Prone position prevents regional alveolar hyperinflation and mechanical stress and strain in mild experimental acute lung injury

Abstract Prone position may delay the development of ventilator-induced lung injury (VILI), but the mechanisms require better elucidation. In experimental mild acute lung injury (ALI), arterial oxygen partial pressure ( P a O 2 ), lung mechanics and histology, inflammatory markers [interleukin (IL)-...

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Veröffentlicht in:Respiratory physiology & neurobiology 2009-06, Vol.167 (2), p.181-188
Hauptverfasser: Santana, Maria Cristina E, Garcia, Cristiane S.N.B, Xisto, Débora G, Nagato, Lilian K.S, Lassance, Roberta M, Prota, Luiz Felipe M, Ornellas, Felipe M, Capelozzi, Vera L, Morales, Marcelo M, Zin, Walter A, Pelosi, Paolo, Rocco, Patricia R.M
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container_end_page 188
container_issue 2
container_start_page 181
container_title Respiratory physiology & neurobiology
container_volume 167
creator Santana, Maria Cristina E
Garcia, Cristiane S.N.B
Xisto, Débora G
Nagato, Lilian K.S
Lassance, Roberta M
Prota, Luiz Felipe M
Ornellas, Felipe M
Capelozzi, Vera L
Morales, Marcelo M
Zin, Walter A
Pelosi, Paolo
Rocco, Patricia R.M
description Abstract Prone position may delay the development of ventilator-induced lung injury (VILI), but the mechanisms require better elucidation. In experimental mild acute lung injury (ALI), arterial oxygen partial pressure ( P a O 2 ), lung mechanics and histology, inflammatory markers [interleukin (IL)-6 and IL-1β], and type III procollagen (PCIII) mRNA expressions were analysed in supine and prone position. Wistar rats were randomly divided into two groups. In controls, saline was intraperitoneally injected while ALI was induced by paraquat. After 24-h, the animals were mechanically ventilated for 1-h in supine or prone positions. In ALI, prone position led to a better blood flow/tissue ratio both in ventral and dorsal regions and was associated with a more homogeneous distribution of alveolar aeration/tissue ratio reducing lung static elastance and viscoelastic pressure, and increasing end-expiratory lung volume and P a O 2 . PCIII expression was higher in the ventral than dorsal region in supine position, with no regional changes in inflammatory markers. In conclusion, prone position may protect the lungs against VILI, thus reducing pulmonary stress and strain.
doi_str_mv 10.1016/j.resp.2009.04.006
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In experimental mild acute lung injury (ALI), arterial oxygen partial pressure ( P a O 2 ), lung mechanics and histology, inflammatory markers [interleukin (IL)-6 and IL-1β], and type III procollagen (PCIII) mRNA expressions were analysed in supine and prone position. Wistar rats were randomly divided into two groups. In controls, saline was intraperitoneally injected while ALI was induced by paraquat. After 24-h, the animals were mechanically ventilated for 1-h in supine or prone positions. In ALI, prone position led to a better blood flow/tissue ratio both in ventral and dorsal regions and was associated with a more homogeneous distribution of alveolar aeration/tissue ratio reducing lung static elastance and viscoelastic pressure, and increasing end-expiratory lung volume and P a O 2 . PCIII expression was higher in the ventral than dorsal region in supine position, with no regional changes in inflammatory markers. 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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Acute Lung Injury - metabolism
Acute Lung Injury - pathology
Acute Lung Injury - physiopathology
Animals
Biological and medical sciences
Female
Fundamental and applied biological sciences. Psychology
Gas-exchange
Inflammation Mediators - metabolism
Interleukin-1beta - biosynthesis
Interleukin-6 - biosynthesis
Lung histopathology
Lung mechanics
Medical Education
Oxygen
Partial Pressure
Procollagen - biosynthesis
Prone Position - physiology
Pulmonary Alveoli - physiopathology
Pulmonary/Respiratory
Rats
Rats, Wistar
Respiratory Mechanics - physiology
RNA, Messenger - analysis
Tissue stress and strain
Ventilator-induced lung injury
Vertebrates: respiratory system
Vital Capacity - physiology
title Prone position prevents regional alveolar hyperinflation and mechanical stress and strain in mild experimental acute lung injury
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