Inspiration regulates the rate and temporal pattern of lung liquid clearance and lung aeration at birth
1 Department of Physiology, 2 School of Physics, 3 Monash Centre for Synchrotron Science, and 4 Department of Biological Engineering, Monash University, Melbourne; 5 The Division of Newborn Services, Royal Women's Hospital, Carlton, Victoria, Australia; and 6 SPring-8, Japan Synchrotron Radiati...
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container_title | Journal of applied physiology (1985) |
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creator | Siew, Melissa L Wallace, Megan J Kitchen, Marcus J Lewis, Robert A Fouras, Andreas te Pas, Arjan B Yagi, Naoto Uesugi, Kentaro Siu, Karen K. W Hooper, Stuart B |
description | 1 Department of Physiology, 2 School of Physics, 3 Monash Centre for Synchrotron Science, and 4 Department of Biological Engineering, Monash University, Melbourne; 5 The Division of Newborn Services, Royal Women's Hospital, Carlton, Victoria, Australia; and 6 SPring-8, Japan Synchrotron Radiation Research Institute, Sayo, Hyogo, Japan
Submitted 24 November 2008
; accepted in final form 31 March 2009
At birth, the initiation of pulmonary gas exchange is dependent on air entry into the lungs, and recent evidence indicates that pressures generated by inspiration may be involved. We have used simultaneous plethysmography and phase-contrast X-ray imaging to investigate the contribution of inspiration and expiratory braking maneuvers (EBMs) to lung aeration and the formation of a functional residual capacity (FRC) after birth. Near-term rabbit pups ( n = 26) were delivered by cesarean section, placed in a water plethysmograph, and imaged during the initiation of spontaneous breathing. Breath-by-breath changes in lung gas volumes were measured using plethysmography and visualized using phase-contrast X-ray imaging. Pups rapidly (1–5 breaths) generate a FRC (16.2 ± 1.2 ml/kg) by inhaling a greater volume than they expire (by 2.9 ± 0.4 ml·kg –1 ·breath –1 over the first 5 breaths). As a result, 94.8 ± 1.4% of lung aeration occurred during inspiration over multiple breaths. The incidence of EBMs was rare early during lung aeration, with most (>80%) occurring after >80% of max FRC was achieved. Although EBMs were associated with an overall increase in FRC, 34.8 ± 5.3% of EBMs were associated with a decrease in FRC. We conclude that lung aeration is predominantly achieved by inspiratory efforts and that EBMs help to maintain FRC following its formation.
fetus; expiratory braking maneuvers
Address for reprint requests and other correspondence: S. B. Hooper, Dept. of Physiology, Monash Univ., Melbourne, Victoria 3800, Australia (e-mail: stuart.hooper{at}med.monash.edu.au ) |
doi_str_mv | 10.1152/japplphysiol.91526.2008 |
format | Article |
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Submitted 24 November 2008
; accepted in final form 31 March 2009
At birth, the initiation of pulmonary gas exchange is dependent on air entry into the lungs, and recent evidence indicates that pressures generated by inspiration may be involved. We have used simultaneous plethysmography and phase-contrast X-ray imaging to investigate the contribution of inspiration and expiratory braking maneuvers (EBMs) to lung aeration and the formation of a functional residual capacity (FRC) after birth. Near-term rabbit pups ( n = 26) were delivered by cesarean section, placed in a water plethysmograph, and imaged during the initiation of spontaneous breathing. Breath-by-breath changes in lung gas volumes were measured using plethysmography and visualized using phase-contrast X-ray imaging. Pups rapidly (1–5 breaths) generate a FRC (16.2 ± 1.2 ml/kg) by inhaling a greater volume than they expire (by 2.9 ± 0.4 ml·kg –1 ·breath –1 over the first 5 breaths). As a result, 94.8 ± 1.4% of lung aeration occurred during inspiration over multiple breaths. The incidence of EBMs was rare early during lung aeration, with most (>80%) occurring after >80% of max FRC was achieved. Although EBMs were associated with an overall increase in FRC, 34.8 ± 5.3% of EBMs were associated with a decrease in FRC. We conclude that lung aeration is predominantly achieved by inspiratory efforts and that EBMs help to maintain FRC following its formation.
