Journal of Applied Physiology Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


J Appl Physiol (November 2, 2006). doi:10.1152/japplphysiol.01139.2005
This Article
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
102/2/762    most recent
01139.2005v1
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
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 Google Scholar
Google Scholar
Right arrow Articles by Tsang, J. Y.
Right arrow Articles by Hlastala, M. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tsang, J. Y.
Right arrow Articles by Hlastala, M. P.
Submitted on September 12, 2005
Accepted on October 10, 2006

Endothelin Receptor Blockade Does not Improve Hypoxemia Following Acute Pulmonary Thromboembolism

John YC Tsang1*, Wayne JE Lamm2, Blazej Neradilek3, Nayak L Polissar3, and Michael P. Hlastala4

1 James Hogg iCAPTURE Research Laboratory, University of British Columbia, Vancouver, Canada
2 Medicine, University of Washington, Seattle, Washington, United States
3 Mountain-Whisper-Light Statistical Consulting, Seattle, Washington, United States
4 Physiology & Biophysics, University of Washington, Seattle, Washington, United States; Medicine, University of Washington, Seattle, Washington, United States

* To whom correspondence should be addressed. E-mail: jtsang{at}interchange.ubc.ca.

We studied the roles of endothelins in determining ventilation (VA) and perfusion (Q) mismatch in a porcine model of acute pulmonary thromboembolism (APTE), using a non-specific endothelin antagonist, Tezosentan. Nine anaesthetized piglets (~23 Kg) received autologous clots (~20 gm) via a central venous catheter at time = 0 mins. The distribution of VA and Q at 5 different time points (-30, -5, 30, 60, 120 mins) was mapped by fluorescent microspheres of 10 different colors. 5 piglets (Group 1) received Tezosentan (courtesy Actelion Ltd) starting at time = 40 mins for 2 hours and 4 piglets (Group 2) received only saline and served as control. Our results showed that in all of the animals at 30 mins following APTE but prior to Tezosentan, the mean VA/Q was increased as did VA/Q heterogeneity (Log SD VA/Q), which represented a widening of its main peak. Afterwards Tezosentan attenuated the pulmonary hypertension in Group 1 but also produced moderate systemic hypotension. However, it did not improve PaO2 or VA/Q mismatch. We concluded that endothelins had minimal impact on gas exchange following APTE and confirmed our earlier observation that the main mechanism for hypoxemia in APTE was due to the mechanical redistribution of pulmonary regional blood flow away from the embolized vessels, resulting in the creation of many divergent low and high VA/Q regions.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 1948 by the American Physiological Society.