Thorac Cardiovasc Surg 2006; 54(8): 506-511
DOI: 10.1055/s-2006-924471
Basic Science

© Georg Thieme Verlag KG Stuttgart · New York

Heparin-Protamine does not Aggravate Local LPS-Provoked Leukocytic Inflammation in Vivo

R. Schramm1 , 2 , R. M. Nickels2 , Y. Harder2 , F. Langer1 , M. D. Menger2 , H.-J. Schäfers1
  • 1Department of Thoracic and Cardiovascular Surgery, University of Saarland, Homburg/Saar, Germany
  • 2Institute for Clinical and Experimental Surgery, University of Saarland, Homburg/Saar, Germany
Further Information

Publication History

Received March 20, 2006

Publication Date:
06 December 2006 (online)

Abstract

Objective: Secondary complications involving inflammation limit postoperative results in cardiac surgery. Because heparin-protamine can elicit inflammatory reactions, this study evaluates in vivo whether treatment with heparin-protamine aggravates local endotoxin-induced injury. Methods: Mice received intravenous injections of either heparin-protamine, protamine alone or PBS for controls, before local air pouch challenge with LPS. Leukocytes recruited within the air pouches were collected and analyzed by flow cytometry. Results: LPS provoked a local leukocytic infiltration in a dose- and time-dependent manner with significantly elevated numbers of 1.75 ± 0.29 × 106 cells after four hours compared to non-LPS-stimulated controls (0.55 ± 0.08 × 106 cells). Recruited cells comprised of 74 ± 4 % PMNLs and 26 ± 4 % MNLs. The largest fraction of MNLs was positive for the T cell-specific marker CD90.2 (59 ± 6 %). B cells were only rarely observed (4 ± 1 %). In non-LPS-challenged air pouches, heparin-protamine provoked a leukocytic infiltration, which was comparable to that observed after LPS (1.51 ± 0.22 × 106 cells). However, neither heparin-protamine nor protamine alone aggravated the LPS-mediated leukocyte recruitment (2.25 ± 0.25 × 106 and 1.77 ± 0.23 × 106 cells). Neither treatment influenced the distribution of leukocyte subpopulations compared to PBS-treated controls. Furthermore, surface expression of CD11a and CD11b on blood leukocytes did not differ between the groups, indicating that protamine does not increase the activation of circulating leukocytes during LPS-induced local inflammation. Conclusions: Our data indicate that heparin-protamine, although pro-inflammatory in nature, does not aggravate local inflammation provoked by LPS. Thus, enhanced inflammation during the perioperative course of cardiac surgery patients seems not to be attributable to the intraoperative use of heparin-protamine.

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MD, PhD René Schramm

Department of Thoracic and Cardiovascular Surgery
University of Saarland

Kirrberger Straße

66421 Homburg/Saar

Germany

Phone: + 49 6 84 11 63 20 00

Fax: + 49 6 84 11 63 20 05

Email: reneschramm@hotmail.com

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