Correlation Engine 2.0
Clear Search sequence regions


Pentoxifylline (Ptx) decreases necessity of cell energy and inflammatory reactions via inhibition of 5'-nucleotidase (5'-NT). The aim of this study is to investigate whether the addition of Ptx into the cardioplegic solutions avoids myocardial inflammatory reactions and ischemia/reperfusion (I/R) injury during extracorpereal circulation. Between December 1999 and February 2002, we operated 75 patients with the diagnoses of atrial septal defect (ASD), ventricular septal defect (VSD), valve disease, and coronary disease. The average age of patients was 42.4 and male-female ratio was 1: 1.5. The patients were divided into two groups, which were the study group (n = 40) and the control group (n = 35). We used cold blood cardioplegia mixed with St. Thomas' Hospital II cardioplegic solution for both of the groups. Ptx was added into the cardioplegic solution (500 mg/L) in the study group. Interleukin-6 (IL-6), interleukin-8 (IL-8), and tumor necrotisis factor-alpha (TNF-alpha) levels in coronary sinus blood samples during cross-clamp time (X-clamp) and after releasing of it and tissue TNF-alpha in the right atrial appendix biopsy material that was taken after X-clamp were studied to compare the both groups. After releasing X-clamp, results of blood TNF-alpha, IL-6, and IL-8 of both groups were statistically significant (p < 0.005). At the pathological examination, we also observed that the amount of tissue TNF-alpha in the control group (66 +/- 17.1) was much higher than the study group (16.6 +/- 5.9, p <0.005). These results show that Ptx may be added into cardioplegic solution to avoid the myocardial inflammation and I/R injury during open heart surgery.

Citation

Hasim Ustunsoy, M Cumhur Sivrikoz, Mehmet Tarakcioglu, Kemal Bakir, Emin Guldur, M Adnan Celkan. The effects of pentoxifylline on the myocardial inflammation and ischemia-reperfusion injury during cardiopulmonary bypass. Journal of cardiac surgery. 2006 Jan-Feb;21(1):57-61

Expand section icon Mesh Tags

Expand section icon Substances


PMID: 16426349

View Full Text