Analyze Diet
Animals : an open access journal from MDPI2022; 12(21); 2966; doi: 10.3390/ani12212966

Equine Stomach Development in the Fetal Period: An Anatomical, Topographical, and Morphometric Study.

Abstract: Studies of equine stomach prenatal development are very rare, and descriptions usually focus on the processes taking place in the embryonic period. Only general information about gastric organogenesis in the fetal period is available in embryology textbooks on domestic mammals. The material for our study included twenty half-breed horse fetuses divided into three age groups on the basis of known fetal age (verified using the CRL method). Our study consists of the topographical, morphological, and morphometrical description of stomach development between the 4th and 11th months of gestation. Even though the skeletotopy, syntopy, and holotopy of the stomach in the fetal period seems to be relatively unchanged, the organ shape and the proportions between its anatomical parts differed in fetuses from the three age groups. The achieved results were statistically elaborated to estimate the dynamics of the stomach shape. This can be described as changing from medium-wide to wide and from slightly bent to sharply bent. A nonlinear correlation of all metric values with CRL in all age groups was observed. A positive allometric growth rate of different intensity was seen in all metric parameters. All the values increased as the fetal period progressed. Only the parietal surface growth rate gradually changed from strongly positive allometric in the first age group to strongly negative allometric in the third age group. A difference between the non-glandular and glandular mucosa of the stomach was visible in the first group. Development of a well-distinguishable plicated edge margin began in the second age group together with gastric pits and gastric areas. The third age group showed a well-developed gastric groove and angular incisura.
Publication Date: 2022-10-28 PubMed ID: 36359095PubMed Central: PMC9658733DOI: 10.3390/ani12212966Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article is a detailed study on the development of the stomach in horse fetuses from the 4th to the 11th month of gestation looking at topographical, morphological, and morphometrical aspects.

Objective of the Research

  • This research aims to shed light on the anatomical, topographical, and morphometric development of the equine stomach during the fetal period, a topic that has been rarely studied in depth. The desire is to fill these knowledge gaps and contribute new, robust data to the understanding of equine fetal development.

Methodology

  • The researchers utilized twenty half-breed horse fetuses as the subjects of their study. These fetuses were divided into three age groups based on their known fetal age, established and verified with the Crown Rump Length (CRL) method.
  • The research specifically examined changes to the stomach’s topography, morphology, and morphometry between the 4th and 11th months of gestation.

Key Findings

  • The research discovered that while the position (skeletotopy, syntopy, and holotopy) of the stomach doesn’t change significantly during the fetal period, the organ’s shape and proportions of its anatomical parts are altered across the three age groups.
  • The shape of the stomach specifically transitions from being medium-wide to broad, and from slightly curved to sharply bent as gestation progresses.
  • All metric values associated with the stomach correlated nonlinearly with CRL across all age groups, indicating a consistently positive but varying growth rate throughout the fetal period.
  • Peculiarly, the growth rate of the stomach’s parietal surface was found to shift from strongly positive allometric in the first age group to strongly negative allometric in the third age group.
  • The development of the non-glandular and glandular mucosa in the stomach was discernible from the first group.
  • Noticeable development of a plicated edge margin along with gastric pits and areas was seen in the second age group, while the third group exhibited a well-developed gastric groove and angular incisura.

Conclusion

  • This study provides valuable insights into the development of the equine stomach during the fetal period. It offers a deeper understanding of the anatomical and topographical transformations the stomach undergoes during gestation, revealing key changes and growth patterns at different stages.

Cite This Article

APA
Poradowski D, Chrószcz A. (2022). Equine Stomach Development in the Fetal Period: An Anatomical, Topographical, and Morphometric Study. Animals (Basel), 12(21), 2966. https://doi.org/10.3390/ani12212966

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 12
Issue: 21
PII: 2966

Researcher Affiliations

Poradowski, Dominik
  • Department of Biostructure and Animal Physiology, Division of Animal Anatomy, Faculty of Veterinary Medicine, Wroclaw University of Environmental and Life Sciences, Kożuchowska 1, 51-631 Wrocław, Poland.
Chrószcz, Aleksander
  • Department of Biostructure and Animal Physiology, Division of Animal Anatomy, Faculty of Veterinary Medicine, Wroclaw University of Environmental and Life Sciences, Kożuchowska 1, 51-631 Wrocław, Poland.

Conflict of Interest Statement

Neither of the authors has any financial or personal relationships that could inappropriately influence or bias the content of the paper.

