Cyclooxygenase-2 selective inhibitor prevents implantation of eutopic endometrium to ectopic sites in rats

被引:101
作者
Matsuzaki, S
Canis, M
Darcha, C
Dallel, R
Okamura, K
Mage, G
机构
[1] CHU Clermont Ferrand, Dept Gynecol, Polyclin Hotel Dieu, F-63058 Clermont Ferrand 1, France
[2] Tohoku Univ, Sch Med, Sendai, Miyagi 980, Japan
关键词
cyclooxygenase-2; Cox-2; cyclooxygenase-2 selective inhibitor; endometriosis; rat model;
D O I
10.1016/j.fertnstert.2004.07.946
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Objective: To evaluate Cox-2 inhibition on surgically induced endometriosis in rats. Design: Prospective, randomized study Setting: Academic facility. Animal(s): Seventy adult female Sprague-Dawley rats. Intervention(s): Uterine fragments were implanted into abdominal peritoneum with suture (site A), and/or into the pelvic cavity without suture (site B). Oral gavage of Cox-2 inhibitor (5 mg/kg/day, twice/day) was started 4 weeks postimplantation (protocol-1), after implantation (protocol-2), or beforehand (protocol-3). Controls received vehicle. Immunohistochemistry evaluated Cox-2 expression after treatment. Main Outcome Measurement(s): Presence and size of ectopic implants after treatment. Result(s): Protocol-1: After 4 weeks' treatment, size of ectopic implants (site A) was significantly reduced compared with pretreatment size. After 8 weeks' treatment, no ectopic implants were detected in 2 (40%, site A) and 3 (60%, site B) rats. Protocol-2: After 2 weeks' treatment, no ectopic implants were detected in 3 (50%, site A) and 2 (33%, site B) rats. After 4 weeks' treatment, no ectopic implants were detected in 3 (50%, site A) and 3 (50%, site B) rats. Protocol-3: After 2 or 4 weeks' vehicle-only treatment, ectopic implants were in all rats (site B). Conclusion(s): Cox-2 selective inhibition was effective in a rat model of endometriosis, particularly in prevention of ectopic implants. (C) 2004 by American Society for Reproductive Medicine.)
引用
收藏
页码:1609 / 1615
页数:7
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