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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Veröffentlicht in:Journal of applied physiology (1985) 2009-06, Vol.106 (6), p.1888-1895
Hauptverfasser: 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
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container_end_page 1895
container_issue 6
container_start_page 1888
container_title Journal of applied physiology (1985)
container_volume 106
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
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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 (&gt;80%) occurring after &gt;80% of max FRC was achieved. 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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. 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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 (&gt;80%) occurring after &gt;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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ispartof Journal of applied physiology (1985), 2009-06, Vol.106 (6), p.1888-1895
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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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