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Theriogenology2021; 173; 221-229; doi: 10.1016/j.theriogenology.2021.08.009

Effects of cortisol on prostaglandin F2α secretion and expression of genes involved in the arachidonic acid metabolic pathway in equine endometrium – In vitro study.

Abstract: Glucocorticoids (GCs) are known to play an important role in maintaining basal and stress-related homeostasis by interacting with endocrine mediators and prostaglandins (PGs). Although a growing body of evidence shows that GCs exert their regulatory action at a multitude of sites in the reproductive axis through corticosteroid receptors, little is known about the direct role of cortisol, an active form of GCs, in the equine endometrium. Thus, the study aimed to determine the effect of cortisol on PGF synthesis in the endometrial tissue and cells in vitro. In Exp.1, the immunolocalization and the expression of the glucocorticoid receptor (GCR) in the endometrium throughout the estrous cycle were established. In Exp. 2 and 3, the effects of cortisol on PGF secretion and transcripts associated with the arachidonic acid (AA) cascade in endometrial tissues, and cells were defined. Endometrial tissues obtained from the early, mid, and late luteal phases and the follicular phase of the estrous cycle were exposed to cortisol (100, 200, and 400 nM) for 24 h. Endometrial epithelial and stromal cells (early phase of estrous cycle) were exposed to cortisol (100 nM) for 24 h. Then, PGF secretion and transcripts associated with the AA cascade (PLA2G2A, PLA2G4A, PTGS2, and PGFS) were assessed. GCR was expressed in the cytoplasm and the nucleus in the luminal and glandular epithelium as well as in the stroma. Endometrial GCR protein abundance was up-regulated at the late luteal phase compared to the mid-luteal phase of the estrous cycle. Cortisol dose-dependently decreased PGF secretion, PLA2G2A and PLA2G4A transcripts in endometrial tissues. Additionally, cortisol treatment decreased PGF secretion from endometrial epithelial and stromal cells. Moreover, it affected PLA2G2A, PLA2G4A, and PTGS2 transcripts in endometrial stromal cells. These findings suggest that cortisol suppresses the synthesis of PGF by affecting the AA cascade in the equine endometrium during the estrous cycle.
Publication Date: 2021-08-08 PubMed ID: 34399386DOI: 10.1016/j.theriogenology.2021.08.009Google Scholar: Lookup
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  • Journal Article

Summary

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This research paper focuses on the study of the impact of cortisol, an active form of glucocorticoids, on prostaglandin synthesis in the endometrial tissue and cells of horses. The results show that cortisol appears to suppress the production of prostaglandin by affecting the arachidonic acid (AA) cascade in the equine endometrium during the estrous cycle.

Study Objectives and Design

  • The primary aim of the study was to investigate how cortisol impacts prostaglandin F (PGF) synthesis in horse endometrial tissue and cells using in vitro methods.
  • The research was divided into 3 experiments. The first established the presence and expression level of the glucocorticoid receptor (GCR) in the endometrial tissue during the estrous cycle.
  • The second and third experiments explored how cortisol affects PGF secretion, as well as the expression of genes associated with the AA cascade, in both endometrial tissues and cells.

Methodology and Findings

  • Endometrial tissues from different phases of the estrous cycle were exposed to varying concentrations of cortisol for 24 hours. The PGF secretion, as well as the expression of genes related to the AA cascade, were then analysed.
  • The study confirmed that GCR was present both in the cytoplasm and the nucleus of the luminal and glandular endometrium as well as in the stroma. The abundance of endometrial GCR protein was shown to increase during the late luteal phase of the estrous cycle.
  • The researchers found that as cortisol concentration increased, there was a corresponding decrease in PGF secretion, and in the expression of PLA2G2A and PLA2G4A, which are genes involved in the AA cascade, in endometrial tissues.
  • In addition to this, cortisol treatment also resulted in decreased PGF secretion from endometrial epithelial and stromal cells.
  • Moreover, cortisol was found to have affected the PLA2G2A, PLA2G4A, and PTGS2 transcripts in endometrial stromal cells.

Conclusions of the Research

  • The research study provides evidence that cortisol suppresses the production of PGF in the equine endometrium during the estrous cycle by influencing the AA cascade.
  • This conclusion adds to the understanding of the role played by cortisol, as an active form of glucocorticoids, in the reproductive process, particularly in relation to the equine endometrium which holds significant implications for equine reproduction.

Cite This Article

APA
Szóstek-Mioduchowska AZ, Shiotani H, Yamamoto Y, Sadowska A, Wójtowicz A, Kozai K, Hojo T, Kimura K, Skarzynski DJ, Okuda K. (2021). Effects of cortisol on prostaglandin F2α secretion and expression of genes involved in the arachidonic acid metabolic pathway in equine endometrium – In vitro study. Theriogenology, 173, 221-229. https://doi.org/10.1016/j.theriogenology.2021.08.009

Publication

ISSN: 1879-3231
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 173
Pages: 221-229
PII: S0093-691X(21)00271-5

Researcher Affiliations

Szóstek-Mioduchowska, Anna Z
  • Department of Reproductive Immunology and Pathology Institute of Animal Reproduction and Food Research Polish Academy of Sciences, Olsztyn, Poland. Electronic address: a.szostek-mioduchowska@pan.olsztyn.pl.
Shiotani, Haruki
  • Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Yamamoto, Yuki
  • Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Sadowska, Agnieszka
  • Department of Reproductive Immunology and Pathology Institute of Animal Reproduction and Food Research Polish Academy of Sciences, Olsztyn, Poland.
Wójtowicz, Anna
  • Department of Reproductive Immunology and Pathology Institute of Animal Reproduction and Food Research Polish Academy of Sciences, Olsztyn, Poland.
Kozai, Keisuke
  • Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Hojo, Takuo
  • Livestock and Grassland Research Division, Kyushu Okinawa Agricultural Research Center, National Agriculture and Food Research Organization (NARO), Kumamoto, Japan.
Kimura, Koji
  • Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Skarzynski, Dariusz J
  • Department of Reproductive Immunology and Pathology Institute of Animal Reproduction and Food Research Polish Academy of Sciences, Olsztyn, Poland.
Okuda, Kiyoshi
  • Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan; Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Japan.

MeSH Terms

  • Animals
  • Arachidonic Acid / metabolism
  • Arachidonic Acid / pharmacology
  • Dinoprost / metabolism
  • Dinoprost / pharmacology
  • Dinoprostone / metabolism
  • Endometrium / metabolism
  • Female
  • Horses
  • Hydrocortisone / metabolism
  • Metabolic Networks and Pathways

Conflict of Interest Statement

Declaration of competing interest The authors declare that there is no conflict of interest.

Citations

This article has been cited 2 times.
  1. Alpoim-Moreira J, Szóstek-Mioduchowska A, Słyszewska M, Rebordão MR, Skarzynski DJ, Ferreira-Dias G. 5-Aza-2'-Deoxycytidine (5-Aza-dC, Decitabine) Inhibits Collagen Type I and III Expression in TGF-β1-Treated Equine Endometrial Fibroblasts.. Animals (Basel) 2023 Mar 30;13(7).
    doi: 10.3390/ani13071212pubmed: 37048467google scholar: lookup
  2. 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