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Reproduction (Cambridge, England)2002; 123(2); 261-268;

Prostaglandin E(2) and F(2 alpha) production by equine conceptuses and concentrations in conceptus fluids and uterine flushings recovered from early pregnant and dioestrous mares.

Abstract: A growing equine conceptus must suppress the cyclical release of PGF(2 alpha) from the endometrium to effect maternal recognition of its presence in the uterus. Paradoxically, the conceptus itself secretes PGF(2 alpha), together with other prostaglandins. In this study, the PGF(2 alpha) and PGE(2) content of, and production in vitro by, day 10-32 equine conceptuses were measured and the influence of pregnancy on the concentrations of these prostaglandins in the uterine lumen was examined. In vitro, the release of both prostaglandins per mg conceptus tissue was very high on day 10 after ovulation and lower thereafter. However, while PGF(2 alpha) production decreased further after day 18 of gestation, PGE(2) production remained high until day 32. Prostaglandin concentrations in yolk sac fluid were unaffected by gestational age and PGE(2) concentrations in this compartment were two to five times higher than PGF(2a) concentrations. PGF(2 alpha) concentrations reached high values in uterine flushings recovered from cyclic mares during days 14-16 after ovulation, the expected time of luteolysis, but were negligible in flushings recovered from pregnant mares at this time. Beyond day 18 of gestation, PGF(2 alpha) concentrations in uterine flushings were high and strikingly similar to those recorded during cyclical luteolysis. It is concluded that the equine conceptus effects maternal recognition of pregnancy primarily by inhibiting the ability of the endometrium to release PGF(2 alpha) during days 12-16 after ovulation. However, the conceptus appears to delay, rather than prevent, the development of the uterine PGF(2 alpha) release pathway and an alternative mechanism must prevent luteolysis from being triggered during days 18-32 of gestation.
Publication Date: 2002-02-28 PubMed ID: 11866693
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research explores the production of Prostaglandins, particularly Prostaglandin E(2) and F(2 alpha), by equine conceptuses and its subsequent influence on the concentrations in conceptus fluids and uterine flushings in pregnant and dioestrous mares. Notably, the study finds that the equine conceptus suppresses the release of PGF(2 alpha) from the endometrium for maternal recognition of pregnancy.

Investigation into Prostaglandin Production

  • The study performed measurements on the quantity and production process of PGF(2 alpha) and PGE(2) by equine conceptuses, with an age range from day 10 to day 32.
  • It was discovered that the release of both prostaglandins per milligram of conceptus tissue was extremely high on the 10th day after ovulation, and lower on the days following.
  • PGF(2 alpha) production experienced a further decrease after the 18th day of gestation, whereas, production of PGE(2) remained consistently high until day 32.

Prostaglandin Concentration in Various Components

  • The research examined the concentration of prostaglandins in yolk sac fluid, the uterine lumen, and uterine flushings.
  • Prostaglandin concentrations in yolk sac fluid were found to be stable, unaffected by gestational age. Interestingly, the concentrations of PGE(2) in this compartment were observed to be two to five times higher than the concentrations of PGF(2a).
  • When analyzing PGF(2 alpha) concentrations within uterine flushings recovered from cyclic mares during the 14-16 days after ovulation, the time of expected luteolysis, researchers observed high values. However, these high values were nonexistent in flushings collected from pregnant mares during this same timeframe.
  • After day 18 of gestation, PGF(2 alpha) concentrations in uterine flushings were high, notably similar to concentrations identified during cyclical luteolysis.

Findings and Conclusion

  • The results suggest that the equine conceptus primarily affects maternal recognition of pregnancy by inhibiting the ability of the endometrium to release PGF(2 alpha) from days 12-16 after ovulation.
  • The conceptus seems to delay the development of the uterine PGF(2 alpha) release pathway, rather than prevent its initiation. However, the researchers propose that there must be an alternative mechanism which prevents luteolysis from being activated between days 18-32 of gestation.

Cite This Article

APA
Stout TA, Allen WR. (2002). Prostaglandin E(2) and F(2 alpha) production by equine conceptuses and concentrations in conceptus fluids and uterine flushings recovered from early pregnant and dioestrous mares. Reproduction, 123(2), 261-268.

