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环氧化酶抑制剂能否作为治疗卵巢过度刺激综合征的一种选择?

Can a cyclooxygenase inhibitor be an option for treatment of ovarian hyperstimulation syndrome?

作者信息

Çilgin Hasan

机构信息

Medicine Faculty, Obstetrics and Gynecology Department, Kafkas University, Kars, Turkey,

出版信息

Drug Des Devel Ther. 2019 Apr 5;13:1099-1105. doi: 10.2147/DDDT.S188583. eCollection 2019.

Abstract

PURPOSE

This study aimed to investigate the role of a cyclooxygenase inhibitor in ovarian hyperstimulation syndrome (OHSS) treatment and compare it with cabergoline.

MATERIALS AND METHODS

A total of 32 immature female Wistar albino rats were randomly divided into four groups, with each group consisting of eight rats. The first group received only saline for 6 consecutive days, and the remaining 24 rats were given 10 IU of recombinant follicle stimulating hormone subcutaneously on 5 consecutive days. On day 6, 30 IU of human chorionic gonadotropin was administered for OHSS induction. After the development of OHSS, while the second group had no further intervention, the third and fourth groups were given cabergoline and celecoxib daily for 6 days, respectively. Besides weight and hematocrit values, vascular endothelial growth factor (VEGF), IL-2, and endothelin-1 (ET-1) levels were evaluated.

RESULTS

Initially, no significant differences were observed between the groups with respect to the evaluated parameters. Although there were no differences between the weight and hema-tocrit values at the end of treatment (=0.158, =0.674), the difference between group 1 and the other groups was statistically significant after OHSS was established (=0.001, =0.004). Comparison of the groups in terms of VEGF, ET-1, and IL-2 levels revealed that the difference between group 1 and the other groups was significant after OHSS was formed (=0.012, =0.018, =0.015). After treatment, however, a significant difference was observed only between group 2 and the other groups (=0.001, =0.002, =0.038).

CONCLUSION

According to these results, celecoxib significantly decreased VEGF, IL-2, and ET-1 levels as much as cabergoline and could reduce the extent of OHSS development.

摘要

目的

本研究旨在探讨环氧化酶抑制剂在卵巢过度刺激综合征(OHSS)治疗中的作用,并将其与卡麦角林进行比较。

材料与方法

总共32只未成熟雌性Wistar白化大鼠被随机分为四组,每组8只。第一组连续6天仅接受生理盐水,其余24只大鼠连续5天皮下注射10国际单位重组促卵泡激素。在第6天,给予30国际单位人绒毛膜促性腺激素以诱导OHSS。OHSS形成后,第二组不进行进一步干预,第三组和第四组分别每天给予卡麦角林和塞来昔布,持续6天。除体重和血细胞比容值外,还评估了血管内皮生长因子(VEGF)、白细胞介素-2(IL-2)和内皮素-1(ET-1)水平。

结果

最初,各组在评估参数方面未观察到显著差异。虽然治疗结束时体重和血细胞比容值之间没有差异(P = 0.158,P = 0.674),但在OHSS形成后,第一组与其他组之间的差异具有统计学意义(P = 0.001,P = 0.004)。在VEGF、ET-1和IL-2水平方面对各组进行比较发现,在OHSS形成后,第一组与其他组之间的差异显著(P = 0.012,P = 0.018,P = 0.015)。然而,治疗后,仅在第二组与其他组之间观察到显著差异(P = 0.001,P = 0.002,P = 0.038)。

结论

根据这些结果,塞来昔布与卡麦角林一样能显著降低VEGF、IL-2和ET-1水平,并可减轻OHSS的发展程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c0c/6454993/66443be2dadb/dddt-13-1099Fig1.jpg

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