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Anatomia, histologia, embryologia2026; 55(5); e70166; doi: 10.1111/ahe.70166

Histomorphometric and Histochemical Changes in the Mare Tuba Uterina During the Oestrous Cycle and Follicular Cyst Condition.

Abstract: This study evaluated histomorphometric and histochemical changes in the mare tuba uterina during different reproductive stages and under follicular cyst conditions. Forty nonpregnant mares were classified into follicular, luteal, post-ovulation and follicular cyst groups (n = 10/group). Histological evaluation of the isthmus, ampulla and infundibulum was performed using haematoxylin and eosin staining, while periodic acid-Schiff (PAS) staining was used to assess epithelial secretory activity. Morphometric parameters included number of primary mucosal folds, fold length, epithelial height and fold thickness. Descriptive observations indicated that the infundibulum possessed the most elaborate mucosal architecture, whereas the isthmus exhibited the simplest organization. Comparisons among reproductive stages were performed separately within each oviductal region. Across all oviductal regions, the follicular phase demonstrated the highest morphometric values, characterized by increased fold number, epithelial height and fold dimensions (p < 0.05). In contrast, most morphometric parameters decreased during the luteal and post-ovulation stages. For most variables, post-ovulation values remained higher than those observed during the luteal phase. The ampulla exhibited the strongest PAS reactivity during the luteal phase, with abundant apical PAS-positive granules indicating enhanced epithelial secretory activity, whereas moderate staining was observed during the follicular phase. Mares with follicular cysts showed the lowest morphometric values in all oviductal regions and weak, irregular PAS reactivity. These findings demonstrate that the mare tuba uterina undergoes pronounced cyclical remodelling influenced by ovarian status. Follicular cysts were associated with altered histological and secretory characteristics of the oviduct, which may compromise the physiological environment required for normal reproductive function.
Publication Date: 2026-08-15 PubMed ID: 42603111PubMed Central: PMC13476905DOI: 10.1111/ahe.70166Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study analyzed structural and chemical changes in the mare’s fallopian tube (tuba uterina) during the reproductive cycle and in the presence of follicular cysts.
  • It aimed to understand how tissue architecture and secretory activity vary with reproductive stages and ovarian cyst conditions, potentially affecting fertility.

Background and Objectives

  • The mare tuba uterina, analogous to the fallopian tube in humans, plays a critical role in gamete transport, fertilization, and maintaining an optimal environment for early embryo development.
  • Previous knowledge about how the mare’s oviduct changes during different reproductive phases or in pathological conditions like follicular cysts was limited.
  • This study’s goal was to evaluate both morphological (histomorphometric) changes and secretory activity (histochemical changes) of the mare tuba uterina during:
    • The follicular phase (before ovulation)
    • The luteal phase (after ovulation)
    • Post-ovulation phase
    • Follicular cyst condition

Materials and Methods

  • Forty nonpregnant mares were divided equally into four groups representing reproductive stages and the follicular cyst condition (10 mares per group).
  • Three regions of the mare’s oviduct were studied:
    • Isthmus (near uterus)
    • Ampulla (middle segment)
    • Infundibulum (near ovary)
  • Histological staining techniques used:
    • Haematoxylin and eosin staining — to analyze tissue architecture and conduct histomorphometric measurements.
    • Periodic acid-Schiff (PAS) staining — to detect epithelial secretory activity by visualizing carbohydrate-rich secretory granules.
  • Morphometric parameters quantified included:
    • Number of primary mucosal folds (which increase surface area)
    • Fold length
    • Epithelial height
    • Fold thickness

Key Findings

  • Mucosal Architecture:
    • Infundibulum showed the most complex and elaborate mucosal folds, indicating a highly folded surface.
    • Isthmus had the simplest mucosal organization, likely reflecting functional differences along the tube.
  • Reproductive Stage Changes:
    • Across all parts of the oviduct during the follicular phase:
      • Highest morphometric values were recorded, with increased fold number, epithelial height, and fold dimensions.
      • This suggests the oviduct is maximally prepared structurally to support gamete and embryo transport.
    • During luteal and post-ovulation phases:
      • Most morphometric parameters decreased, indicating tissue remodeling after ovulation.
      • Values post-ovulation remained somewhat higher than during the luteal phase, perhaps reflecting gradual recovery towards the next cycle.
  • Secretory Activity (PAS Staining):
    • Ampulla exhibited the strongest secretory activity during the luteal phase, with abundant apical PAS-positive granules in epithelial cells.
    • Moderate secretory staining was observed during the follicular phase.
    • This suggests that secretions are hormonally regulated and vary with ovarian cycle stages, likely influencing the microenvironment for fertilization and embryo support.
  • Follicular Cyst Condition Effects:
    • Mares with follicular cysts showed the lowest morphometric values across all regions.
    • Weak and irregular PAS reactivity indicated impaired or altered epithelial secretory function.
    • These changes may create a suboptimal environment for fertilization or early embryo development, potentially contributing to reproductive failure or subfertility associated with cystic conditions.

