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American journal of veterinary research2001; 62(4); 526-530; doi: 10.2460/ajvr.2001.62.526

Microvascular development and growth of uterine tissue during the estrous cycle in mares.

Abstract: To document uterine growth and microvascular development in the endometrium of uteri with differing degrees of fibrosis as well as uterine growth throughout the estrous cycle of mares. Methods: 30 mares. Methods: Uterine tissue was obtained during the breeding season from a slaughter facility. Stage of estrous cycle of the mares was assessed on the basis of ovarian structures and plasma progesterone concentrations. Endometrium was characterized by use of light microscopy, and blood vessel walls were marked by histochemical techniques. Microvascular development was evaluated by a computerized image analysis system. Growth of uterine tissue was based on cellular content of DNA and RNA, RNA:DNA, and protein:DNA. Results: Significant differences in vascular density were not observed in the endometrium of uteri obtained from mares euthanatized during the follicular or luteal phase of the estrous cycle, regardless of whether endometrial classification of degree of fibrosis was considered. There was a 3-fold increase in amount of DNA and RNA of endometrial cells in the follicular phase when compared to myometrium. Hypertrophy of endometrial tissue during the luteal phase was reflected by a significant increase in cell protein content and protein:DNA. Conclusions: Endometrial growth of vascular tissues during the estrous cycle may be coordinated with development of nonvascular tissue. Estrogen and progesterone may play a role in regulation of uterine growth and angiogenesis.
Publication Date: 2001-05-01 PubMed ID: 11327459DOI: 10.2460/ajvr.2001.62.526Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The study explores the activity of uterine tissue growth and microvascular (small blood vessels) development during the various stages of the estrous (reproductive) cycle in mares (female horses). No significant differences were observed in the vascular density of the uterine tissue between the follicular and luteal phase, regardless of the degree of fibrosis present in the tissue. However, several variations in the cellular content of endometrial cells were observed, suggesting a relationship between the development of vascular and non-vascular tissues. It also indicates a potential role of hormones such as estrogen and progesterone in regulating these processes.

Methods

  • The researchers obtained uterine tissue from 30 mares during the breeding season from a slaughter facility.
  • The stage of the estrous cycle for each mare was determined by observing the ovarian structures and plasma progesterone concentrations.
  • They used light microscopy for characterizing the endometrium and histochemical techniques to mark the blood vessel walls.
  • A computerized image analysis system was used to evaluate microvascular development.
  • The growth of the uterine tissue was determined by analyzing the cellular content of DNA and RNA, and calculating the ratios of RNA:DNA and protein:DNA.

Results

  • They observed no significant differences in vascular density (number of blood vessels) in the uterine tissue collected from mares either in the follicular or luteal phase of the estrous cycle.
  • The classification of the degree of fibrosis (scarring or thickening of tissues due to excess fibrous connective tissue) in the endometrium did not affect these findings.
  • There was a threefold increase in the amount of both DNA and RNA in the endometrial cells during the follicular phase compared to the myometrium (muscular layer of the uterus).
  • The researchers detected hypertrophy (increase in the size of cells) of the endometrial tissue during the luteal phase, indicated by a significant increase in the cell protein content and the protein:DNA ratio.

Conclusions

  • The study suggests that the growth of vascular tissues in the endometrium during the estrous cycle is synchronized with the development of non-vascular tissue.
  • The results also indicate that hormones, specifically estrogen and progesterone, might have a role in regulating uterine growth and angiogenesis (formation of new blood vessels).

Cite This Article

APA
Ferreira-Dias GM, Serrão PM, Durão JF, Silva JR. (2001). Microvascular development and growth of uterine tissue during the estrous cycle in mares. Am J Vet Res, 62(4), 526-530. https://doi.org/10.2460/ajvr.2001.62.526

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 62
Issue: 4
Pages: 526-530

Researcher Affiliations

Ferreira-Dias, G M
  • Faculdade de Medicina Veterinária, Centro de Investigação Interdisciplinar em Sanidade Animal, Polo Universitário Alto da Ajuda, Lisbon, Portugal.
Serrão, P M
    Durão, J F
      Silva, J R

        MeSH Terms

        • Animals
        • DNA / analysis
        • Endometrium / blood supply
        • Endometrium / physiology
        • Estrus / physiology
        • Female
        • Fibrosis / pathology
        • Fibrosis / veterinary
        • Horses / physiology
        • Image Processing, Computer-Assisted
        • Microcirculation / physiology
        • Neovascularization, Physiologic / physiology
        • Progesterone / blood
        • Proteins / analysis
        • RNA / analysis

        Citations

        This article has been cited 2 times.
        1. Pinto-Bravo P, Rebordão MR, Amaral A, Fernandes C, Galvão A, Silva E, Pessa-Santos P, Alexandre-Pires G, Roberto da Costa RP, Skarzynski DJ, Ferreira-Dias G. Microvascularization and Expression of Fibroblast Growth Factor and Vascular Endothelial Growth Factor and Their Receptors in the Mare Oviduct. Animals (Basel) 2021 Apr 12;11(4).
          doi: 10.3390/ani11041099pubmed: 33921416google scholar: lookup
        2. Alexandre-Pires G, Mateus L, Martins C, Ferreira-Dias G. Seasonal Changes in Testes Vascularisation in the Domestic Cat (Felis domesticus): Evaluation of Microvasculature, Angiogenic Activity, and Endothelial Cell Expression. Anat Res Int 2012;2012:583798.
          doi: 10.1155/2012/583798pubmed: 22567311google scholar: lookup