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Theriogenology2000; 52(7); 1181-1192; doi: 10.1016/S0093-691X(99)00210-1

Dynamics of prostaglandin secretion, intrauterine fluid and uterine clearance in reproductively normal mares and mares with delayed uterine clearance.

Abstract: Two experiments were performed to investigate relationships between oxytocin, prostaglandin release, uterine emptying and fluid accumulation in the uterus. In Experiment 1, the effect of oxytocin on the pattern of prostaglandin release during uterine clearance of radiocolloid was measured in 5 normal mares and 5 mares with delayed uterine clearance. Uterine clearance was measured during estrus by scintigraphy at 0, 60 and 120 min after colloid infusion. After the 120-min reading, 20 IU, i.v., oxytocin were given, and the amount of colloid cleared was measured at 135, 150 and 180 min. Plasma was obtained prior to and during scintigraphy at 5- and 15-min intervals to measure concentrations of 15-keto-13,14-dihydro-PGF2 alpha metabolite (PGFM) by RIA. In Experiment 2, plasma PGFM levels were compared after administration of oxytocin in 8 normal mares and 6 mares with delayed uterine clearance to determine if intrauterine fluid stimulated prostaglandin release. Mares received 2 treatments in a cross-over design. Treatment 1 consisted of 20 IU, i.v., oxytocin during estrus. Treatment 2 consisted of an infusion of 10 mL, i.u., saline 15 min prior to oxytocin administration. Treatments were performed 4 to 6 h apart. Blood was collected and PGFM was measured as in experiment 1. Data were analyzed by least squares analysis of variance. In Experiment 1, regression analysis of scintigraphy and PGFM profiles indicated that time response curves differed between groups (P < 0.01). At 120 min, normal mares retained 40.4 +/- 4.9% (mean +/- SEM) of the radiocolloid while mares with delayed clearance retained 88 +/- 5%. Fifteen minutes after oxytocin administration (135 min), all normal mares and 4 of 5 mares with delayed clearance retained only < 6% of the colloid. During the first 120 min, plasma PGFM concentrations did not differ between the 2 groups. After oxytocin was given, plasma PGFM concentrations increased in 4 of 5 mares with delayed uterine clearance (80 to 3,096 pg/mL) but not in normal mares (13 to 46 pg/mL). In Experiment 2, plasma PGFM concentrations did not rise in normal mares but rose in 3 of 6 mares with delayed clearance (135 to 483 pg/mL) independent of treatment or period. The results suggest that intrauterine clearance of radiocolloid after oxytocin administration appears to be independent of PGF2 alpha release in normal mares during estrus. The difference in prostaglandin release response after oxytocin administration between the 2 groups was unrelated to the presence of intrauterine fluid.
Publication Date: 2000-03-29 PubMed ID: 10735096DOI: 10.1016/S0093-691X(99)00210-1Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research investigated relationships between substances involved in the reproductive process of mares and how these might be different in mares with delayed uterine clearance. It suggests that delayed uterine clearance is not due to the presence of intrauterine fluid or prostaglandin releases.

Objective

The primary aim of this study was to understand the dynamics of oxytocin, prostaglandin release, and uterine clearance in normal mares and mares with delayed uterine clearance. Two experiments were carried out to investigate these relationships and their potential influences on uterine fluid accumulation.

Methodology

  • The first experiment involved a study on the impact of oxytocin on prostaglandin release during uterus clearance. This experiment involved 10 mares, half of which had normal uterine clearance, and the other half experienced delayed clearance.
  • The mares were infused with a radiocolloid and the uterine clearance was measured at various intervals. Blood plasma was obtained to measure various hormone concentrations.
  • Oxytocin was administered, and the amount of colloid cleared was measured again. Changes in plasma concentrations were also tracked.
  • The second experiment, involving a new set of 14 mares, was designed to understand the relationship between oxytocin administration and plasma PGFM levels in mares with and without delayed uterine clearance.
  • The mares received two treatments; one included oxytocin administration, and the other involved a saline infusion before administering oxytocin. Hormone levels post treatments were tracked as in the first experiment.

Results

  • In the first experiment, data analysis suggested that the time response curves differ between mares with normal uterine clearance and those with delayed clearance. After the administration of oxytocin, more radiocolloid was cleared from the uterus in both groups, but this was not tied to an increase in plasma PGFM concentrations in the normal mares.
  • In the second experiment, though plasma PGFM levels did rise in some mares with delayed clearance after oxytocin administration, this was not consistent and was again independent of the presence of intrauterine fluid.

Conclusion

This study’s findings indicate that in normal mares, the uterine clearance of radiocolloid post administration of oxytocin is not dependent on the release of PGF2 alpha. Both experiments also suggested that the different responsiveness to oxytocin between the two groups of mares is not due to the presence of intrauterine fluid.

Cite This Article

APA
Cadario ME, Thatcher WW, Klapstein E, Merrit AM, Archbald LF, Thatcher MJ, LeBlanc MM. (2000). Dynamics of prostaglandin secretion, intrauterine fluid and uterine clearance in reproductively normal mares and mares with delayed uterine clearance. Theriogenology, 52(7), 1181-1192. https://doi.org/10.1016/S0093-691X(99)00210-1

Publication

ISSN: 0093-691X
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 52
Issue: 7
Pages: 1181-1192

Researcher Affiliations

Cadario, M E
  • Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610, USA.
Thatcher, W W
    Klapstein, E
      Merrit, A M
        Archbald, L F
          Thatcher, M J
            LeBlanc, M M

              MeSH Terms

              • Animals
              • Cross-Over Studies
              • Dinoprost / analogs & derivatives
              • Dinoprost / blood
              • Dinoprost / metabolism
              • Estrus
              • Female
              • Horses
              • Inflammation
              • Least-Squares Analysis
              • Oxytocin / pharmacology
              • Prostaglandins / metabolism
              • Radioimmunoassay
              • Radionuclide Imaging
              • Reference Values
              • Regression Analysis
              • Streptococcus / physiology
              • Uterus / diagnostic imaging
              • Uterus / drug effects
              • Uterus / physiology

              Citations

              This article has been cited 4 times.
              1. 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
              2. Canisso IF, Segabinazzi LGTM, Fedorka CE. Persistent Breeding-Induced Endometritis in Mares - a Multifaceted Challenge: From Clinical Aspects to Immunopathogenesis and Pathobiology.. Int J Mol Sci 2020 Feb 20;21(4).
                doi: 10.3390/ijms21041432pubmed: 32093296google scholar: lookup
              3. Falomo ME, Ferroni L, Tocco I, Gardin C, Zavan B. Immunomodulatory Role of Adipose-Derived Stem Cells on Equine Endometriosis.. Biomed Res Int 2015;2015:141485.
                doi: 10.1155/2015/141485pubmed: 26180781google scholar: lookup
              4. Maischberger E, Irwin J, Carrington S, Duggan V. Equine post-breeding endometritis: A review.. Ir Vet J 2008 Mar 1;61(3):163-8.
                doi: 10.1186/2046-0481-61-3-163pubmed: 21851709google scholar: lookup