IMR Press / CEOG / Volume 37 / Issue 1 / pii/1630629621298-1634661302

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 47 Issue 1 (2020). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Original Research
Effects of selective and non-selective cyclooxygenase (COX) inhibitors on postoperative adhesion formation in a rat uterine horn model
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1 Department of Obstetrics and Gynecology, Celal Bayar University School of Medicine, Manisa
2 Department of Obstetrics and Gynecology, Jinepark Private Women Health Clinic, Sanliurfa
3 Department of Obstetrics and Gynecology, Ercis State Hospital, Van
4 Department of Obstetrics and Gynecology, Cumhuriyet University School of Medicine, Sivas (Turkey)
Clin. Exp. Obstet. Gynecol. 2010, 37(1), 49–52;
Published: 10 March 2010
Abstract

Objective: To investigate the effects of cyclooxygenase (COX) inhibitors including celecoxib, indomethacin, and nimesulide on postoperative adhesion formation. Material and Methods: Forty-eight female Wistar-Albino rats were randomly divided into four groups: control (saline solution), celecoxib, indomethacin, and nimesulide groups. The uterine horns of rats were traumatized with unipolar electrocautery. Drugs of each group and saline in the control group were insillated on travmatized areas of horns as intraperitoneally. After three weeks, the extent and severity of adhesions with a standardized scoring system were evaluated. Results: The extent and severity of postoperative adhesions were significantly reduced in nimesulide group compared with the control group. The extent but not severity of adhesions in rats given indomethacin was significantly reduced. Celecoxib showed no significant reduction in the extent and severity of adhesions. Conclusion: Nimesulide is more effective than the other COX inhibitors in the prevention of postoperative adhesions in rats.
Keywords
Adhesion
Cyclooxygenase
Nimesulide
Celecoxib
Indomethacin
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