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


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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):
Minxin Wei
Pekka Kuukasjärvi
Jari Laurikka
Matti Tarkka
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 Wei, M.
Right arrow Articles by Tarkka, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wei, M.
Right arrow Articles by Tarkka, M.
Related Collections
Right arrow Myocardial protection

Ann Thorac Surg 2004;78:492-497
© 2004 The Society of Thoracic Surgeons


Original article: cardiovascular

Bradykinin preconditioning in coronary artery bypass grafting

Minxin Wei, MD, PhDa,c, Xin Wang, MDa, Pekka Kuukasjärvi, MD, PhDa, Jari Laurikka, MD, PhDa, Timo Rinne, MD, PhDb, Eva-Liisa Honkonen, MD, PhDb, Matti Tarkka, MD, PhDa*

a Division of Cardiothoracic Surgery, Tampere University Hospital, Tampere, Finland
b Department of Anesthesia and Intensive Care, Tampere University Hospital, Tampere, Finland
c Division of Cardiac Surgery, Tianjin Chest Hospital, Tianjin, People's Republic of China

Accepted for publication November 25, 2003.

* Address reprint requests to Dr Tarkka, Division of Cardiothoracic Surgery, Tampere University Hospital, PO Box 2000, Fin-33521 Tampere, Finland
e-mail: matti.tarkka{at}pshp.fi

BACKGROUND: Experimental studies have shown that activation of bradykinin B2 receptor is one of the most important triggers of ischemic preconditioning. However, the effect of exogenous administration of bradykinin in cardiac surgery is not yet known. The present prospective randomized study was designed to investigate the effect of bradykinin pretreatment in patients undergoing elective coronary artery bypass surgery.

METHODS: Forty-one patients with multiple-vessel coronary artery disease and stable angina, admitted for the first time for elective coronary artery bypass surgery, were randomized into control or bradykinin (BK) groups. Patients in the BK group received bradykinin infusion for 7 minutes (total dose 25 µg) before the initiation of cardiopulmonary bypass. Perioperative cardiac specific troponin I (cTnI) and creatine kinase cardiac isoenzyme (CKMB) release and hemodynamics were recorded.

RESULTS: Bradykinin infusion caused acute decrease of blood pressure in most of the cases and the mean minimum mean blood pressure during bradykinin infusion was 72.7% of the original mean blood pressure (MBP) level (74.7 ± 7.9 vs 54.4 ± 12.1 mm Hg, p < 0.01). There were no differences in baseline levels of cTnI and CKMB between the groups. The postoperative cTnI levels were lower than 10 ng/mL in most patients in both groups (18 in the BK group and 15 in the control group). There was no difference in cTnI between the groups. However, patients who received bradykinin released significantly less CKMB than did the controls postoperatively (6 hours, BK, 22.1 ± 9.5 vs control, 23.6 ± 12.7 U/L; 12 hours, BK, 19.4 ± 12.4 vs control, 28.7 ± 23.8 U/L; 24 hours, BK, 21.5 ± 14.7 vs control, 35.5 ± 28.9 U/L; 48 hours, BK, 14.4 ± 7.5 vs control, 23.5 ± 13.6 U/L; analysis of variance [ANOVA] for repeated measurement, p = 0.036). Maximum CKMB was also lower in the BK group (22.4 ± 14.4 vs 37.7 ± 27.5 U/L, p = 0.044). There was no significant difference between the groups in any of the hemodynamic variables.

CONCLUSIONS: Exogenous bradykinin infusion showed weak cardioprotective effect in the low-risk patients undergoing coronary artery bypass surgery but the dose used in the study caused acute decrease of systemic blood pressure.




This article has been cited by other articles:


Home page
CirculationHome page
J. Feng, C. Bianchi, J. L. Sandmeyer, and F. W. Sellke
Bradykinin Preconditioning Improves the Profile of Cell Survival Proteins and Limits Apoptosis After Cardioplegic Arrest
Circulation, August 30, 2005; 112(9_suppl): I-190 - I-195.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
J. Feng, C. Bianchi, J. Li, and F. W. Sellke
Bradykinin Preconditioning Preserves Coronary Microvascular Reactivity During Cardioplegia-Reperfusion
Ann. Thorac. Surg., March 1, 2005; 79(3): 911 - 916.
[Abstract] [Full Text] [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 © 2004 by The Society of Thoracic Surgeons.