JME
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Journal of Molecular Endocrinology (1995) 14, 237-245    DOI: 10.1677/jme.0.0140237
© 1995 Society for Endocrinology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rice, G E
Right arrow Articles by Jacobs, R A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rice, G E
Right arrow Articles by Jacobs, R A

Gestational- and labour-associated changes in the relative abundance of prostaglandin G/H synthase-1 and -2 mRNA in ovine placenta

G E Rice, K A Freed, M A Aitken and R A Jacobs

The aim of this study was to establish the gestational- and labour-associated variation in the relative abundance of prostaglandin synthase-1 (PGHS-1) and prostaglandin synthase-2 (PGHS-2) mRNA in ovine placenta (cotyledons). Cotyledons were collected from non-labouring ewes at 40–145 days of gestation (n=25) and from ewes in active labour (145–147 days, n=5). The relative abundance of PGHS-1 and PGHS-2 mRNA transcripts was determined by Northern blot analysis and laser densitometry, using a 2·3 kb sheep and a 1·2kb mouse cDNA probe respectively. Data were expressed as a ratio of PGHS transcript hybridization/18S rRNA hybridization. During pregnancy, the relative abundance of PGHS-2 mRNA increased sevenfold, from 0·19±0·04 at 40–85 days (n=5) to 1·39±0·05 at 140–145 days (n=4) (P<0·01). PGHS-1 mRNA relative abundance did not change significantly (P>0·05) during gestation. Neither PGHS-1 nor PGHS-2 mRNA relative abundance changed significantly in association with labour onset at term (n=5) when compared with the relative abundance observed at 140–145 days (n=4) (P>0·05). The data obtained in this study are consistent with the hypothesis that PGHS-1 is constitutively expressed in ovine placenta during pregnancy and at the time of labour, and that PGHS-2 is induced during the second half of pregnancy. It remains to be established to what extent these two isozymes contribute to the net prostaglandin-forming capacity of the ovine placenta, particularly at the time of labour.




This article has been cited by other articles:


Home page
J Mol EndocrinolHome page
Q. Zhang and W. X. Wu
Separate and synergistic effect of progesterone and estradiol on induction of annexin 2 and its interaction protein p11 in pregnant sheep myometrium
J. Mol. Endocrinol., April 1, 2007; 38(4): 441 - 454.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
Q. Zhang, V. Collins, K. Chakrabarty, R. F. Wolf, N. Unno, D. Howe, J. C. Rose, and W. X. Wu
Regulation of Membrane-Associated Prostaglandin E2 Synthase 1 in Pregnant Sheep Intrauterine Tissues by Glucocorticoid and Estradiol
Endocrinology, August 1, 2006; 147(8): 3719 - 3726.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
H. K. Palliser, J. J. Hirst, G. E. Rice, G. T. Ooi, N. L. Dellios, R. M. Escalona, and I. R. Young
Labor-Associated Regulation of Prostaglandin E and F Synthesis and Action in the Ovine Amnion and Cervix
Reproductive Sciences, January 1, 2006; 13(1): 19 - 24.
[Abstract] [PDF]


Home page
EndocrinologyHome page
W. X. Wu, X. H. Ma, T. Coksaygan, K. Chakrabarty, V. Collins, J. Rose, and P. W. Nathanielsz
Prostaglandin Mediates Premature Delivery in Pregnant Sheep Induced by Estradiol at 121 Days of Gestational Age
Endocrinology, March 1, 2004; 145(3): 1444 - 1452.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
J. A. Arosh, S. K. Banu, P. Chapdelaine, and M. A. Fortier
Temporal and Tissue-Specific Expression of Prostaglandin Receptors EP2, EP3, EP4, FP, and Cyclooxygenases 1 and 2 in Uterus and Fetal Membranes during Bovine Pregnancy
Endocrinology, January 1, 2004; 145(1): 407 - 417.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
R.L. Martin, W.L. Whittle, A.C. Holloway, S. Gyomorey, W. Gibb, S. Lye, and J.R.G. Challis
Ontogeny and Regulation of Ovine Placental Prostaglandin E2 Synthase
Biol Reprod, September 1, 2002; 67(3): 868 - 873.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
W. X. Wu, X. H. Ma, N. Unno, and P. W. Nathanielsz
In Vivo Evidence for Stimulation of Placental, Myometrial, and Endometrial Prostaglandin G/H Synthase 2 by Fetal Cortisol Replacement after Fetal Adrenalectomy
Endocrinology, September 1, 2001; 142(9): 3857 - 3864.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
J. R.G. Challis, S. G. Matthews, W. Gibb, and S. J. Lye
Endocrine and Paracrine Regulation of Birth at Term and Preterm
Endocr. Rev., October 1, 2000; 21(5): 514 - 550.
[Abstract] [Full Text]


Home page
EndocrinologyHome page
J. L. Cook, D. B. Zaragoza, D. H. Sung, and D. M. Olson
Expression of Myometrial Activation and Stimulation Genes in a Mouse Model of Preterm Labor: Myometrial Activation, Stimulation, and Preterm Labor
Endocrinology, May 1, 2000; 141(5): 1718 - 1728.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
S. Gyomorey, S.J. Lye, W. Gibb, and J.R.G. Challis
Fetal-to-Maternal Progression of Prostaglandin H2 Synthase-2 Expression in Ovine Intrauterine Tissues During the Course of Labor
Biol Reprod, March 1, 2000; 62(3): 797 - 805.
[Abstract] [Full Text]


Home page
EndocrinologyHome page
G. Charpigny, P. Reinaud, J.-P. Tamby, C. Creminon, J. Martal, J. Maclouf, and M. Guillomot
Expression of Cyclooxygenase-1 and -2 in Ovine Endometrium During the Estrous Cycle and Early Pregnancy
Endocrinology, May 1, 1997; 138(5): 2163 - 2171.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1995 by the Society for Endocrinology.