Publication

ISSN: 1470-1626
NlmUniqueID: 100966036
Country: England
Language: English
Volume: 123
Issue: 2
Pages: 261-268

Researcher Affiliations

Stout, T A E
  • TBA Equine Fertility Unit, Mertoun Paddocks, Woodditton Road, Newmarket CB8 9BH, UK. T.A.E.Stout@vet.uu.nl
Allen, W R

    MeSH Terms

    • Animals
    • Blastocyst / metabolism
    • Corpus Luteum Maintenance
    • Dinoprost / analysis
    • Dinoprost / biosynthesis
    • Dinoprostone / analysis
    • Dinoprostone / biosynthesis
    • Female
    • Gestational Age
    • Horses / metabolism
    • Pregnancy
    • Radioimmunoassay / methods
    • Uterus / metabolism

    Citations

    This article has been cited 13 times.
    1. Newcombe JR, Cuervo-Arango J, Wilsher S. The Timing of the Maternal Recognition of Pregnancy Is Specific to Individual Mares.. Animals (Basel) 2023 May 22;13(10).
      doi: 10.3390/ani13101718pubmed: 37238148google scholar: lookup
    2. Vegas AR, Podico G, Canisso IF, Bollwein H, Fröhlich T, Bauersachs S, Almiñana C. Dynamic regulation of the transcriptome and proteome of the equine embryo during maternal recognition of pregnancy.. FASEB Bioadv 2022 Dec;4(12):775-797.
      doi: 10.1096/fba.2022-00063pubmed: 36479207google scholar: lookup
    3. Diel de Amorim M, Klein C, Foster R, Dong L, Lopez-Rodriguez MF, Card C. Expression of Oxytocin/Neurophysin I and Oxytocinase in the Equine Conceptus from Day 8 to Day 21 Post-Ovulation.. Animals (Basel) 2022 Mar 22;12(7).
      doi: 10.3390/ani12070799pubmed: 35405789google scholar: lookup
    4. Lawson EF, Grupen CG, Baker MA, Aitken RJ, Swegen A, Pollard CL, Gibb Z. Conception and early pregnancy in the mare: lipidomics the unexplored frontier.. Reprod Fertil 2022 Jan 1;3(1):R1-R18.
      doi: 10.1530/RAF-21-0104pubmed: 35350651google scholar: lookup
    5. Rivera Del Alamo MM, Reilas T, Lukasik K, Galvão AM, Yeste M, Katila T. Inflammatory Markers in Uterine Lavage Fluids of Pregnant, Non-Pregnant, and Intrauterine Device Implanted Mares on Days 10 and 15 Post Ovulation.. Animals (Basel) 2021 Dec 8;11(12).
      doi: 10.3390/ani11123493pubmed: 34944269google scholar: lookup
    6. Rudolf Vegas A, Podico G, Canisso IF, Bollwein H, Almiñana C, Bauersachs S. Spatiotemporal endometrial transcriptome analysis revealed the luminal epithelium as key player during initial maternal recognition of pregnancy in the mare.. Sci Rep 2021 Nov 16;11(1):22293.
      doi: 10.1038/s41598-021-01785-3pubmed: 34785745google scholar: lookup
    7. Klein C, Bruce P, Hammermueller J, Hayes T, Lillie B, Betteridge K. Transcriptional profiling of equine endometrium before, during and after capsule disintegration during normal pregnancy and after oxytocin-induced luteostasis in non-pregnant mares.. PLoS One 2021;16(10):e0257161.
      doi: 10.1371/journal.pone.0257161pubmed: 34614002google scholar: lookup
    8. Swegen A. Maternal recognition of pregnancy in the mare: does it exist and why do we care?. Reproduction 2021 May 5;161(6):R139-R155.
      doi: 10.1530/REP-20-0437pubmed: 33957605google scholar: lookup
    9. Gibson C, de Ruijter-Villani M, Bauersachs S, Stout TAE. Asynchronous Embryo Transfer Followed by Comparative Transcriptomic Analysis of Conceptus Membranes and Endometrium Identifies Processes Important to the Establishment of Equine Pregnancy.. Int J Mol Sci 2020 Apr 7;21(7).
      doi: 10.3390/ijms21072562pubmed: 32272720google scholar: lookup
    10. Smits K, Gansemans Y, Tilleman L, Van Nieuwerburgh F, Van De Velde M, Gerits I, Ververs C, Roels K, Govaere J, Peelman L, Deforce D, Van Soom A. Maternal Recognition of Pregnancy in the Horse: Are MicroRNAs the Secret Messengers?. Int J Mol Sci 2020 Jan 9;21(2).
      doi: 10.3390/ijms21020419pubmed: 31936511google scholar: lookup
    11. Bonometti S, Menarim BC, Reinholt BM, Ealy AD, Johnson SE. Growth factor modulation of equine trophoblast mitosis and prostaglandin gene expression.. J Anim Sci 2019 Feb 1;97(2):865-873.
      doi: 10.1093/jas/sky473pubmed: 30535412google scholar: lookup
    12. Aurich C, Budik S. Early pregnancy in the horse revisited - does exception prove the rule?. J Anim Sci Biotechnol 2015;6:50.
      doi: 10.1186/s40104-015-0048-6pubmed: 26635959google scholar: lookup
    13. Tachibana Y, Sakurai T, Bai H, Shiota K, Nambo Y, Nagaoka K, Imakawa K. RNA-seq analysis of equine conceptus transcripts during embryo fixation and capsule disappearance.. PLoS One 2014;9(12):e114414.
      doi: 10.1371/journal.pone.0114414pubmed: 25514169google scholar: lookup