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Reproduction (Cambridge, England)2016; 151(5); 517-526; doi: 10.1530/REP-15-0617

Evidence for a PGF2α auto-amplification system in the endometrium in mares.

Abstract: In mares, prostaglandin F2α (PGF2α) secreted from the endometrium is a major luteolysin. Some domestic animals have an auto-amplification system in which PGF2α can stimulate its own production. Here, we investigated whether this is also the case in mares. In an in vivo study, mares at the mid-luteal phase (days 6-8 of estrous cycle) were injected i.m. with cloprostenol (250 µg) and blood samples were collected at fixed intervals until 72 h after treatment. Progesterone (P4) concentrations started decreasing 45 min after the injection and continued to decrease up to 24 h (P < 0.05). In turn, 13,14-dihydro-15-keto-PGF2α (PGFM) metabolite started to increase 4h after an injection and continued to increase up to 72 h (P < 0.05). PGF receptor (PTGFR) mRNA expression in the endometrium was significantly higher in the late luteal phase than in the early and regressed luteal phases (P < 0.05). In vitro, PGF2α significantly stimulated (P < 0.05) PGF2α production by endometrial tissues and endometrial epithelial and stromal cells and significantly increased (P < 0.05) the mRNA expression of prostaglandin-endoperoxide synthase-2 (PTGS2), an enzyme involved in PGF2α synthesis in endometrial cell. These findings strongly suggest the existence of an endometrial PGF2α auto-amplification system in mares.
Publication Date: 2016-02-23 PubMed ID: 26908917DOI: 10.1530/REP-15-0617Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article explores the possibility of an auto-amplification system in mares, where prostaglandin F2α (PGF2α), a hormone secreted by the endometrium (inner lining of the uterus), can stimulate its own production. The study includes both in-vivo and in-vitro experiments investigating this system, and the findings indicate a strong potential of the existence of PGF2α auto-amplification in mares.

Study Design and Methodology

  • The researchers conducted an in-vivo experiment where mares in the mid-luteal phase (days 6-8 of their estrous cycle) were injected with cloprostenol, a synthetic version of PGF2α. After the injection, the levels of progesterone (P4) and 13,14-dihydro-15-keto-PGF2α (PGFM, a metabolite of PGF2α) were measured over a 72-hour period.
  • An in-vitro study was also performed where PGF2α was used to stimulate endometrial tissue and cells to track the production of PGF2α and prostaglandin-endoperoxide synthase-2 (PTGS2) enzyme that contributes to the synthesis of PGF2α.

Results and Findings

  • The findings from the in-vivo study showed that progesterone levels started to decrease 45 minutes after constenol injection and continued to decrease up to 24 hours. Meanwhile, the PGFM metabolite started increasing 4 hours after the injection and continued to increase up to 72 hours.
  • The researchers also found that the expression of prostaglandin F receptor (PTGFR) mRNA in the endometrium was notably higher in the late luteal phase compared to both the early and regressed phases, indicating an increased production of PGF2α during that period.
  • In the in-vitro experiment, it was found that PGF2α notably stimulated the production of PGF2α by endometrial tissues and cells. It also increased the mRNA expression of PTGS2, the enzyme involved in PGF2α synthesis.
  • These findings strongly suggest the existence of a PGF2α auto-amplification system in the endometrium of mares, where PGF2α stimulates its own production.

Cite This Article

APA
Kozai K, Tokuyama S, Szóstek AZ, Toishi Y, Tsunoda N, Taya K, Sakatani M, Takahashi M, Nambo Y, Skarzynski DJ, Yamamoto Y, Kimura K, Okuda K. (2016). Evidence for a PGF2α auto-amplification system in the endometrium in mares. Reproduction, 151(5), 517-526. https://doi.org/10.1530/REP-15-0617

Publication

ISSN: 1741-7899
NlmUniqueID: 100966036
Country: England
Language: English
Volume: 151
Issue: 5
Pages: 517-526

