Hypervolemia induces and potentiates lung damage after recruitment maneuver in a model of sepsis-induced acute lung injury
Recruitment maneuvers (RMs) seem to be more effective in extrapulmonary acute lung injury (ALI), caused mainly by sepsis, than in pulmonary ALI. Nevertheless, the maintenance of adequate volemic status is particularly challenging in sepsis. Since the interaction between volemic status and RMs is not...
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creator | Silva, Pedro L Cruz, Fernanda F Fujisaki, Livia C Oliveira, Gisele P Samary, Cynthia S Ornellas, Debora S Maron-Gutierrez, Tatiana Rocha, Nazareth N Goldenberg, Regina Garcia, Cristiane S N B Morales, Marcelo M Capelozzi, Vera L Gama de Abreu, Marcelo Pelosi, Paolo Rocco, Patricia R M |
description | Recruitment maneuvers (RMs) seem to be more effective in extrapulmonary acute lung injury (ALI), caused mainly by sepsis, than in pulmonary ALI. Nevertheless, the maintenance of adequate volemic status is particularly challenging in sepsis. Since the interaction between volemic status and RMs is not well established, we investigated the effects of RMs on lung and distal organs in the presence of hypovolemia, normovolemia, and hypervolemia in a model of extrapulmonary lung injury induced by sepsis.
ALI was induced by cecal ligation and puncture surgery in 66 Wistar rats. After 48 h, animals were anesthetized, mechanically ventilated and randomly assigned to 3 volemic status (n = 22/group): 1) hypovolemia induced by blood drainage at mean arterial pressure (MAP) approximately 70 mmHg; 2) normovolemia (MAP approximately 100 mmHg), and 3) hypervolemia with colloid administration to achieve a MAP approximately 130 mmHg. In each group, animals were further randomized to be recruited (CPAP = 40 cm H2O for 40 s) or not (NR) (n = 11/group), followed by 1 h of protective mechanical ventilation. Echocardiography, arterial blood gases, static lung elastance (Est,L), histology (light and electron microscopy), lung wet-to-dry (W/D) ratio, interleukin (IL)-6, IL-1beta, caspase-3, type III procollagen (PCIII), intercellular adhesion molecule-1 (ICAM-1), and vascular cell adhesion molecule-1 (VCAM-1) mRNA expressions in lung tissue, as well as lung and distal organ epithelial cell apoptosis were analyzed.
We observed that: 1) hypervolemia increased lung W/D ratio with impairment of oxygenation and Est,L, and was associated with alveolar and endothelial cell damage and increased IL-6, VCAM-1, and ICAM-1 mRNA expressions; and 2) RM reduced alveolar collapse independent of volemic status. In hypervolemic animals, RM improved oxygenation above the levels observed with the use of positive-end expiratory pressure (PEEP), but increased lung injury and led to higher inflammatory and fibrogenetic responses.
Volemic status should be taken into account during RMs, since in this sepsis-induced ALI model hypervolemia promoted and potentiated lung injury compared to hypo- and normovolemia. |
doi_str_mv | 10.1186/cc9063 |
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ALI was induced by cecal ligation and puncture surgery in 66 Wistar rats. After 48 h, animals were anesthetized, mechanically ventilated and randomly assigned to 3 volemic status (n = 22/group): 1) hypovolemia induced by blood drainage at mean arterial pressure (MAP) approximately 70 mmHg; 2) normovolemia (MAP approximately 100 mmHg), and 3) hypervolemia with colloid administration to achieve a MAP approximately 130 mmHg. In each group, animals were further randomized to be recruited (CPAP = 40 cm H2O for 40 s) or not (NR) (n = 11/group), followed by 1 h of protective mechanical ventilation. Echocardiography, arterial blood gases, static lung elastance (Est,L), histology (light and electron microscopy), lung wet-to-dry (W/D) ratio, interleukin (IL)-6, IL-1beta, caspase-3, type III procollagen (PCIII), intercellular adhesion molecule-1 (ICAM-1), and vascular cell adhesion molecule-1 (VCAM-1) mRNA expressions in lung tissue, as well as lung and distal organ epithelial cell apoptosis were analyzed.
