PROSTAGLANDIN ENDOPEROXIDE-H SYNTHASE (PGHS) ACTIVITY AND IMMUNOREACTIVE PGHS-1 AND PGHS-2 LEVELS IN HUMAN AMNION THROUGHOUT GESTATION, AT TERM, AND DURING LABOR

被引:110
作者
TEIXEIRA, FJ
ZAKAR, T
HIRST, JJ
GUO, F
SADOWSKY, DW
MACHIN, G
DEMIANCZUK, N
RESCH, B
OLSON, DM
机构
[1] UNIV ALBERTA, PERINATAL RES CTR, DEPT OBSTET & GYNECOL, EDMONTON T6G 2S2, AB, CANADA
[2] UNIV ALBERTA, DEPT PATHOL, EDMONTON T6G 2S2, AB, CANADA
[3] UNIV ALBERTA, DEPT PEDIAT, EDMONTON T6G 2S2, AB, CANADA
[4] UNIV ALBERTA, DEPT PHYSIOL, EDMONTON T6G 2S2, AB, CANADA
[5] UNIV SZEGED, SCH MED, DEPT OBSTET & GYNECOL, SZEGED, HUNGARY
关键词
D O I
10.1210/jc.78.6.1396
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prostaglandins (PGs) are of primary importance in the initiation and maintenance of labor in women. A major intrauterine source of prostaglandins is the amnion, which synthesizes increased amounts of PGE(2) at term labor. Because PG endoperoxide-H synthase (PGHS) catalyzes the rate-limiting step of PG synthesis from arachidonic acid, we investigated the changes in amniotic PGHS specific activity during gestation and at term and preterm labor. Also, we determined the level of immunoreactive PGHS protein in the amnion to evaluate the mechanisms by which PGHS activity may be regulated. PGHS specific activity, measured as the amount of PGE(2) produced by amnion microsomes under optimal conditions, was 18.2 +/- 3.7 pg PGE(2)/mu g protein.min (mean +/- SE; n = 19) at term (37-42 weeks gestation) before the spontaneous onset of labor. PGHS specific activity was significantly higher after spontaneous term labor (38.9 +/- 6.0 pg PGE(2)/mu g protein.min; n = 19; P < 0.05). Amnion samples from preterm (<36 weeks gestation) nonlaboring patients contained low levels of PGHS specific activity (5.9 +/- 1.8 pg PGE(2)/mu g protein.min; n = 9), which increased significantly with spontaneous preterm labor (28.3 +/- 6.8 pg PGE(2)/mu g protein.min; n = 10; P < 0.05). Longitudinal analysis of the data showed that PGHS specific activity was low in the first and second trimesters of gestation, but increased dramatically before labor onset at term. We detected PGHS protein in all microsomal samples, with an antiovine PGHS antibody recognizing both PGHS-1 and -2 isoforms of the enzyme. However, there was no correlation between PGHS specific activity and the amount of immunoreactive PGHS protein. Using an antibody specific for PGHS-2, we detected immunoreactive protein in only 9 of the 25 tissues examined and found no correlation between PGHS specific activity and the amount of PGHS-2 protein. These results suggest that 1) PGHS specific activity in the amnion increases sharply before the onset of labor at term; 2) further increases in specific activity occur during term and preterm labor; and 3) the specific activity of PGHS in the amnion is not related directly to the amount of immunoreactive enzyme protein.
引用
收藏
页码:1396 / 1402
页数:7
相关论文
共 29 条
[1]   CHANGES IN EXPRESSION OF THE CYCLOOXYGENASE GENE IN HUMAN FETAL MEMBRANES AND PLACENTA WITH LABOR [J].
BENNETT, PR ;
HENDERSON, DJ ;
MOORE, GE .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (01) :212-216
[2]  
BLEASDALE JE, 1989, FETAL MED REV, P242
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]  
Challis J.R.G., 1988, P2177
[5]   PROSTAGLANDIN ENDOPEROXIDE SYNTHASE - REGULATION OF ENZYME EXPRESSION [J].
DEWITT, DL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1083 (02) :121-134
[6]   ARACHIDONIC-ACID METABOLISM BY RABBIT FETAL MEMBRANES OF VARIOUS GESTATIONAL AGES [J].
ELLIOTT, WJ ;
MCLAUGHLIN, LL ;
BLOCH, MH ;
NEEDLEMAN, P .
PROSTAGLANDINS, 1984, 27 (01) :27-36
[7]   PERSISTENT INDUCTION OF CYCLOOXYGENASE IN P60V-SRC-TRANSFORMED 3T3 FIBROBLASTS [J].
HAN, JW ;
SADOWSKI, H ;
YOUNG, DA ;
MACARA, IG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3373-3377
[8]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[9]   ENDOGENOUS GLUCOCORTICOIDS REGULATE AN INDUCIBLE CYCLOOXYGENASE ENZYME [J].
MASFERRER, JL ;
SEIBERT, K ;
ZWEIFEL, B ;
NEEDLEMAN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) :3917-3921
[10]  
MITCHELL MD, 1988, ONSET LABOR CELLULAR, P165