETTING:University research laboratory.
SUBJECTS:Wistar rats were randomly divided into four groups. In control groups, sterile saline solution was intratracheally (0.1 mL, Cp) or intraperitoneally (1 mL, Cexp) injected, whereas ALI animals received Escherichia coli lipopolysaccharide intratracheally (100 μg, ALIp) or intraperitoneally (1 mg, ALIexp). After 24 hrs, animals were mechanically ventilated (tidal volume, 6 mL/kg; positive end-expiratory pressure, 5 cm H2O) and three RMs (pressure inflations to 40 cm H2O for 40 secs, 1 min apart) applied.
MEASUREMENTS AND MAIN RESULTS:Pao2, lung resistive and viscoelastic pressures, static elastance, lung histology (light and electron microscopy), and type III procollagen messenger RNA expression in pulmonary tissue were measured before RMs and at the end of 1 hr of mechanical ventilation. Mechanical variables, gas exchange, and the fraction of area of alveolar collapse were similar in both ALI groups. After RMs, lung resistive and viscoelastic pressures and static elastance decreased more in ALIexp (255%, 180%, and 118%, respectively) than in ALIp (103%, 59%, and 89%, respectively). The amount of atelectasis decreased more in ALIexp than in ALIp (from 58% to 19% and from 59% to 33%, respectively). RMs augmented type III procollagen messenger RNA expression only in the ALIp group (19%), associated with worsening in alveolar epithelium injury but no capillary endothelium lesion, whereas the ALIexp group showed a minor detachment of the alveolar capillary membrane.
CONCLUSIONS:Given the same transpulmonary pressures, RMs are more effective at opening collapsed alveoli in ALIexp than in ALIp, thus improving lung mechanics and oxygenation with limited damage to alveolar epithelium.</abstract><cop>Hagerstown, MD</cop><pub>by the Society of Critical Care Medicine and Lippincott Williams & Wilkins</pub><pmid>18496360</pmid><doi>10.1097/CCM.0b013e3181760e5d</doi><tpages>9</tpages></addata></record> |
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subjects | Airway Resistance - physiology Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Capillary Permeability - physiology Collagen Type III - genetics Disease Models, Animal Endothelium, Vascular - pathology Endothelium, Vascular - physiopathology Gene Expression - physiology Intensive care medicine Lung Compliance - physiology Medical sciences Microscopy, Electron Oxygen - blood Pneumology Pulmonary Alveoli - blood supply Pulmonary Alveoli - pathology Pulmonary Alveoli - physiopathology Pulmonary Atelectasis - pathology Pulmonary Atelectasis - physiopathology Pulmonary Gas Exchange - physiology Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases Rats Rats, Wistar Respiratory Distress Syndrome, Adult - pathology Respiratory Distress Syndrome, Adult - physiopathology Respiratory Mechanics - physiology Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics Systemic Inflammatory Response Syndrome - pathology Systemic Inflammatory Response Syndrome - physiopathology |
title | Recruitment maneuver in pulmonary and extrapulmonary experimental acute lung injury |
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