We observed that: 1) hypervolemia increased lung W/D ratio with impairment of oxygenation and Est,L, and was associated with alveolar and endothelial cell damage and increased IL-6, VCAM-1, and ICAM-1 mRNA expressions; and 2) RM reduced alveolar collapse independent of volemic status. In hypervolemic animals, RM improved oxygenation above the levels observed with the use of positive-end expiratory pressure (PEEP), but increased lung injury and led to higher inflammatory and fibrogenetic responses.
Volemic status should be taken into account during RMs, since in this sepsis-induced ALI model hypervolemia promoted and potentiated lung injury compared to hypo- and normovolemia.</description><identifier>ISSN: 1364-8535</identifier><identifier>EISSN: 1466-609X</identifier><identifier>EISSN: 1364-8535</identifier><identifier>DOI: 10.1186/cc9063</identifier><identifier>PMID: 20546573</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acute Lung Injury - etiology ; Acute Lung Injury - physiopathology ; Acute Lung Injury - therapy ; Acute respiratory distress syndrome ; Animals ; Apoptosis - physiology ; Blood circulation disorders ; Blood Volume ; Brazil ; Complications and side effects ; Lung diseases ; Microscopy, Electron ; Models, Animal ; Patient outcomes ; Positive-Pressure Respiration ; Pulmonary Alveoli - physiopathology ; Random Allocation ; Rats ; Rats, Wistar ; Respiration, Artificial ; Risk factors ; Sepsis - complications ; Sepsis - physiopathology ; Treatment Outcome</subject><ispartof>Critical care (London, England), 2010-01, Vol.14 (3), p.R114-R114, Article R114</ispartof><rights>COPYRIGHT 2010 BioMed Central Ltd.</rights><rights>Copyright National Library of Medicine - MEDLINE Abstracts 2010</rights><rights>Copyright ©2010 Silva et al.; licensee BioMed Central Ltd. 2010 Silva et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b541t-8b747a0c689bcbae4eeee74ec2542fe948377cd249691634bd749f76ab2bc3683</citedby><cites>FETCH-LOGICAL-b541t-8b747a0c689bcbae4eeee74ec2542fe948377cd249691634bd749f76ab2bc3683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911760/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911760/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20546573$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silva, Pedro L</creatorcontrib><creatorcontrib>Cruz, Fernanda F</creatorcontrib><creatorcontrib>Fujisaki, Livia C</creatorcontrib><creatorcontrib>Oliveira, Gisele P</creatorcontrib><creatorcontrib>Samary, Cynthia S</creatorcontrib><creatorcontrib>Ornellas, Debora S</creatorcontrib><creatorcontrib>Maron-Gutierrez, Tatiana</creatorcontrib><creatorcontrib>Rocha, Nazareth N</creatorcontrib><creatorcontrib>Goldenberg, Regina</creatorcontrib><creatorcontrib>Garcia, Cristiane S N B</creatorcontrib><creatorcontrib>Morales, Marcelo M</creatorcontrib><creatorcontrib>Capelozzi, Vera L</creatorcontrib><creatorcontrib>Gama de Abreu, Marcelo</creatorcontrib><creatorcontrib>Pelosi, Paolo</creatorcontrib><creatorcontrib>Rocco, Patricia R M</creatorcontrib><title>Hypervolemia induces and potentiates lung damage after recruitment maneuver in a model of sepsis-induced acute lung injury</title><title>Critical care (London, England)</title><addtitle>Crit Care</addtitle><description>Recruitment maneuvers (RMs) seem to be more effective in extrapulmonary acute lung injury (ALI), caused mainly by sepsis, than in pulmonary ALI. Nevertheless, the maintenance of adequate volemic status is particularly challenging in sepsis. Since the interaction between volemic status and RMs is not well established, we investigated the effects of RMs on lung and distal organs in the presence of hypovolemia, normovolemia, and hypervolemia in a model of extrapulmonary lung injury induced by sepsis.
