Journal of Applied Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 73: 2112-2119, 1992;
8750-7587/92 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hamvas, A.
Right arrow Articles by Schuster, D. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hamvas, A.
Right arrow Articles by Schuster, D. P.

Journal of Applied Physiology, Vol 73, Issue 5 2112-2119, Copyright © 1992 by American Physiological Society


ARTICLES

Modifying pulmonary ischemia-reperfusion injury by altering ventilatory strategies during ischemia

A. Hamvas, C. K. Park, R. Palazzo, M. Liptay, J. Cooper and D. P. Schuster
Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110.

We used an intact in vivo canine model of pulmonary ischemia-reperfusion (IR) injury to evaluate the differential effects of alveolar hypoxia and ventilation during 2 h of unilateral warm lung ischemia. Serial measurements of regional pulmonary blood flow, extravascular density (EVD), and transcapillary protein flux were made after reperfusion with the quantitative imaging technique of positron emission tomography. Twenty-seven animals were divided into five experimental groups: VENT O2 (n = 5) in which the left lung was ventilated with 40% O2 during ischemia, STATIC O2 (n = 4) in which the left lung was statically inflated with 40% O2 during ischemia, VENT N2 (n = 5) in which the left lung was ventilated with 100% N2 during ischemia, VENT N2/CO2 (n = 5) in which the left lung was ventilated with 95% N2-5% CO2 during ischemia, and STATIC N2 (n = 8) in which the left lung was statically inflated with 100% N2 during ischemia. These groups were compared with a control group (CONT, = 3) that was studied previously. Protein flux was significantly increased in the previous ischemic lung only for the STATIC N2 group [median 175 x 10(-4) min-1 (range 53-1,217) for the STATIC N2 group vs. 50 x 10(-4) min-1 (range 40-56) for the CONT group] 0.25 h after reperfusion and did not change over 3 h. EVD also increased but not significantly. Protein flux and EVD in the other groups were not different from CONT.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
G. Matute-Bello, C. W. Frevert, and T. R. Martin
Animal models of acute lung injury
Am J Physiol Lung Cell Mol Physiol, September 1, 2008; 295(3): L379 - L399.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
S. V. Baudouin
Lung injury after thoracotomy
Br. J. Anaesth., July 1, 2003; 91(1): 132 - 142.
[Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
H. SCHUTTE, K. MAYER, H. BURGER, M. WITZENRATH, T. GESSLER, W. SEEGER, and F. GRIMMINGER
Endogenous Nitric Oxide Synthesis and Vascular Leakage in Ischemic-Reperfused Rabbit Lungs
Am. J. Respir. Crit. Care Med., August 1, 2001; 164(3): 412 - 418.
[Abstract] [Full Text] [PDF]


Home page
Eur Respir JHome page
H. Schutte, A. Lockinger, W. Seeger, and F. Grimminger
Aerosolized PGE1, PGI2 and nitroprusside protect against vascular leakage in lung ischaemia-reperfusion
Eur. Respir. J., July 1, 2001; 18(1): 15 - 22.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
H. Schutte, M. Witzenrath, K. Mayer, N. Weissmann, A. Schell, S. Rosseau, W. Seeger, and F. Grimminger
The PDE inhibitor zaprinast enhances NO-mediated protection against vascular leakage in reperfused lungs
Am J Physiol Lung Cell Mol Physiol, September 1, 2000; 279(3): L496 - L502.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
H. B. Srinivasan, S. M. Vogel, D. Vidyasagar, and A. B. Malik
Protective effect of lung inflation in reperfusion-induced lung microvascular injury
Am J Physiol Heart Circ Physiol, March 1, 2000; 278(3): H951 - H957.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
G. HERMLE, H. SCHÜTTE, D. WALMRATH, K. GEIGER, W. SEEGER, and F. GRIMMINGER
Ventilation-Perfusion Mismatch after Lung Ischemia-Reperfusion . Protective Effect of Nitric Oxide
Am. J. Respir. Crit. Care Med., October 1, 1999; 160(4): 1179 - 1187.
[Abstract] [Full Text]


Home page
J. Appl. Physiol.Home page
D. B. Pearse, E. M. Wagner, and S. Permutt
Effect of ventilation on vascular permeability and cyclic nucleotide concentrations in ischemic sheep lungs
J Appl Physiol, January 1, 1999; 86(1): 123 - 132.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
T. Sakuma, K. Takahashi, N. Ohya, O. Kajikawa, T. R. Martin, K. H. Albertine, and M. A. Matthay
Ischemia-reperfusion lung injury in rabbits: mechanisms of injury and protection
Am J Physiol Lung Cell Mol Physiol, January 1, 1999; 276(1): L137 - L145.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
H. SCHÜTTE, G. HERMLE, W. SEEGER, and F. GRIMMINGER
Vascular Distension and Continued Ventilation Are Protective in Lung Ischemia/Reperfusion
Am. J. Respir. Crit. Care Med., January 1, 1997; 157(1): 171 - 177.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online