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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Veröffentlicht in:Critical care medicine 2008-06, Vol.36 (6), p.1900-1908
Hauptverfasser: 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
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container_end_page 1908
container_issue 6
container_start_page 1900
container_title Critical care medicine
container_volume 36
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
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G ; Rzezinski, Andréia F ; Rangel, Graziela ; Capelozzi, Vera L ; Zin, Walter A ; Morales, Marcelo M ; Pelosi, Paolo ; Rocco, Patricia R. M</creator><creatorcontrib>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</creatorcontrib><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><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 &amp; 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 &amp; 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&amp;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. 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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 &amp; 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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