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Canine placenta: a source of prepartal prostaglandins during normal and antiprogestin-induced parturition.
- Source :
-
Reproduction (Cambridge, England) [Reproduction] 2010 Mar; Vol. 139 (3), pp. 655-64. Date of Electronic Publication: 2009 Nov 24. - Publication Year :
- 2010
-
Abstract
- Expression of cyclooxygenase 2 (COX2, now known as PTGS2), prostaglandin E2 synthase (PTGES, PGES), and prostaglandin F2alpha synthase (PGFS), of the respective receptors PTGFR (FP), PTGER2 (EP2), and PTGER4 (EP4) and of the progesterone receptor (PGR, PR) was assessed by real-time PCR, immunohistochemistry (IHC), or in situ hybridization (ISH) in utero/placental tissue samples collected from three to five bitches on days 8-12 (pre-implantation), 18-25 (post-implantation), and 35-40 (mid-gestation) of pregnancy and during the prepartal luteolysis. Additionally, ten mid-pregnant bitches were treated with the antiprogestin aglepristone (10 mg/kg bw (2x/24 h)); ovariohysterectomy was 24 and 72 h after the second treatment. Plasma progesterone and 15-ketodihydro-PGF2alpha (PGFM) concentrations were determined by RIA. Expression of the PGR was highest before implantation and primarily located to the endometrium; expression in the placenta was restricted to the decidual cells. PTGS2 was constantly low expressed until mid-gestation; a strong upregulation occurred at prepartal luteolysis concomitant with an increase in PGFM. PGFS was upregulated after implantation and significantly elevated through early and mid-gestation. PTGES showed a gradual increase and a strong prepartal upregulation. PTGFR, PTGER2, and PTGER4 were downregulated after implantation; a gradual upregulation of PTGFR and PTGER2 occurred towards parturition. ISH and IHC co-localized PGFS, PTGFR, PTGES, and PTGS2 in the trophoblast and endometrium. The changes following application of aglepristone were in the same direction as those observed from mid-gestation to prepartal luteolysis. These data suggest that the prepartal increase of PGF2alpha results from a strong upregulation of PTGS2 in the fetal trophoblast with the withdrawal of progesterone having a signalling function and the decidual cells playing a key role in the underlying cell-to-cell crosstalk.
- Subjects :
- Animals
Dinoprost blood
Dinoprost metabolism
Estrenes pharmacology
Female
Gestational Age
Hormone Antagonists pharmacology
Oxytocics pharmacology
Parturition blood
Parturition drug effects
Parturition physiology
Placenta drug effects
Placenta physiology
Pregnancy
Progesterone blood
Progesterone metabolism
Progesterone Congeners pharmacology
Prostaglandin-Endoperoxide Synthases genetics
Prostaglandin-Endoperoxide Synthases metabolism
Receptors, Prostaglandin genetics
Receptors, Prostaglandin metabolism
Dogs metabolism
Dogs physiology
Labor, Induced methods
Labor, Induced veterinary
Parturition metabolism
Placenta metabolism
Pregnancy, Animal blood
Pregnancy, Animal metabolism
Prostaglandins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1741-7899
- Volume :
- 139
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Reproduction (Cambridge, England)
- Publication Type :
- Academic Journal
- Accession number :
- 19934344
- Full Text :
- https://doi.org/10.1530/REP-09-0140