fetus; expiratory braking maneuvers
Address for reprint requests and other correspondence: S. B. Hooper, Dept. of Physiology, Monash Univ., Melbourne, Victoria 3800, Australia (e-mail: stuart.hooper{at}med.monash.edu.au )</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.91526.2008</identifier><identifier>PMID: 19342434</identifier><identifier>CODEN: JAPHEV</identifier><language>eng</language><publisher>Bethesda, MD: Am Physiological Soc</publisher><subject>Animals ; Animals, Newborn ; Biological and medical sciences ; Births ; Extravascular Lung Water - metabolism ; Female ; Fundamental and applied biological sciences. Psychology ; Inhalation - physiology ; Lung - diagnostic imaging ; Lung - physiology ; Lungs ; Medical imaging ; Parturition - physiology ; Phase Transition ; Physiology ; Pregnancy ; Pulmonary Gas Exchange - physiology ; Rabbits ; Radiography ; Respiratory system ; X-rays</subject><ispartof>Journal of applied physiology (1985), 2009-06, Vol.106 (6), p.1888-1895</ispartof><rights>2009 INIST-CNRS</rights><rights>Copyright American Physiological Society Jun 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-abf51d182983c2adbf453f9cfbc82fcfddf0bbb81272be938648a74b684da5ac3</citedby><cites>FETCH-LOGICAL-c402t-abf51d182983c2adbf453f9cfbc82fcfddf0bbb81272be938648a74b684da5ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21540359$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19342434$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Siew, Melissa L</creatorcontrib><creatorcontrib>Wallace, Megan J</creatorcontrib><creatorcontrib>Kitchen, Marcus J</creatorcontrib><creatorcontrib>Lewis, Robert A</creatorcontrib><creatorcontrib>Fouras, Andreas</creatorcontrib><creatorcontrib>te Pas, Arjan B</creatorcontrib><creatorcontrib>Yagi, Naoto</creatorcontrib><creatorcontrib>Uesugi, Kentaro</creatorcontrib><creatorcontrib>Siu, Karen K. W</creatorcontrib><creatorcontrib>Hooper, Stuart B</creatorcontrib><title>Inspiration regulates the rate and temporal pattern of lung liquid clearance and lung aeration at birth</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>1 Department of Physiology, 2 School of Physics, 3 Monash Centre for Synchrotron Science, and 4 Department of Biological Engineering, Monash University, Melbourne; 5 The Division of Newborn Services, Royal Women's Hospital, Carlton, Victoria, Australia; and 6 SPring-8, Japan Synchrotron Radiation Research Institute, Sayo, Hyogo, Japan
Submitted 24 November 2008
; accepted in final form 31 March 2009
At birth, the initiation of pulmonary gas exchange is dependent on air entry into the lungs, and recent evidence indicates that pressures generated by inspiration may be involved. We have used simultaneous plethysmography and phase-contrast X-ray imaging to investigate the contribution of inspiration and expiratory braking maneuvers (EBMs) to lung aeration and the formation of a functional residual capacity (FRC) after birth. Near-term rabbit pups ( n = 26) were delivered by cesarean section, placed in a water plethysmograph, and imaged during the initiation of spontaneous breathing. Breath-by-breath changes in lung gas volumes were measured using plethysmography and visualized using phase-contrast X-ray imaging. Pups rapidly (1–5 breaths) generate a FRC (16.2 ± 1.2 ml/kg) by inhaling a greater volume than they expire (by 2.9 ± 0.4 ml·kg –1 ·breath –1 over the first 5 breaths). As a result, 94.8 ± 1.4% of lung aeration occurred during inspiration over multiple breaths. The incidence of EBMs was rare early during lung aeration, with most (>80%) occurring after >80% of max FRC was achieved. Although EBMs were associated with an overall increase in FRC, 34.8 ± 5.3% of EBMs were associated with a decrease in FRC. We conclude that lung aeration is predominantly achieved by inspiratory efforts and that EBMs help to maintain FRC following its formation.
fetus; expiratory braking maneuvers
Address for reprint requests and other correspondence: S. B. Hooper, Dept. of Physiology, Monash Univ., Melbourne, Victoria 3800, Australia (e-mail: stuart.hooper{at}med.monash.edu.au )</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Births</subject><subject>Extravascular Lung Water - metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Inhalation - physiology</subject><subject>Lung - diagnostic imaging</subject><subject>Lung - physiology</subject><subject>Lungs</subject><subject>Medical imaging</subject><subject>Parturition - physiology</subject><subject>Phase Transition</subject><subject>Physiology</subject><subject>Pregnancy</subject><subject>Pulmonary Gas Exchange - physiology</subject><subject>Rabbits</subject><subject>Radiography</subject><subject>Respiratory system</subject><subject>X-rays</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd-L1DAQx4Mo3t7pv6BB8MCHrkmatOmjHP44OPBFn8MkTbpZsm0vSZH9701vi4rzkmHyme8M80XoLSV7SgX7eIR5DvPhnPwU9l2pNHtGiHyGdiVnFW0IfY52shWkaoVsr9B1SkdCKOeCvkRXtKs54zXfoeF-TLOPkP004miHJUC2CeeDxaVoMYw9zvY0TxECniFnG0c8ORyWccDBPy6-xyZYiDCaC_30A3aThIy1j_nwCr1wEJJ9vb036OeXzz_uvlUP37_e3316qAwnLFegnaA9layTtWHQa8dF7TrjtJHMGdf3jmitJWUt07arZcMltFw3kvcgwNQ36PaiO8fpcbEpq5NPxoYAo52WpJqWSd5JUcB3_4HHaYlj2U2xNaQgTYHaC2TilFK0Ts3RnyCeFSVqNUL9a4R6MkKtRpTON5v8ok-2_9u3Xb4A7zcAkoHg1gP69IdjVHBSi65wHy7cwQ-HXz5atU2bhvM6vWzSqEZRKWX9G8l9paU</recordid><startdate>20090601</startdate><enddate>20090601</enddate><creator>Siew, Melissa L</creator><creator>Wallace, Megan J</creator><creator>Kitchen, Marcus J</creator><creator>Lewis, Robert A</creator><creator>Fouras, Andreas</creator><creator>te Pas, Arjan B</creator><creator>Yagi, Naoto</creator><creator>Uesugi, Kentaro</creator><creator>Siu, Karen K. 