Aronsson Annette, Ulfgren Ann-Kristin, Ståbi Berit, Stavreus-Evers Anneli, Gemzell-Danielsson Kristina
Department of Woman and Child Health, Division for Obstetrics and Gynecology, Karolinska Institute, S-171 76 Stockholm, Sweden.
Contraception. 2005 Jul;72(1):33-9. doi: 10.1016/j.contraception.2005.02.012.
The objective of the present study was to investigate the effect of vaginally and orally administered misoprostol on the local cervical inflammatory response.
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 mug, 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.
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.
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.
本研究的目的是调查经阴道和口服米索前列醇对局部宫颈炎症反应的影响。
将妊娠8至12周、因自愿要求行人工流产术而就诊的健康宫内妊娠妇女纳入一项队列研究,分为对照组和治疗组。在治疗组中,妇女被随机分为在手术前3小时口服或阴道给予400微克米索前列醇。在直接于机械性宫颈扩张和人工流产术前获取的宫颈活检组织中,评估CD45、CD68、基质金属蛋白酶8(MMP 8)、基质金属蛋白酶9(MMP 9)、金属蛋白酶组织抑制剂1(TIMP 1)和金属蛋白酶组织抑制剂2(TIMP 2)的免疫组织化学染色。
与对照组相比,治疗组宫颈上皮下区域CD45阳性细胞数量更多。两组CD68染色相似。治疗组MMP 8和MMP 9的免疫染色更强,而对照组和治疗组之间TIMP 1和TIMP 2的表达无差异。
与未治疗的对照组相比,米索前列醇治疗与炎症细胞表达增加有关。可以推测,米索前列醇的给药可能通过炎症细胞的可能流入和激活模拟足月妊娠时的宫颈成熟,这会增加MMP 8和MMP 9,从而导致胶原蛋白降解和宫颈软化。