» Articles » PMID: 33827696

Pre-implantation Exogenous Progesterone and Pregnancy in Sheep. II. Effects on Fetal-placental Development and Nutrient Transporters in Late Pregnancy

Overview
Publisher Biomed Central
Date 2021 Apr 8
PMID 33827696
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Administration of progesterone (P4) to ewes during the first 9 to 12 days of pregnancy accelerates blastocyst development by day 12 of pregnancy, likely due to P4-induced up-regulation of key genes in uterine epithelia responsible for secretion and transport of components of histotroph into the uterine lumen. This study determined if acceleration of blastocyst development induced by exogenous P4 during the pre-implantation period affects fetal-placental development on day 125 of pregnancy. Suffolk ewes (n = 35) were mated to fertile rams and assigned randomly to receive daily intramuscular injections of either corn oil vehicle (CO, n = 18) or 25 mg progesterone in CO (P4, n = 17) for the first 8 days of pregnancy. All ewes were hysterectomized on day 125 of pregnancy and: 1) fetal and placental weights and measurements were recorded; 2) endometrial and placental tissues were analyzed for the expression of candidate mRNAs involved in nutrient transport and arginine metabolism; and 3) maternal plasma, fetal plasma, allantoic fluid, and amniotic fluid were analyzed for amino acids, agmatine, polyamines, glucose, and fructose.

Results: Treatment of ewes with exogenous P4 did not alter fetal or placental growth, but increased amounts of aspartate and arginine in allantoic fluid and amniotic fluid, respectively. Ewes that received exogenous P4 had greater expression of mRNAs for SLC7A1, SLC7A2, SLC2A1, AGMAT, and ODC1 in endometria, as well as SLC1A4, SLC2A5, SLC2A8 and ODC1 in placentomes. In addition, AZIN2 protein was immunolocalized to uterine luminal and glandular epithelia in P4-treated ewes, whereas AZIN2 localized only to uterine luminal epithelia in CO-treated ewes.

Conclusions: This study revealed that exogenous P4 administered in early pregnancy influenced expression of selected genes for nutrient transporters and the expression of a protein involved in polyamine synthesis on day 125 of pregnancy, suggesting a 'programming' effect of P4 on gene expression that affected the composition of nutrients in fetal-placental fluids.

Citing Articles

Exogenous progesterone supplementation: a strategy to enhance conceptus development in sheep and pigs?.

Tyree M, Stenhouse C Reprod Fertil. 2024; 6(1).

PMID: 39700015 PMC: 11877642. DOI: 10.1530/RAF-24-0092.


Early Embryonic Development in Agriculturally Important Species.

Bazer F, Johnson G Animals (Basel). 2024; 14(13).

PMID: 38997994 PMC: 11240814. DOI: 10.3390/ani14131882.


Progesterone regulates tissue non-specific alkaline phosphatase (TNSALP) expression and activity in ovine utero-placental tissues.

Stenhouse C, Halloran K, Hoskins E, Moses R, Wu G, Seo H J Anim Sci Biotechnol. 2024; 15(1):90.

PMID: 38956701 PMC: 11220967. DOI: 10.1186/s40104-024-01048-x.


Concentrations of vitamin B12 and folate in maternal serum and fetal fluids, metabolite interrelationships, and hepatic transcript abundance of key folate and methionine cycle genes: the impacts of maternal nutrition during the first 50 d of....

Syring J, Crouse M, Neville T, Ward A, Dahlen C, Reynolds L J Anim Sci. 2023; 101.

PMID: 37129588 PMC: 10199783. DOI: 10.1093/jas/skad139.


Phosphate, calcium, and vitamin D signaling, transport, and metabolism in the endometria of cyclic ewes.

Stenhouse C, Newton M, Halloran K, Moses R, Sah N, Suva L J Anim Sci Biotechnol. 2023; 14(1):13.

PMID: 36631878 PMC: 9835233. DOI: 10.1186/s40104-022-00803-2.


References
1.
Enders A, Carter A . Comparative placentation: some interesting modifications for histotrophic nutrition -- a review. Placenta. 2006; 27 Suppl A:S11-6. DOI: 10.1016/j.placenta.2005.10.013. View

2.
Wen H, Abbasi S, Kellems R, Xia Y . mTOR: a placental growth signaling sensor. Placenta. 2005; 26 Suppl A:S63-9. DOI: 10.1016/j.placenta.2005.02.004. View

3.
Fozard J, Part M, Prakash N, Grove J, Schechter P, SJOERDSMA A . L-Ornithine decarboxylase:an essential role in early mammalian embryogenesis. Science. 1980; 208(4443):505-8. DOI: 10.1126/science.6768132. View

4.
White C, Piper E, Noland P . Conversion of glucose to fructose in the fetal pig. J Anim Sci. 1979; 48(3):585-90. DOI: 10.2527/jas1979.483585x. View

5.
Marconi A, Cetin I, Davoli E, Baggiani A, Fanelli R, Fennessey P . An evaluation of fetal glucogenesis in intrauterine growth-retarded pregnancies. Metabolism. 1993; 42(7):860-4. DOI: 10.1016/0026-0495(93)90060-2. View