ATS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
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 Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Masayuki Haniuda
Carolyn M. Dresler
Seiki Hasegawa
Joel D. Cooper
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Haniuda, M.
Right arrow Articles by Cooper, J. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Haniuda, M.
Right arrow Articles by Cooper, J. D.

Ann Thorac Surg 1994;57:708-714
© 1994 The Society of Thoracic Surgeons


Articles

Changes in vascular permeability with ischemic time, temperature, and inspired oxygen fraction in isolated rabbit lungs

Masayuki Haniuda, MD, Carolyn M. Dresler, MD, Seiki Hasegawa, MD, G.Alexander Patterson, MD, Joel D. Cooper, MD*

Division of Cardiothoracic Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri USA

Accepted for publication June 25, 1993.

* Address reprint requests to Dr Cooper, Division of Cardiothoracic Surgery, Washington University, Suite 3108, Queeny Tower, One Barnes Hospital Plaza, St. Louis, MO 63110.

The capillary filtration coefficient (Kf) is one of the most accurate measures of change in pulmonary vascular permeability and has been used in various models of acute lung injury. To evaluate the isolated effects of ischemia on Kf, we have developed an ex vivo rabbit lung model in which the influences of reperfusion are eliminated. The current study was designed to validate this model by determining the effect of cold flushing with low-potassium-dextran solution containing 1% glucose (LPDG), ischemic time, temperature, and inspired oxygen fraction on Kf. On completion of the ischemic period, the ventilated lungs, with the heart still attached, were suspended from a strain-gauge force transducer. After the lungs were flushed with 50 mL hetastarch solution (6% hetastarch solution with physiologic saline solution), the left atrial drainage cannula was occluded and the pulmonary artery pressure was incrementally increased by elevation of the reservoir. The Kf was calculated as the slope of the line relating the weight gain rate and pulmonary capillary pressure. Our study demonstrated the following: (1) Kf was not altered by flushing the lungs with LPDG at either 1 °C or 10 °C; (2) preservation at 37 °C, even for only 2 hours, demonstrated severe deterioration in Kf; (3) although hypothermia during ischemia suppressed the deterioration of Kf, there were no significant differences in Kf between 1 °C and 10 °C when ischemic time was less than 24 hours; (4) when preservation lasted less than 8 hours, change in Kf was not influenced by the differences in inspired oxygen fraction during the ischemic period; (5) during 24-hour preservation, Kf increased less when the lungs were inflated with room air than when they were inflated with either 100% oxygen or 100% nitrogen. These results indicate that injury occurs primarily during ischemia and increases with ischemic lime even in lungs flushed with LPDG and kept at 1 °C or 10 °C. Inflation with 100% oxygen may cause injury of the pulmonary vascular endothelium during 24-hour preservation, although oxygen supply from airway is essential. This isolated, ex vivo rabbit model examining pulmonary vascular permeability provides a sensitive and reliable means for evaluation of ischemic injury of the preserved lung.




This article has been cited by other articles:


Home page
Ann. Thorac. Surg.Home page
S. Y. Lopukhin, D. R. Onsager, R. L. Conhaim, J. H. Southard, and R. B. Love
University of Wisconsin solution with butanedione monoxime and calcium improves rat lung preservation
Ann. Thorac. Surg., January 1, 1999; 67(1): 203 - 207.
[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
J. Appl. Physiol.Home page
D. R. Jones, R. M. Becker, S. C. Hoffmann, J. J. Lemasters, and T. M. Egan
When does the lung die? Kfc, cell viability, and adenine nucleotide changes in the circulation-arrested rat lung
J Appl Physiol, July 1, 1997; 83(1): 247 - 252.
[Abstract] [Full Text] [PDF]


Home page
J. Thorac. Cardiovasc. Surg.Home page
M. Haniuda, S. Hasegawa, T. Shiraishi, C. M. Dresler, J. D. Cooper, and G. A. Patterson
EFFECTS OF INFLATION VOLUME DURING LUNG PRESERVATION ON PULMONARY CAPILLARY PERMEABILITY
J. Thorac. Cardiovasc. Surg., July 1, 1996; 112(1): 85 - 93.
[Abstract] [Full Text]


Home page
Ann. Thorac. Surg.Home page
M. Haniuda, C. M. Dresler, T. Mizuta, J. D. Cooper, and G. A. Patterson
Free radical--mediated vascular injury in lungs preserved at moderate hypothermia
Ann. Thorac. Surg., November 1, 1995; 60(5): 1376 - 1381.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS
Copyright © 1994 by The Society of Thoracic Surgeons.