Researcher Affiliations

Kozai, Keisuke
  • Laboratory of Reproductive PhysiologyGraduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
Tokuyama, Shota
  • Laboratory of Reproductive PhysiologyGraduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
Szóstek, Anna Z
  • Laboratory of Reproductive PhysiologyGraduate School of Environmental and Life Science, Okayama University, Okayama, Japan Department of Reproductive ImmunologyInstitute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Toishi, Yuko
  • Shadai CorporationHokkaido, Japan.
Tsunoda, Nobuo
  • Shadai CorporationHokkaido, Japan.
Taya, Kazuyoshi
  • Shadai CorporationHokkaido, Japan.
Sakatani, Miki
  • Kyushu Okinawa Agricultural Research CenterNational Agriculture and Food Research Organization (NARO), Kumamoto, Japan.
Takahashi, Masashi
  • Kyushu Okinawa Agricultural Research CenterNational Agriculture and Food Research Organization (NARO), Kumamoto, Japan Department of Animal ScienceHokkaido University, Hokkaido, Japan.
Nambo, Yasuo
  • Equine Science DivisionHidaka Training and Research Center, Japan Racing Association, Hokkaido, Japan Obihiro University of Agriculture and Veterinary MedicineObihiro, Japan.
Skarzynski, Dariusz J
  • Department of Reproductive ImmunologyInstitute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Yamamoto, Yuki
  • Laboratory of Reproductive PhysiologyGraduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
Kimura, Koji
  • Laboratory of Reproductive PhysiologyGraduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
Okuda, Kiyoshi
  • Laboratory of Reproductive PhysiologyGraduate School of Environmental and Life Science, Okayama University, Okayama, Japan Obihiro University of Agriculture and Veterinary MedicineObihiro, Japan kokuda@okayama-u.ac.jp.

MeSH Terms

  • Abortifacient Agents, Nonsteroidal / pharmacology
  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Corpus Luteum / drug effects
  • Corpus Luteum / metabolism
  • Dinoprost / analogs & derivatives
  • Dinoprost / blood
  • Dinoprost / pharmacology
  • Endometrium / drug effects
  • Endometrium / metabolism
  • Estrous Cycle / drug effects
  • Estrous Cycle / metabolism
  • Female
  • Horses
  • Progesterone / blood
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stromal Cells / drug effects
  • Stromal Cells / metabolism

Citations

This article has been cited 5 times.
  1. Piotrowska-Tomala KK, Jonczyk AW, Szóstek-Mioduchowska AZ, Żebrowska E, Ferreira-Dias G, Skarzynski DJ. The Effects of Prostaglandin E(2) Treatment on the Secretory Function of Mare Corpus Luteum Depends on the Site of Application: An in vivo Study. Front Vet Sci 2021;8:753796.
    doi: 10.3389/fvets.2021.753796pubmed: 35242830google scholar: lookup
  2. Rebordão MR, Amaral A, Fernandes C, Silva E, Lukasik K, Szóstek-Mioduchowska A, Pinto-Bravo P, Galvão A, Skarzynski DJ, Ferreira-Dias G. Enzymes Present in Neutrophil Extracellular Traps May Stimulate the Fibrogenic PGF(2α) Pathway in the Mare Endometrium. Animals (Basel) 2021 Sep 6;11(9).
    doi: 10.3390/ani11092615pubmed: 34573581google scholar: lookup
  3. Budik S, Walter I, Leitner MC, Ertl R, Aurich C. Expression of Enzymes Associated with Prostaglandin Synthesis in Equine Conceptuses. Animals (Basel) 2021 Apr 20;11(4).
    doi: 10.3390/ani11041180pubmed: 33924239google scholar: lookup
  4. Kikuchi K, Kozai K, Hojo T, Sakatani M, Okuda K, Bai H, Kawahara M, Takahashi M. Evaluating the electrical impedance and mucus-related gene expression of uterine endometrial tissues in mares. J Reprod Dev 2018 Apr 13;64(2):193-197.
    doi: 10.1262/jrd.2017-128pubmed: 29311525google scholar: lookup
  5. de Castro T, van Heule M, Domingues RR, Jacob JCF, Daels PF, Meyers SA, Conley AJ, Dini P. Embryo-endometrial interaction associated with the location of the embryo during the mobility phase in mares. Sci Rep 2024 Feb 7;14(1):3151.
    doi: 10.1038/s41598-024-53578-zpubmed: 38326534google scholar: lookup