Conclusions and Implications

  • The mare tuba uterina undergoes marked cyclical remodeling in structure and secretory activity, driven by ovarian hormonal status throughout the estrous cycle.
  • This remodeling ensures optimal oviductal conditions tailored for different reproductive stages, supporting gamete transport, fertilization, and embryo viability.
  • The presence of follicular cysts disrupts normal histological architecture and secretory patterns, potentially compromising fertility by altering the physiological environment.
  • Understanding these changes can help in veterinary reproductive management and in developing treatments for reproductive disorders tied to follicular cysts.

Cite This Article

APA
Van Dung B, Anh NTL, Nam NH. (2026). Histomorphometric and Histochemical Changes in the Mare Tuba Uterina During the Oestrous Cycle and Follicular Cyst Condition. Anat Histol Embryol, 55(5), e70166. https://doi.org/10.1111/ahe.70166

Publication

ISSN: 1439-0264
NlmUniqueID: 7704218
Country: Germany
Language: English
Volume: 55
Issue: 5
Pages: e70166
PII: e70166

Researcher Affiliations

Van Dung, Bui
  • Department of Animal Surgery and Theriogenology, Faculty of Veterinary Medicine, Vietnam National University of Agriculture, Hanoi, Vietnam.
Anh, Nguyen Thi Lan
  • Department of Animal Surgery and Theriogenology, Faculty of Veterinary Medicine, Vietnam National University of Agriculture, Hanoi, Vietnam.
Nam, Nguyen Hoai
  • Department of Animal Surgery and Theriogenology, Faculty of Veterinary Medicine, Vietnam National University of Agriculture, Hanoi, Vietnam.

MeSH Terms

  • Animals
  • Female
  • Horses / physiology
  • Horses / anatomy & histology
  • Estrous Cycle / physiology
  • Follicular Cyst / veterinary
  • Follicular Cyst / pathology
  • Fallopian Tubes / anatomy & histology
  • Fallopian Tubes / physiology
  • Uterus / anatomy & histology
  • Periodic Acid-Schiff Reaction / veterinary