References

This article includes 40 references
  1. Bucca S, Fogarty U, Collins A, Small V. Assessment of feto-placental well-being in the mare from mid-gestation to term: transrectal and transabdominal ultrasonographic features.. Theriogenology 2005 Aug;64(3):542-57.
  2. Murase H, Endo Y, Tsuchiya T, Kotoyori Y, Shikichi M, Ito K, Sato F, Nambo Y. Ultrasonographic evaluation of equine fetal growth throughout gestation in normal mares using a convex transducer.. J Vet Med Sci 2014 Jul;76(7):947-53.
    doi: 10.1292/jvms.13-0259pmc: PMC4143655pubmed: 24662520google scholar: lookup
  3. Agnew ME, Slack J, Stefanovski D, Linton JK, Sertich PL. Sonographic appearance of the late gestation equine fetal intestine.. Theriogenology 2019 Oct 15;138:121-126.
  4. Lanci A, Castagnetti C, Ranciati S, Sergio C, Mariella J. A regression model including fetal orbit measurements to predict parturition in Standardbred mares with normal pregnancy.. Theriogenology 2019 Mar 1;126:153-158.
  5. Bucca S, De Oliveira IRS, Cunanan JC, Vinardell T, Troedsson MHT. Doppler indices of the equine fetal carotid artery throughout gestation.. Theriogenology 2020 Oct 15;156:196-204.
  6. Schnorr B, Kressin M. Embriologie der Haustiere. 6th ed. Enke Verlag; Stuttgart, Germany: 2011.
  7. Rüsse I, Sinowatz F. Lehrbuch der Embriologie der Haustiere. Verlag Paul Parey; Berlin, Germany: Hamburg, Germany: 1991.
  8. Bielańska-Osuchowska Z. Zarys Organogenezy. 1st ed. PWN; Warszawa, Poland: 2004.
  9. Franciolli AL, Cordeiro BM, da Fonseca ET, Rodrigues MN, Sarmento CA, Ambrosio CE, de Carvalho AF, Miglino MA, Silva LA. Characteristics of the equine embryo and fetus from days 15 to 107 of pregnancy.. Theriogenology 2011 Sep 15;76(5):819-32.
  10. Cai WQ, Gabella G. Structure and innervation of the musculature at the gastroduodenal junction of the guinea-pig.. J Anat 1984 Aug;139 ( Pt 1)(Pt 1):93-104.
    pmc: PMC1164449pubmed: 6469859
  11. Karam SM, Leblond CP. Dynamics of epithelial cells in the corpus of the mouse stomach. I. Identification of proliferative cell types and pinpointing of the stem cell.. Anat Rec 1993 Jun;236(2):259-79.
    doi: 10.1002/ar.1092360202pubmed: 8338232google scholar: lookup
  12. Karam SM, Leblond CP. Dynamics of epithelial cells in the corpus of the mouse stomach. II. Outward migration of pit cells.. Anat Rec 1993 Jun;236(2):280-96.
    doi: 10.1002/ar.1092360203pubmed: 8338233google scholar: lookup
  13. Karam SM, Leblond CP. Dynamics of epithelial cells in the corpus of the mouse stomach. III. Inward migration of neck cells followed by progressive transformation into zymogenic cells.. Anat Rec 1993 Jun;236(2):297-313.
    doi: 10.1002/ar.1092360204pubmed: 8338234google scholar: lookup
  14. Karam SM. Dynamics of epithelial cells in the corpus of the mouse stomach. IV. Bidirectional migration of parietal cells ending in their gradual degeneration and loss.. Anat Rec 1993 Jun;236(2):314-32.
    doi: 10.1002/ar.1092360205pubmed: 8338235google scholar: lookup
  15. Karam SM, Leblond CP. Dynamics of epithelial cells in the corpus of the mouse stomach. V. Behavior of entero-endocrine and caveolated cells: general conclusions on cell kinetics in the oxyntic epithelium.. Anat Rec 1993 Jun;236(2):333-40.
    doi: 10.1002/ar.1092360206pubmed: 8338236google scholar: lookup
  16. Karam S, Leblond CP. Origin and migratory pathways of the eleven epithelial cell types present in the body of the mouse stomach.. Microsc Res Tech 1995 Jun 15;31(3):193-214.
    doi: 10.1002/jemt.1070310304pubmed: 7670159google scholar: lookup
  17. Kablar B. Structural study on the appearance of innervation in the stomach of mouse and rat embryos.. Tissue Cell 1995 Jun;27(3):309-15.
    doi: 10.1016/S0040-8166(95)80051-4pubmed: 7645008google scholar: lookup
  18. Asar M, Bayram Z, Korgun ET, Tertemiz F, Akkoyunlu G, Demir R. Immunocytochemical detection of synaptophysin in enteric neurones during prenatal development in the rat stomach.. Anat Histol Embryol 2004 Jun;33(3):135-40.
  19. Çetin A, Eşrefoğlu M. Prenatal and Postnatal Development of the Stomach in Wistar Albino Rats. J. Turgut Ozal Med. Cent. 2014;21:4–11.
