Human cervical ripening is associated with an increase in cervical inducible nitric oxide synthase expression

被引:72
作者
Tschugguel, W
Schneeberger, C
Lass, H
Stonek, F
Zaghlula, MB
Czerwenka, K
Schatten, C
Kaider, A
Husslein, P
Huber, JC
机构
[1] Univ Vienna, Sch Med,AKH, Dept Obstet & Gynecol, Div Gynecol Endocrinol & Reprod Med, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Clin Pathol, A-1090 Vienna, Austria
[3] Univ Vienna, Dept Med Comp Sci, A-1090 Vienna, Austria
关键词
D O I
10.1095/biolreprod60.6.1367
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mechanisms that ultimately regulate cervical ripening during parturition remain largely unknown. A possible role for nitric oxide (NO) has recently emerged; however, the expression of NO synthase (NOS) within the human cervix in the ripening process has not been investigated. The purpose of this study was to identify cell types in the human cervix that contain NOS isoforms and to examine changes in their expression during the ripening process and the nonpregnant state. Inducible NOS (iNOS) immunoreactivity was observed in the epithelial cells and stromal spindle cells in 17 of 20 biopsies from cervices obtained within 10 min postpartum, but in only 4 of 12 nonpregnant controls (p 0.03). Endothelial NOS (eNOS) immunoreactivity was restricted to vascular endothelia in all sections, whereas neuronal NOS was not detectable. Inducible NOS activity in the postpartum group was 3.2 times that of the central group (p = 0.0005), whereas constitutive NOS activity remained unchanged in both groups (p = 0.222). Competitive reverse transcription-polymerase chain reaction revealed no differences in the expression of iNOS (p = 0.443) or eNOS mRNA (p = 0.409). The existence of iNOS in the human postpartum cervix suggests that increased production of NO, probably induced by cytokines, may be relevant to the process of natural cervical ripening in humans.
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页码:1367 / 1372
页数:6
相关论文
共 37 条
[1]   Changes in expression of the nitric oxide synthase isoforms in rat uterus and cervix during pregnancy and parturition [J].
Ali, M ;
Buhimschi, I ;
Chwalisz, K ;
Garfield, RE .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (11) :995-1003
[2]  
Bokstrom H, 1997, HUM REPROD, V12, P586
[3]  
Buhimschi I, 1996, HUM REPROD, V11, P1755
[4]  
CALDER AA, 1992, RECENT ADV OBSTET GY, V17, P33
[5]   CLONING, CHARACTERIZATION, AND EXPRESSION OF A CDNA-ENCODING AN INDUCIBLE NITRIC-OXIDE SYNTHASE FROM THE HUMAN CHONDROCYTE [J].
CHARLES, IG ;
PALMER, RMJ ;
HICKERY, MS ;
BAYLISS, MT ;
CHUBB, AP ;
HALL, VS ;
MOSS, DW ;
MONCADA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) :11419-11423
[6]   Immunocytochemical localization of nitric oxide synthase-III in reproductive organs of female rats during the oestrous cycle [J].
Chatterjee, S ;
Gangula, PRR ;
Dong, YL ;
Yallampalli, C .
HISTOCHEMICAL JOURNAL, 1996, 28 (10) :715-723
[7]   Cervical ripening in guinea-pigs after a local application of nitric oxide [J].
Chwalisz, K ;
Shao-Qing, S ;
Garfield, RE ;
Beier, HM .
HUMAN REPRODUCTION, 1997, 12 (10) :2093-2101
[8]   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
[9]  
CHWALISZ K, 1996, PRENAT NEONAT MED, V1, P292
[10]   UTERINE HYPERSTIMULATION AFTER LOW-DOSE PROSTAGLANDIN-E2 THERAPY - TOCOLYTIC TREATMENT IN 181 CASES [J].
EGARTER, CH ;
HUSSLEIN, PW ;
RAYBURN, WF .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1990, 163 (03) :794-796