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 42 references
  1. Abiaezute CN, Nwaogu IC, Igwebuike UM. Evaluation of the Morphological Features of the Uterine Tubes During Postnatal Development in West African Dwarf Goats (). Veterinary Research Forum 8, no. 1: 1–6.
    pmc: PMC5413304pubmed: 28473890
  2. Aguilar JJ, Cuervo-Arango J, Mouguelar H, Losinno L. Histological Characteristics of the Equine Oviductal Mucosa at Different Reproductive Stages. Journal of Equine Veterinary Science 32, no. 2: 99–105.
  3. Almeida J, Ball BA, Conley AJ. Biological and Clinical Significance of Anti‐Müllerian Hormone Determination in Blood Serum of the Mare. Theriogenology 76, no. 8: 1393–1403.
  4. Aurich C, Kaps M. Suppression of Reproductive Behaviour and Gonadal Function in Female Horses‐An Update. Reproduction in Domestic Animals 57, no. 4: 4–12.
    doi: 10.1111/rda.14129pmc: PMC9790428pubmed: 35467049google scholar: lookup
  5. Ball BA, Almeida J, Conley AJ. Determination of Serum Anti‐Müllerian Hormone Concentrations for the Diagnosis of Granulosa‐Cell Tumours in Mares. Equine Veterinary Journal 45, no. 2: 199–203.
  6. Bashir ST, Gastal MO, Tazawa SP. The Mare as a Model for Luteinized Unruptured Follicle Syndrome: Intrafollicular Endocrine Milieu. Reproduction 151, no. 3: 271–283.
    doi: 10.1530/REP-15-0457pubmed: 26647418google scholar: lookup
  7. Bergfelt DR. Anatomy and Physiology of the Mare. In Equine Breeding Management and Artificial Insemination, 2nd ed. Elsevier.
  8. Crabtree JR. A Review of Oestrus Suppression Techniques in Mares. Equine Veterinary Education 34, no. 3: 141–151.
    doi: 10.1111/eve.13405google scholar: lookup
  9. Cuervo-Arango J, Newcombe JR. Ultrasound Confirmation of Ovulation in Mares: A Normal Corpus Luteum or a Haemorrhagic Anovulatory Follicle?. Reproduction in Domestic Animals 48, no. 1: 105–111.
  10. Desantis S, Zizza S, Accogli G, Acone F, Rossi R, Resta L. Morphometric and Ultrastructural Features of the Mare Oviduct Epithelium During Oestrus. Theriogenology 75, no. 4: 671–678.
  11. Duszewska A, Compa A, Zelechowska M. Comparison of the Morphology of Various Regions of the Cattle Oviduct in Four Phases of the Ovarian Cycle. Reproduction, Fertility, and Development 24, no. 1: 140–145.
    doi: 10.1071/RDv24n1Ab56google scholar: lookup
  12. El-Maaty AMA, Abdelnaby EA. Follicular Blood Flow, Antrum Growth and Angiogenic Mediators in Mares From Ovulation to Deviation. Animal Reproduction 14, no. 4: 1043–1056.
    doi: 10.21451/1984-3143-AR848google scholar: lookup
  13. Ghersevich S, Massa E, Zumoffen C. Oviductal Secretion and Gamete Interaction. Reproduction 149, no. 1: R1–R14.
    doi: 10.1530/REP-14-0145pubmed: 25190504google scholar: lookup
  14. González N, Varela A, de Blas N, Gil L. Changes in the Mare Oviduct Across Different Seasons Throughout the Year. Veterinary Medicine and Science 12, no. 2: e70753.
    doi: 10.1002/vms3.70753pmc: PMC13054841pubmed: 41830181google scholar: lookup
  15. Goudet G. Fertilisation in the Horse and Paracrine Signalling in the Oviduct. Reproduction, Fertility and Development 23, no. 8: 941–951.
    doi: 10.1071/RD10285pubmed: 22127000google scholar: lookup
  16. Huggins L, Norris J, Conley A, Dini P. Abnormal Mare Behaviour Is Rarely Associated With Changes in Hormonal Markers of Granulosa Cell Tumours: A Retrospective Study. Equine Veterinary Journal 56, no. 4: 759–767.
    doi: 10.1111/evj.13967pubmed: 37344926google scholar: lookup
  17. Hunter RH. The Fallopian Tubes in Domestic Mammals: How Vital Is Their Physiological Activity. Reproduction, Nutrition, Development 45, no. 3: 281–290.
    doi: 10.1051/rnd:2005020pubmed: 15982454google scholar: lookup
  18. Kikuchi K, Kozai K, Hojo T. Evaluating the Electrical Impedance and Mucus‐Related Gene Expression of Uterine Endometrial Tissues in Mares. Journal of Reproduction and Development 64, no. 2: 193–197.
    doi: 10.1262/jrd.2017-128pmc: PMC5902908pubmed: 29311525google scholar: lookup
  19. Leemans B, Gadella BM, Stout TAE. Why Does Not Conventional IVF Work in the Horse? The Equine Oviduct as a Microenvironment for Capacitation/Fertilization. Reproduction 152, no. 6: R233–R245.
    doi: 10.1530/REP-16-0420pubmed: 27651517google scholar: lookup
  20. Lefranc AC, Allen WR. Incidence and Morphology of Anovulatory Haemorrhagic Follicles in the Mare. Pferdeheilkunde Equine Medicine 19, no. 6: 611–612.
  21. Mahé C, Lavigne R, Com E. Spatiotemporal Profiling of the Bovine Oviduct Fluid Proteome Around the Time of Ovulation. Scientific Reports 12: 4135.
    doi: 10.1038/s41598-022-07929-3pmc: PMC8907256pubmed: 35264682google scholar: lookup
  22. Małysz‐Cymborska I, Andronowska A. Expression of the Vascular Endothelial Growth Factor Receptor System in Porcine Oviducts After Induction of Ovulation and Superovulation. Domestic Animal Endocrinology 49: 86–95.