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Psychology</topic><topic>Inhalation - physiology</topic><topic>Lung - diagnostic imaging</topic><topic>Lung - physiology</topic><topic>Lungs</topic><topic>Medical imaging</topic><topic>Parturition - physiology</topic><topic>Phase Transition</topic><topic>Physiology</topic><topic>Pregnancy</topic><topic>Pulmonary Gas Exchange - physiology</topic><topic>Rabbits</topic><topic>Radiography</topic><topic>Respiratory system</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Siew, Melissa L</creatorcontrib><creatorcontrib>Wallace, Megan J</creatorcontrib><creatorcontrib>Kitchen, Marcus J</creatorcontrib><creatorcontrib>Lewis, Robert A</creatorcontrib><creatorcontrib>Fouras, Andreas</creatorcontrib><creatorcontrib>te Pas, Arjan B</creatorcontrib><creatorcontrib>Yagi, Naoto</creatorcontrib><creatorcontrib>Uesugi, Kentaro</creatorcontrib><creatorcontrib>Siu, Karen K. 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W</au><au>Hooper, Stuart B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inspiration regulates the rate and temporal pattern of lung liquid clearance and lung aeration at birth</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2009-06-01</date><risdate>2009</risdate><volume>106</volume><issue>6</issue><spage>1888</spage><epage>1895</epage><pages>1888-1895</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><coden>JAPHEV</coden><abstract>1 Department of Physiology, 2 School of Physics, 3 Monash Centre for Synchrotron Science, and 4 Department of Biological Engineering, Monash University, Melbourne; 5 The Division of Newborn Services, Royal Women's Hospital, Carlton, Victoria, Australia; and 6 SPring-8, Japan Synchrotron Radiation Research Institute, Sayo, Hyogo, Japan
Submitted 24 November 2008
; accepted in final form 31 March 2009
At birth, the initiation of pulmonary gas exchange is dependent on air entry into the lungs, and recent evidence indicates that pressures generated by inspiration may be involved. We have used simultaneous plethysmography and phase-contrast X-ray imaging to investigate the contribution of inspiration and expiratory braking maneuvers (EBMs) to lung aeration and the formation of a functional residual capacity (FRC) after birth. Near-term rabbit pups ( n = 26) were delivered by cesarean section, placed in a water plethysmograph, and imaged during the initiation of spontaneous breathing. Breath-by-breath changes in lung gas volumes were measured using plethysmography and visualized using phase-contrast X-ray imaging. Pups rapidly (1–5 breaths) generate a FRC (16.2 ± 1.2 ml/kg) by inhaling a greater volume than they expire (by 2.9 ± 0.4 ml·kg –1 ·breath –1 over the first 5 breaths). As a result, 94.8 ± 1.4% of lung aeration occurred during inspiration over multiple breaths. The incidence of EBMs was rare early during lung aeration, with most (>80%) occurring after >80% of max FRC was achieved. Although EBMs were associated with an overall increase in FRC, 34.8 ± 5.3% of EBMs were associated with a decrease in FRC. We conclude that lung aeration is predominantly achieved by inspiratory efforts and that EBMs help to maintain FRC following its formation.
fetus; expiratory braking maneuvers
Address for reprint requests and other correspondence: S. B. Hooper, Dept. of Physiology, Monash Univ., Melbourne, Victoria 3800, Australia (e-mail: stuart.hooper{at}med.monash.edu.au )</abstract><cop>Bethesda, MD</cop><pub>Am Physiological Soc</pub><pmid>19342434</pmid><doi>10.1152/japplphysiol.91526.2008</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; American Physiological Society Paid; Free E-Journal (出版社公開部分のみ); Alma/SFX Local Collection |
subjects | Animals Animals, Newborn Biological and medical sciences Births Extravascular Lung Water - metabolism Female Fundamental and applied biological sciences. Psychology Inhalation - physiology Lung - diagnostic imaging Lung - physiology Lungs Medical imaging Parturition - physiology Phase Transition Physiology Pregnancy Pulmonary Gas Exchange - physiology Rabbits Radiography Respiratory system X-rays |
title | Inspiration regulates the rate and temporal pattern of lung liquid clearance and lung aeration at birth |
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