Priddy A R, Killick S R, Elstein M, Morris J, Sullivan M, Patel L, Elder M
Department of Obstetrics and Gynaecology, University Hospital of South Manchester, United Kingdom.
J Clin Endocrinol Metab. 1990 Jul;71(1):235-42. doi: 10.1210/jcem-71-1-235.
This study evaluates the eicosanoid concentration in luteinized unruptured follicles (LUFs) on the ovaries of patients who had been treated with inhibitors of prostaglandin synthetase. Indomethacin, bromfenac, or azapropazone (or a placebo) was administered orally to 41 women during the periovulatory period. Follicular development was monitored by serial ultrasound examinations, and the onset of ovulation was regulated by an injection of hCG. Follicular fluid was aspirated during sterilization by minilaparotomy, which was performed just before the expected time of ovulation. Prostaglandin E2 and PGF2 alpha levels in the fluid were significantly reduced by indomethacin and bromfenac compared to those after placebo treatment. Bromfenac also reduced the follicular fluid leukotriene B4 level. Therefore, the development of luteinized unruptured follicles after treatment with nonsteroidal antiinflammatory drugs appears to be associated with a significant decrease in the synthesis of ovarian eicosanoids.
本研究评估了接受前列腺素合成酶抑制剂治疗的患者卵巢上黄素化未破裂卵泡(LUFs)中类花生酸的浓度。在排卵期,对41名女性口服吲哚美辛、溴芬酸或阿扎丙宗(或安慰剂)。通过连续超声检查监测卵泡发育,并通过注射人绒毛膜促性腺激素(hCG)来调节排卵时间。在预期排卵时间前,通过迷你剖腹术进行绝育时抽取卵泡液。与安慰剂治疗后相比,吲哚美辛和溴芬酸可显著降低卵泡液中前列腺素E2和前列腺素F2α的水平。溴芬酸还降低了卵泡液中白三烯B4的水平。因此,非甾体抗炎药治疗后黄素化未破裂卵泡的形成似乎与卵巢类花生酸合成的显著减少有关。