  20. Steele MA, Penner GB, Chaucheyras-Durand F, Guan LL. Development and physiology of the rumen and the lower gut: Targets for improving gut health.. J Dairy Sci 2016 Jun;99(6):4955-4966.
    doi: 10.3168/jds.2015-10351pubmed: 26971143google scholar: lookup
  21. Green WW, Winters LM. Prenatal Development of the Sheep. University of Minnesota Agricultural Experiment Station; St. Paul, MN, USA: 1945. pp. 3–36. Technical Bulletin 169.
  22. Michel G, Flechsig G. [On the histogenesis of antestomach compartments and of abomasum in cattle with special reference to the development of mucous membrane structures].. Anat Anz 1969;124(4):403-18.
    pubmed: 4896626
  23. Georgieva R, Gerov K. The morphological and functional differentiation of the alimentary canal of the pig during ontogeny. I. Development and differentiation of the fundic portion of the stomach.. Anat Anz 1975;137(1-2):12-15.
    pubmed: 1163804
  24. Liebich HG, Scharrer E. [Developmental changes in the structure and function of the ruminal epithelium. 2. Morphological differentiation of the epithelial barrier in lambs during the first weeks of life].. Anat Histol Embryol 1984 Mar;13(1):25-41.
  25. Chrószcz A. The innervation and arterial blood supply of pig’s stomach in the fetal period. EJPAU 2008;11:3.
  26. Chrószcz A. The morphometric and topographic study of pig’s stomach development between the 35th and 114th day of gestation. EJPAU 2008;11:4.
  27. Chrószcz A. Morphology, development and histometry of swine gastric wall in the fetal period. EJPAU 2008;11:4.
  28. Rodrigues MN, Carvalho RC, Franciolli AL, Rodrigues RF, Rigoglio NN, Jacob JC, Gastal EL, Miglino MA. Prenatal development of the digestive system in the horse.. Anat Rec (Hoboken) 2014 Jul;297(7):1218-27.
    doi: 10.1002/ar.22929pubmed: 24778084google scholar: lookup
  29. Marrable AW. The Embryonic Pig a Chronological Account. 1st ed. Pitman Medical; London, UK: 1971.
  30. Nickel R, Schummer A, Seiferle E. Lehrbuch der Anatomie der Haustiere. 1st ed. Parey Verlag; Stuttgart, Germany: 2004.
  31. Bergin WC. Developmental Horizons and Measurement Useful for Age Determination of Equine Embryos and Fetuses. Master’s Thesis. Kansas State Unversity; Manhattan, KS, USA: 1969.
  32. Platt H. Growth and maturity in the equine fetus.. J R Soc Med 1978 Sep;71(9):658-61.
    doi: 10.1177/014107687807100906pmc: PMC1436262pubmed: 712744google scholar: lookup
  33. Bożiłow W, Sawicki K. Metody Badań Zmienności Cech Anatomicznych Człowieka Podczas Rozwoju Prenatalnego i Okołoporodowego. 1st ed. Akademia Medyczna; Wrocław, Poland: 1980.
  34. Stelmasiak M, Osemlak J, Siwek R. The shape and measurements of the stomach in Cercopithecus aethiops.. Folia Morphol (Warsz) 1981;39(3):233-43.
    pubmed: 6973512
  35. Biedermann F. Metrische Untersuchungen an Pferdemagen. Doctoral Thesis. Leipzig; Germany: 1921.
  36. International Committee on Veterinary Histological Nomenclature. Nomina Histologica Veterinaria (NHV). World Association of Veterinary Anatomists; Ghent, Belgium: 2017.
  37. International Committee on Veterinary Histological Nomenclature. Nomina Anatomica Veterinaria (NAV). 6th ed. World Association of Veterinary Anatomists; Ghent, Belgium: 2017.
  38. International Committee on Veterinary Histological Nomenclature. Nomina Embryologica Veterinaria (NEV). 2nd ed. World Association of Veterinary Anatomists; Ghent, Belgium: 2006.
  39. Klećkowska-Nawrot J, Dziegiel P. Morphology of lacrimal gland in pig fetuses.. Anat Histol Embryol 2008 Feb;37(1):74-7.
  40. Pospieszny N. Morfologia pni błędnych owcy w okresie płodowym. Zesz. Nauk. AR Wroc. S. Wet. 2000;381:71–77.

Citations

This article has been cited 2 times.
  1. Poradowski D, Chrószcz A. Equine Stomach Development in the Foetal Period of Prenatal Life-An Immunohistochemical Study. Animals (Basel) 2022 Dec 31;13(1).
    doi: 10.3390/ani13010161pubmed: 36611768google scholar: lookup
  2. Poradowski D, Chrószcz A. Equine Stomach Development in the Foetal Period of Prenatal Life-A Histological and Histometric Study. Animals (Basel) 2022 Nov 6;12(21).
    doi: 10.3390/ani12213047pubmed: 36359171google scholar: lookup