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


     


This Article
Right arrow Full Text
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):
Yuji Shiraishi
Jeong Ryul Lee
Hillel Laks
Paul F. Waters
Arie Blitz
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 Shiraishi, Y.
Right arrow Articles by Chang, P. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shiraishi, Y.
Right arrow Articles by Chang, P. A.
Related Collections
Right arrowRelated Articles

Ann Thorac Surg 1996;62:1580-1586
© 1996 The Society of Thoracic Surgeons


Original Articles: General Thoracic

L-Arginine Administration During Reperfusion Improves Pulmonary Function

Yuji Shiraishi, MD, Jeong Ryul Lee, MD, Hillel Laks, MD, Paul F. Waters, MD, Avedis Meneshian, BS, Arie Blitz, MD, Keith Johnson, BS, Lydia Lam, BS, Paul A. Chang, BS

Division of Cardiothoracic Surgery, University of California, Los Angeles, Medical Center, Los Angeles, California

Background. Nitric oxide is crucial to the maintenance of vascular homeostasis. Because nitric oxide levels decline upon lung reperfusion, infusion of L-arginine, a nitric oxide precursor, during reperfusion might prove effective at ameliorating reperfusion injury.

Methods. Neonatal piglet heart-lung blocks were preserved with Euro-Collins solution for 12 hours, rewarmed at room temperature for 1 hour, and reperfused for 10 minutes with either whole blood (n = 5), whole blood containing L-arginine (10 mmol/L; n = 6), or leukocyte-depleted blood (n = 6) on an isolated, blood-perfused, working heart-lung circuit. After the initial 10 minutes, all blocks received whole blood for 4 hours. Control blocks were continuously perfused on the circuit without intervening ischemia (n = 6).

Results. The partial pressure of oxygen in the whole blood group (113.8 ± 33.1 mm Hg) was significantly less than in controls (417.3 ± 6.2 mm Hg; p < 0.01). Lung compliance was significantly less in the whole blood group (0.8 ± 0.2 mL/cm H2O) than in controls (2.9 ± 0.4 mL/cm H2O; p < 0.01). The L-arginine and leukocyte-depleted blood groups showed no significant difference from controls.

Conclusions. L-Arginine infusion during reperfusion improves pulmonary function, making it a simple alternative to leukocyte depletion.


Related Articles

Discussion
Ann. Thorac. Surg. 1996 62: 1586. [Extract] [Full Text]

Invited Commentary
David J. Pinsky
Ann. Thorac. Surg. 1996 62: 1586-1587. [Extract] [Full Text]



This article has been cited by other articles:


Home page
Ann. Thorac. Surg.Home page
Y. Yang, Z. Su, J. Cai, S. Wang, J. Liu, Z. Xu, and W. Ding
Continuous pulmonary infusion of L-arginine during deep hypothermia and circulatory arrest improves pulmonary surfactant integrity in piglets.
Ann. Thorac. Surg., August 1, 2008; 86(2): 429 - 435.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
M. de Perrot, M. Liu, T. K. Waddell, and S. Keshavjee
Ischemia-Reperfusion-induced Lung Injury
Am. J. Respir. Crit. Care Med., February 15, 2003; 167(4): 490 - 511.
[Abstract] [Full Text] [PDF]


Home page
Eur. J. Cardiothorac. Surg.Home page
S. Hillinger, P. Sandera, G. L. Carboni, U. Stammberger, M. Zalunardo, G. Schoedon, and R. A. Schmid
Survival and graft function in a large animal lung transplant model after 30 h preservation and substitution of the nitric oxide pathway
Eur. J. Cardiothorac. Surg., September 1, 2001; 20(3): 508 - 513.
[Abstract] [Full Text] [PDF]


Home page
J. Thorac. Cardiovasc. Surg.Home page
R. A. Schmid, S. Hillinger, R. Walter, A. Zollinger, U. Stammberger, R. Speich, A. Schaffner, W. Weder, and G. Schoedon
THE NITRIC OXIDE SYNTHASE COFACTOR TETRAHYDROBIOPTERIN REDUCES ALLOGRAFT ISCHEMIA-REPERFUSION INJURY AFTER LUNG TRANSPLANTATION
J. Thorac. Cardiovasc. Surg., October 1, 1999; 118(4): 726 - 732.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
S. Hillinger, R. A. Schmid, P. Sandera, U. Stammberger, D. Schneiter, G. Schoedon, and W. Weder
8-Br-cGMP is superior to prostaglandin e1 for lung preservation
Ann. Thorac. Surg., October 1, 1999; 68(4): 1138 - 1142.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
O. D. SCHNEUWLY, M. LICKER, C. M. PASTOR, A. SCHWEIZER, D. O. SLOSMAN, Y. KAPANCI, L. P. NICOD, J. ROBERT, A. SPILIOPOULOS, and D. R. MOREL
Beneficial Effects of Leukocyte-depleted Blood and Low-potassium Dextran Solutions on Microvascular Permeability in Preserved Porcine Lung
Am. J. Respir. Crit. Care Med., August 1, 1999; 160(2): 689 - 697.
[Abstract] [Full Text]




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 © 1996 by The Society of Thoracic Surgeons.