Endometrial steroid receptors during decidualization in rhesus monkey (Macaca mulatta);: their modulation by anti-oestrogen CDRI-85/287

被引:10
作者
Dwivedi, A [1 ]
Bansode, FW [1 ]
Setty, BS [1 ]
Dhar, JD [1 ]
机构
[1] Cent Drug Res Inst, Div Endocrinol, Lucknow 226001, Uttar Pradesh, India
关键词
anti-oestrogen; decidualization; endometrium; receptors;
D O I
10.1093/humrep/14.4.1090
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
With a view to elucidating the hormonal control of decidualization in rhesus monkey, we studied the effects of CDRI-85/287, a potent anti-oestrogen, on endometrial steroid receptors in viva and in vitro. Compound 85/287 was administered (i.m.) on days 8, 9 and 10 of steroid treatment cycle at a dose of 15 mg/monkey. Deciduoma was induced on day 16. Histological examination of endometrial tissue on days 24 and 30 of the cycle showed an apparent inhibition in uterine epithelial and subepithelial decidual cell plaque formation and a decrease in leukocytic infiltration into the stroma in anti-oestrogen-treated animals. As observed on day 24 a significant decrease in progesterone receptors (PR) (nuclear + cytosolic) was observed in the 85/287-treated group, whereas oestrogen receptor (ER) content remained unaltered. On day 30 total ER as well as total PR content was markedly reduced in treated animals, In-vitro results clearly demonstrated a competitive antagonism of 85/287 at the ER level only, The results are discussed in relation to the histological changes and modulation of steroid receptors, thereby suggesting the decidualization inhibitory activity of anti-oestrogen molecule 85/287 in primate species.
引用
收藏
页码:1090 / 1095
页数:6
相关论文
共 41 条
[21]   PATTERNS OF ESTROGEN AND PROGESTERONE RECEPTORS IN MONKEY ENDOMETRIUM DURING THE NORMAL MENSTRUAL-CYCLE [J].
KREITMANNGIMBAL, B ;
BAYARD, F ;
NIXON, WE ;
HODGEN, GD .
STEROIDS, 1980, 35 (04) :471-479
[22]  
LESSEY BA, 1989, FERTIL STERIL, V51, P409
[23]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[24]  
MacGregor JI, 1998, PHARMACOL REV, V50, P151
[25]   Differential expression of uterine progesterone receptor forms A and B during the menstrual cycle [J].
Mangal, RK ;
Wiehle, RD ;
Poindexter, AN ;
Weigel, NL .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 63 (4-6) :195-202
[26]   Binding characteristics of novel nonsteroidal antiestrogens to the rat uterine estrogen receptors [J].
Martel, C ;
Provencher, L ;
Li, X ;
St Pierre, A ;
Leblanc, G ;
Gauthier, S ;
Mérand, Y ;
Labrie, F .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1998, 64 (3-4) :199-205
[27]   The two native estrogen receptor forms of 8S and 4S present in cytosol from human uterine tissues display opposite reactivities with the antiestrogen tamoxifen aziridine and the estrogen responsive element [J].
Navarro, D ;
Leon, L ;
Chirino, R ;
Fernández, L ;
Pestano, J ;
Diaz-Chico, BN .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1998, 64 (1-2) :49-58
[28]  
Neulen J, 1996, HUM REPROD, V11, P1533
[29]  
OKULICZ WC, 1990, FERTIL STERIL, V53, P913
[30]   SUBCELLULAR-DISTRIBUTION OF ANDROGENS AND ESTROGENS IN TARGET TISSUE [J].
POORTMAN, J ;
THIJSSEN, JHH ;
VANLANDEGHEM, AAJ ;
WIEGERINCK, MAHM ;
ALSBACH, GPJ .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1983, 19 (01) :939-945