Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

CiteULike is a free service for managing and discovering scholarly references - click here to get started.

Sign In to gain access to subscriptions and/or personal tools.
Perfusion
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
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Loubser, P. G
Right arrow Articles by Buffone, G. J
Right arrow Search for Related Content
PubMed
Right arrow Articles by Loubser, P. G
Right arrow Articles by Buffone, G. J
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

In vitro generation of C3a anaphylatoxin by an extracorporeal circuit

Paul G Loubser

Texas Heart Institute, Houston

Gregory J Buffone

Texas Children's Hospital and Baylor College of Medicine, Houston

The generation of C3a anaphylatoxin was studied during the equilibration of fresh whole blood in an extracorporeal circuit with oxygenator before institution of cardiopulmonary bypass. Twenty-seven units of whole blood were each recirculated through an extracorporeal circuit for periods up to 17 minutes Following an equilibration period of 7 ± 3.5 min, the C3a concentration increased from 563.1 ± 48.4 to 802.1 ± 73.7 ng/ml, corrected for haematocrit (p < 0.01). The increase in C3a was, however, not related to duration of equilibration time. In vivo studies by others reported higher peak levels of C3a and a correlation with duration of cardiopulmonary bypass. Our data confirm that the extracorporeal circuit is an important site of complement activation, but suggest that during cardiopulmonary bypass, other sites or mechanisms may also generate C3a.

Perfusion, Vol. 2, No. 3, 219-222 (1987)
DOI: 10.1177/026765918700200311


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?