ALI was induced by cecal ligation and puncture surgery in 66 Wistar rats. After 48 h, animals were anesthetized, mechanically ventilated and randomly assigned to 3 volemic status (n = 22/group): 1) hypovolemia induced by blood drainage at mean arterial pressure (MAP) approximately 70 mmHg; 2) normovolemia (MAP approximately 100 mmHg), and 3) hypervolemia with colloid administration to achieve a MAP approximately 130 mmHg. In each group, animals were further randomized to be recruited (CPAP = 40 cm H2O for 40 s) or not (NR) (n = 11/group), followed by 1 h of protective mechanical ventilation. Echocardiography, arterial blood gases, static lung elastance (Est,L), histology (light and electron microscopy), lung wet-to-dry (W/D) ratio, interleukin (IL)-6, IL-1beta, caspase-3, type III procollagen (PCIII), intercellular adhesion molecule-1 (ICAM-1), and vascular cell adhesion molecule-1 (VCAM-1) mRNA expressions in lung tissue, as well as lung and distal organ epithelial cell apoptosis were analyzed.
We observed that: 1) hypervolemia increased lung W/D ratio with impairment of oxygenation and Est,L, and was associated with alveolar and endothelial cell damage and increased IL-6, VCAM-1, and ICAM-1 mRNA expressions; and 2) RM reduced alveolar collapse independent of volemic status. In hypervolemic animals, RM improved oxygenation above the levels observed with the use of positive-end expiratory pressure (PEEP), but increased lung injury and led to higher inflammatory and fibrogenetic responses.
Volemic status should be taken into account during RMs, since in this sepsis-induced ALI model hypervolemia promoted and potentiated lung injury compared to hypo- and normovolemia.</description><subject>Acute Lung Injury - etiology</subject><subject>Acute Lung Injury - physiopathology</subject><subject>Acute Lung Injury - therapy</subject><subject>Acute respiratory distress syndrome</subject><subject>Animals</subject><subject>Apoptosis - physiology</subject><subject>Blood circulation disorders</subject><subject>Blood Volume</subject><subject>Brazil</subject><subject>Complications and side effects</subject><subject>Lung diseases</subject><subject>Microscopy, Electron</subject><subject>Models, Animal</subject><subject>Patient outcomes</subject><subject>Positive-Pressure Respiration</subject><subject>Pulmonary Alveoli - physiopathology</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Respiration, Artificial</subject><subject>Risk factors</subject><subject>Sepsis - complications</subject><subject>Sepsis - physiopathology</subject><subject>Treatment Outcome</subject><issn>1364-8535</issn><issn>1466-609X</issn><issn>1364-8535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkt9vFCEQxzdGY2vVP8EQTezTVlhYfryYNI22Jk180cQ3wrKzJ5ddWGG55Pzr5bK1ekYjPADDZ74MM1NVzwm-IETyN9YqzOmD6pQwzmuO1ZeHZU85q2VL25PqSUpbjImQnD6uThrcMt4Kelp9v9nPEHdhhMkZ5HyfLSRkfI_msIBfnFnKecx-g3ozmQ0gMywQUQQbs1umgqDJeMi7YnQeGTSFHkYUBpRgTi7Vq2aPjM0LrErOb3PcP60eDWZM8OxuPas-v3_36eqmvv14_eHq8rbuWkaWWnaCCYMtl6qznQEGZQgGtmlZM4Bikgph-4YprginrOsFU4Pgpms6S7mkZ9XbVXfO3QS9LSFHM-o5usnEvQ7G6eMb777qTdjpRhEiOC4CahXoXPiHwPGNDZNeC1J8z-8ej-FbhrToySUL41hyFnLSomVt-SYT_yeZVLJUVBXy5R_kNuToSw61oIwWqjkE_WqFNmYE7fwQSmj2IKkvG4oFobI9UBd_ocrsSz_Y4GFwxX7k8Hp1sDGkFGG4TwPB-tCJvz7-4ves32M_W4_-AMK023A</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Silva, Pedro L</creator><creator>Cruz, Fernanda F</creator><creator>Fujisaki, Livia C</creator><creator>Oliveira, Gisele P</creator><creator>Samary, Cynthia S</creator><creator>Ornellas, Debora