  23. Mokhtar DM. Microscopic and Histochemical Characterization of the Bovine Uterine Tube During the Follicular and Luteal Phases of Estrous Cycle. Journal of Microscopy and Ultrastructure 3, no. 1: 44–52.
    doi: 10.1016/j.jmau.2014.09.002pmc: PMC6014219pubmed: 30023181google scholar: lookup
  24. Mouguelar H, Díaz T, Borghi D. Morphometric Study of the Mare Oviductal Mucosa at Different Reproductive Stages. Anatomical Record 298, no. 11: 1950–1959.
    doi: 10.1002/ar.23193pubmed: 26136388google scholar: lookup
  25. Nelis HM, Goossens K, Leemans B, Peelman L, Van Soom A. Steroid‐Regulated mRNA Expression in Oviduct Epithelial Cells in the Mare. Reproduction, Fertility, and Development 25: 258.
    doi: 10.1071/RDv25n1Ab220google scholar: lookup
  26. Nelissen S, Miller AD. Comparison of Anti‐Müllerian Hormone and Inhibin Immunolabeling in Canine and Equine Granulosa Cell Tumors. Journal of Veterinary Diagnostic Investigation 34, no. 6: 1027–1031.
    doi: 10.1177/10406387221124589pmc: PMC9597338pubmed: 36113168google scholar: lookup
  27. Ortega HH, Díaz PU, Salvetti NR. Follicular Cysts: A Single Sign and Different Diseases. A View From Comparative Medicine. Current Pharmaceutical Design 22, no. 36: 5634–5645.
  28. Panzani D, Di Vita M, Lainé A-L. Corpus Luteum Vascularization and Progesterone Production in Autumn and Winter Cycles of the Mare: Relationship Between Ultrasonographic Characteristics of Corpora Lutea and Plasma Progesterone Concentration in the Last Cycles Before Anestrus. Journal of Equine Veterinary Science 56: 35–39.
  29. Pérez-Cerezales S, Ramos-Ibeas P, Acuña OS. The Oviduct: From Sperm Selection to the Epigenetic Landscape of the Embryo. Biology of Reproduction 98, no. 3: 262–276.
    doi: 10.1093/biolre/iox173pubmed: 29228115google scholar: lookup
  30. Pinto-Bravo P, Galvão A, Rebordão MR. Ovarian Steroids, Oxytocin, and Tumor Necrosis Factor Modulate Equine Oviduct Function. Domestic Animal Endocrinology 61: 84–99.
  31. Saint‐Dizier M, Schoen J, Chen S, Banliat C, Mermillod P. Composing the Early Embryonic Microenvironment: Physiology and Regulation of Oviductal Secretions. International Journal of Molecular Sciences 21, no. 1: 223.
    doi: 10.3390/ijms21010223pmc: PMC6982147pubmed: 31905654google scholar: lookup
  32. Schätz G, Schneiter M, Rička J. Ciliary Beating Plane and Wave Propagation in the Bovine Oviduct. Cells, Tissues, Organs 198, no. 6: 457–469.
    doi: 10.1159/000360155pubmed: 24713584google scholar: lookup
  33. Scully D, Reese S, Kölle S. Cystic Ovary Disease (COD) Alters Structure and Function of the Bovine Oviduct. Molecular Reproduction and Development 91, no. 1: e23725.
    doi: 10.1002/mrd.23725pubmed: 38282319google scholar: lookup
  34. Stefańczyk‐Krzymowska S, Krzymowski T. Local Adjustment of Blood and Lymph Circulation in the Hormonal Regulation of Reproduction in Female Pigs‐Facts, Conclusions and Suggestions for Future Research. Reproductive Biology 2, no. 2: 115–132.
    pubmed: 14666153
  35. Stefańczyk‐Krzymowska S, Krzymowski T, Wasowska B, Chlopek J. Retrograde Transfer of Ovarian Steroid Hormones to the Ovary in the Porcine Periovarian Vascular Complex. Experimental Physiology 87, no. 3: 361–371.
    doi: 10.1113/eph8702338pubmed: 12089604google scholar: lookup
  36. Stout T A E, Colenbrander B. Suppressing Reproductive Activity in Horses Using GnRH Vaccines, Antagonists or Agonists. Animal Reproduction Science 82–83: 633–643.
  37. Tsogtgerel M, Tagami M, Watanabe K. Case Report: The Case of a 17 kg Ovarian Granulosa Cell Tumor in a Breton Draft Mare. Journal of Equine Science 32, no. 2: 67–72.
    doi: 10.1294/jes.32.67pmc: PMC8240524pubmed: 34220274google scholar: lookup
  38. Van Dung B, Nam N H. Uterine Tube Changes in Cattle: A Morphometric Study Across Estrous Phases and Follicular Cysts. Iranian Journal of Veterinary Medicine In Press.
  39. Weber J A, Freeman D A, Vanderwall D K, Woods G L. Prostaglandin E2 Hastens Oviductal Transport of Equine Embryos. Biology of Reproduction 45, no. 4: 544–546.
    doi: 10.1095/biolreprod45.4.544pubmed: 1751628google scholar: lookup
  40. Witte T S, Wolf N, Walter I, Hahn J A, Zerbe H. Pathohistological Findings in Bilateral Removed Ovaries of Mares With Behavioral Problems. Journal of Equine Veterinary Science 125: 104754.
  41. Wolf N, Hahn J A, Walter I, Zablotski Y, Zerbe H, Witte T S. Pathohistological Findings After Bilateral Ovariectomy in Mares With Behavioral Problems. Animals 14, no. 19: 2899.
    doi: 10.3390/ani14192899pmc: PMC11475726pubmed: 39409848google scholar: lookup
  42. Yaniz J L, Lopez‐Gatius F, Hunter R H. Scanning Electron Microscopic Study of the Functional Anatomy of the Porcine Oviductal Mucosa. Anatomia, Histologia, Embryologia 35, no. 1: 28–34.

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