The effect of orally and vaginally administered misoprostol on inflammatory mediators and cervical ripening during early pregnancy

被引:18
作者
Aronsson, A
Ulfgren, AK
Ståbi, B
Stavreus-Evers, A
Gemzell-Danielsson, K [1 ]
机构
[1] Karolinska Inst, Div Obstet & Gynecol, Dept Woman & Child Hlth, S-17176 Stockholm, Sweden
[2] Karolinska Inst, Div Obstet & Gynecol, Dept Clin Sci, S-17176 Stockholm, Sweden
关键词
cervical ripening; matrix metalloproteinases; misoprostol; MMP; TIMP;
D O I
10.1016/j.contraception.2005.02.012
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: The objective of the present study was to investigate the effect of vaginally and orally administered misoprostol on the local cervical inflammatory response. Methods: Healthy women with a normal intrauterine pregnancy between 8 and 12 weeks of gestation presenting for an elective termination of pregnancy by vacuum aspiration were recruited into a cohort study with a control and a treatment group. In the treatment group, the women were randomized to misoprostol, 400 mu g, given either orally or vaginally 3 h before surgery. Immunohistochemistry staining of CD45, CD68, MMP 8, MMP 9, TIMP 1 and TIMP 2 were assessed in cervical biopsies obtained directly prior to mechanical cervical dilatation and vacuum aspiration. Results: In the treatment group, there was a greater amount of CD45-positive cells in the subepithelium region of the cervix compared to the control group. The staining of CD68 was similar in both groups. The immunostaining of MMP 8 and MMP 9 was greater in the treatment group, while the expression of TIMP 1 and TIMP 2 did not differ between control and treatment groups. Conclusions: Compared to untreated controls, treatment with misoprostol was associated with a greater expression of inflammatory cells. It could be hypothesized that administration of misoprostol mimics the cervical ripening at term pregnancy by a possible influx and activation of inflammatory cells, which increases MMP 8 and MMP 9 and thereby leads to the degradation of collagen and cervical softening. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 39
页数:7
相关论文
共 30 条
[1]  
[Anonymous], 1981, CONTRACEPTION, V23, P251
[2]   Misoprostol for women's health: A review [J].
Blanchard, K ;
Clark, S ;
Winikoff, B ;
Gaines, G ;
Kabani, G ;
Shannon, C .
OBSTETRICS AND GYNECOLOGY, 2002, 99 (02) :316-332
[3]  
Bokstrom H, 1997, HUM REPROD, V12, P586
[4]  
BUSIEK DF, 1995, J IMMUNOL, V154, P6484
[5]   THE EFFECT OF MIFEPRISTONE (RU486) ON THE IMMUNOHISTOCHEMICAL DISTRIBUTION OF PROSTAGLANDIN-E AND ITS METABOLITE IN DECIDUAL AND CHORIONIC TISSUE IN EARLY-PREGNANCY [J].
CHENG, LN ;
KELLY, RW ;
THONG, KJ ;
HUME, R ;
BAIRD, DT .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (03) :873-877
[6]   CERVICAL DILATATION WITH 16,16-DIMETHYL-TRANS-DELTA-2-PGE1 METHYL-ESTER (CERVAGEM) PRIOR TO VACUUM ASPIRATION - A DOUBLE-BLIND, PLACEBO-CONTROLLED RANDOMIZED STUDY [J].
CHRISTENSEN, NJ ;
BYGDEMAN, M .
CONTRACEPTION, 1984, 29 (05) :457-464
[7]   CERVICAL RIPENING WITH THE CYTOKINES INTERLEUKIN-8, INTERLEUKIN-1-BETA AND TUMOR-NECROSIS-FACTOR-ALPHA IN GUINEA-PIGS [J].
CHWALISZ, K ;
BENSON, M ;
SCHOLZ, P ;
DAUM, J ;
BEIER, HM ;
HEGELEHARTUNG, C .
HUMAN REPRODUCTION, 1994, 9 (11) :2173-2181
[8]   Comparison between oral and vaginal administration of misoprostol on uterine contractility [J].
Danielsson, KG ;
Marions, L ;
Rodriguez, A ;
Spur, BW ;
Wong, PYK ;
Bygdeman, M .
OBSTETRICS AND GYNECOLOGY, 1999, 93 (02) :275-280
[9]   The effect of mifepristone administration on leukocyte populations, matrix metalloproteinases and inflammatory mediators in the first trimester cervix [J].
Denison, FC ;
Riley, SC ;
Elliott, CL ;
Kelly, RW ;
Calder, AA ;
Critchley, HOD .
MOLECULAR HUMAN REPRODUCTION, 2000, 6 (06) :541-548
[10]   Matrix metalloproteinases as mediators of reproductive function [J].
Hulboy, DL ;
Rudolph, LA ;
Matrisian, LM .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (01) :27-45