S</creator><creator>Maron-Gutierrez, Tatiana</creator><creator>Rocha, Nazareth N</creator><creator>Goldenberg, Regina</creator><creator>Garcia, Cristiane S N B</creator><creator>Morales, Marcelo M</creator><creator>Capelozzi, Vera L</creator><creator>Gama de Abreu, Marcelo</creator><creator>Pelosi, Paolo</creator><creator>Rocco, Patricia R M</creator><general>BioMed Central Ltd</general><general>National Library of Medicine - MEDLINE Abstracts</general><general>BioMed Central</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>K9.</scope><scope>7X8</scope><scope>7QL</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20100101</creationdate><title>Hypervolemia induces and potentiates lung damage after recruitment maneuver in a model of sepsis-induced acute lung injury</title><author>Silva, Pedro L ; Cruz, Fernanda F ; Fujisaki, Livia C ; Oliveira, Gisele P ; Samary, Cynthia S ; Ornellas, Debora S ; Maron-Gutierrez, Tatiana ; Rocha, Nazareth N ; Goldenberg, Regina ; Garcia, Cristiane S N B ; Morales, Marcelo M ; Capelozzi, Vera L ; Gama de Abreu, Marcelo ; Pelosi, Paolo ; Rocco, Patricia R M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b541t-8b747a0c689bcbae4eeee74ec2542fe948377cd249691634bd749f76ab2bc3683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acute Lung Injury - etiology</topic><topic>Acute Lung Injury - physiopathology</topic><topic>Acute Lung Injury - therapy</topic><topic>Acute respiratory distress syndrome</topic><topic>Animals</topic><topic>Apoptosis - physiology</topic><topic>Blood circulation disorders</topic><topic>Blood Volume</topic><topic>Brazil</topic><topic>Complications and side effects</topic><topic>Lung diseases</topic><topic>Microscopy, Electron</topic><topic>Models, Animal</topic><topic>Patient outcomes</topic><topic>Positive-Pressure Respiration</topic><topic>Pulmonary Alveoli - physiopathology</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Respiration, Artificial</topic><topic>Risk factors</topic><topic>Sepsis - complications</topic><topic>Sepsis - physiopathology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silva, Pedro L</creatorcontrib><creatorcontrib>Cruz, Fernanda F</creatorcontrib><creatorcontrib>Fujisaki, Livia C</creatorcontrib><creatorcontrib>Oliveira, Gisele P</creatorcontrib><creatorcontrib>Samary, Cynthia S</creatorcontrib><creatorcontrib>Ornellas, Debora S</creatorcontrib><creatorcontrib>Maron-Gutierrez, Tatiana</creatorcontrib><creatorcontrib>Rocha, Nazareth N</creatorcontrib><creatorcontrib>Goldenberg, Regina</creatorcontrib><creatorcontrib>Garcia, Cristiane S N B</creatorcontrib><creatorcontrib>Morales, Marcelo M</creatorcontrib><creatorcontrib>Capelozzi, Vera L</creatorcontrib><creatorcontrib>Gama de Abreu, Marcelo</creatorcontrib><creatorcontrib>Pelosi, Paolo</creatorcontrib><creatorcontrib>Rocco, Patricia R M</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 Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Critical care (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silva, Pedro L</au><au>Cruz, Fernanda F</au><au>Fujisaki, Livia C</au><au>Oliveira, Gisele P</au><au>Samary, Cynthia S</au><au>Ornellas, Debora S</au><au>Maron-Gutierrez, Tatiana</au><au>Rocha, Nazareth N</au><au>Goldenberg, Regina</au><au>Garcia, Cristiane S N B</au><au>Morales, Marcelo M</au><au>Capelozzi, Vera L</au><au>Gama de Abreu, Marcelo</au><au>Pelosi, Paolo</au><au>Rocco, Patricia R M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypervolemia induces and potentiates lung damage after