Effect of diclofenac on cyclooxygenase-2 levels and early breaking strength of experimental colonic anastomoses and skin incisions

Eur Surg Res. 2011;46(1):26-31. doi: 10.1159/000321706. Epub 2010 Dec 7.

Abstract

Background: Recently, there has been a focus on the effect of the nonsteroidal anti-inflammatory drugs on the anastomotic leakage rate after colorectal surgery.

Methods: An experimental, randomized, placebo-controlled prospective study on 32 male Wistar rats was carried out. We examined the effect of diclofenac 4 mg/kg/day on the cyclooxygenase-2 (COX-2) enzyme in the anastomotic tissue and on the breaking strength of anastomotic and incisional wounds. The operation was performed with colonic resection and hand-sewn anastomosis. After 3 days, the rats were sacrificed and the breaking strength and the COX-2 content of the anastomosis were measured.

Results: There was a significantly reduced level of COX-2 in the rats treated with diclofenac (p = 0.001); no significant differences in any of the breaking strength measurements and no significant correlation between COX-2 levels and breaking strength of the anastomotic or incisional wounds could be found (p = 0.073 and p = 0.727).

Conclusion: This study for the first time showed that a diclofenac dose of 4 mg/kg/24 h was sufficient to reduce the level of COX-2 enzymes in the anastomotic tissue in rats. This inhibition of the inflammatory response did not lead to reduced breaking strength of either anastomotic or incisional wounds. Whether there is a detrimental effect of COX inhibition on colorectal anastomoses in the clinical setting remains controversial.

MeSH terms

  • Anastomosis, Surgical
  • Anastomotic Leak / chemically induced*
  • Anastomotic Leak / enzymology
  • Animals
  • Biomechanical Phenomena
  • Colectomy
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase Inhibitors / adverse effects*
  • Dermatologic Surgical Procedures
  • Diclofenac / adverse effects*
  • Male
  • Prospective Studies
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Wound Healing / drug effects*

Substances

  • Cyclooxygenase Inhibitors
  • Diclofenac
  • Cyclooxygenase 2
  • Ptgs2 protein, rat