recruitment maneuver in a model of sepsis-induced acute lung injury</atitle><jtitle>Critical care (London, England)</jtitle><addtitle>Crit Care</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>14</volume><issue>3</issue><spage>R114</spage><epage>R114</epage><pages>R114-R114</pages><artnum>R114</artnum><issn>1364-8535</issn><eissn>1466-609X</eissn><eissn>1364-8535</eissn><abstract>Recruitment maneuvers (RMs) seem to be more effective in extrapulmonary acute lung injury (ALI), caused mainly by sepsis, than in pulmonary ALI. Nevertheless, the maintenance of adequate volemic status is particularly challenging in sepsis. Since the interaction between volemic status and RMs is not well established, we investigated the effects of RMs on lung and distal organs in the presence of hypovolemia, normovolemia, and hypervolemia in a model of extrapulmonary lung injury induced by sepsis.
ALI was induced by cecal ligation and puncture surgery in 66 Wistar rats. After 48 h, animals were anesthetized, mechanically ventilated and randomly assigned to 3 volemic status (n = 22/group): 1) hypovolemia induced by blood drainage at mean arterial pressure (MAP) approximately 70 mmHg; 2) normovolemia (MAP approximately 100 mmHg), and 3) hypervolemia with colloid administration to achieve a MAP approximately 130 mmHg. In each group, animals were further randomized to be recruited (CPAP = 40 cm H2O for 40 s) or not (NR) (n = 11/group), followed by 1 h of protective mechanical ventilation. Echocardiography, arterial blood gases, static lung elastance (Est,L), histology (light and electron microscopy), lung wet-to-dry (W/D) ratio, interleukin (IL)-6, IL-1beta, caspase-3, type III procollagen (PCIII), intercellular adhesion molecule-1 (ICAM-1), and vascular cell adhesion molecule-1 (VCAM-1) mRNA expressions in lung tissue, as well as lung and distal organ epithelial cell apoptosis were analyzed.
We observed that: 1) hypervolemia increased lung W/D ratio with impairment of oxygenation and Est,L, and was associated with alveolar and endothelial cell damage and increased IL-6, VCAM-1, and ICAM-1 mRNA expressions; and 2) RM reduced alveolar collapse independent of volemic status. In hypervolemic animals, RM improved oxygenation above the levels observed with the use of positive-end expiratory pressure (PEEP), but increased lung injury and led to higher inflammatory and fibrogenetic responses.
Volemic status should be taken into account during RMs, since in this sepsis-induced ALI model hypervolemia promoted and potentiated lung injury compared to hypo- and normovolemia.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>20546573</pmid><doi>10.1186/cc9063</doi><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection; SpringerLink Journals - AutoHoldings; Springer Nature OA Free Journals |
subjects | Acute Lung Injury - etiology Acute Lung Injury - physiopathology Acute Lung Injury - therapy Acute respiratory distress syndrome Animals Apoptosis - physiology Blood circulation disorders Blood Volume Brazil Complications and side effects Lung diseases Microscopy, Electron Models, Animal Patient outcomes Positive-Pressure Respiration Pulmonary Alveoli - physiopathology Random Allocation Rats Rats, Wistar Respiration, Artificial Risk factors Sepsis - complications Sepsis - physiopathology Treatment Outcome |
title | Hypervolemia induces and potentiates lung damage after recruitment maneuver in a model of sepsis-induced acute lung injury |
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