Analyze Diet
European journal of histochemistry : EJH2013; 57(2); e18; doi: 10.4081/ejh.2013.e18

Immunolocalization of succinate dehydrogenase in the esophagus epithelium of domesticated mammals.

Abstract: Using immunohistochemistry and transmission electron microscopy (TEM), the esophagus epithelia of seven domesticated mammals (horse, cattle, goat, pig, dog, laboratory rat, cat) of three nutrition groups (herbivorous, omnivorous, carnivorous) were studied to get first information about energy generation, as demonstrated by succinate dehydrogenase (SDH) activities. Distinct reaction intensities could be observed in all esophageal cell layers of the different species studied reflecting moderate to strong metabolic activities. The generally strong staining in the stratum basale indicated that new cells are continuously produced. The latter feature was confirmed by a thick, and in the horse generally highly active stratum spinosum. Only in the pig, reaction intensity variations occurred, obviously related to differences in physical feed quality or restricted feed allocation. The immunohistochemical results were corroborated by the presence of intact mitochondria in the esophageal cells of all species and nutrition types studied, except for the horse. Possible relationships between SDH reaction intensities and feed structure, mass or consistency are discussed.
Publication Date: 2013-05-10 PubMed ID: 23807297PubMed Central: PMC3794344DOI: 10.4081/ejh.2013.e18Google 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
  • Research Support
  • Non-U.S. Gov't

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 paper studies the activities of succinate dehydrogenase (SDH), an enzyme involved in energy generation, in the esophagus epithelia of several domesticated mammals. Using immunohistochemical and electron microscopy techniques, the research showed differences in SDH activity that may be related to the mammal’s diet and physical feed quality.

Study Methods

  • The researchers used immunohistochemistry and transmission electron microscopy (TEM) as their primary methods for studying the epithelial layers of the esophagus in seven types of domesticated animals: horses, cows, goats, pigs, dogs, rats, and cats.
  • The animals selected for study belong to three nutrition groups: herbivores (feeding mostly on plants), omnivores (having a diet of both plants and meat), and carnivores (feeding predominantly on meat).

Findings

  • The scientists were able to observe varying reaction intensities to the SDH activity across all the studied species, indicating a range of moderate to high metabolic activities. These activities could be related to the animals’ feed quality and diet type.
  • A strong reaction was generally found in the stratum basale, the deepest layer of the esophagus epithelium, suggesting the continuous production of new cells. The thick and typically highly active stratum spinosum in horses further confirmed this observation.
  • In pigs, however, variations in SDH activity were observed, possibly related to the quality of their feed or restricted feed allocation.

Mitochondrial Presence

  • The research team’s results were substantiated by observing the presence of intact mitochondria in the esophageal cells of all studied animals, with the sole exception being horses. The absence of healthy mitochondria in horses’ esophagus cells might need further evaluation.

Implications and Conclusion

  • The study discusses the potential relationships between SDH activity levels in the cells of the esophagus, and the structure, mass or consistency of the animals’ feed.
    This could provide valuable insights for dietary planning and nutritional management in domestic animals, particularly those bred for agriculture or livestock purposes.

Cite This Article

APA
Meyer W, Kacza J, Hornickel IN, Schoennagel B. (2013). Immunolocalization of succinate dehydrogenase in the esophagus epithelium of domesticated mammals. Eur J Histochem, 57(2), e18. https://doi.org/10.4081/ejh.2013.e18

Publication

ISSN: 2038-8306
NlmUniqueID: 9207930
Country: Italy
Language: English
Volume: 57
Issue: 2
Pages: e18
PII: e18

Researcher Affiliations

Meyer, W
  • Institute for Anatomy, University of Veterinary Medicine Hannover Foundation, 30173 Hannover, Germany. wilfried.meyer@tiho-hannover.de
Kacza, J
    Hornickel, I N
      Schoennagel, B

        MeSH Terms

        • Animals
        • Cats
        • Cattle
        • Diet / veterinary
        • Dogs
        • Epithelium / enzymology
        • Esophagus / enzymology
        • Feeding Behavior / physiology
        • Female
        • Goats
        • Horses
        • Immunohistochemistry
        • Male
        • Microscopy, Electron, Transmission
        • Rats
        • Succinate Dehydrogenase / metabolism
        • Swine

        References

        This article includes 27 references
        1. Meyer W, Kacza J, Schnapper A, Verspohl J, Hornickel I, Seeger J. A first report on the microbial colonisation of the equine oesophagus.. Ann Anat 2010 Feb 20;192(1):42-51.
          pubmed: 19942420doi: 10.1016/j.aanat.2009.10.004google scholar: lookup
        2. Nina Hornickel I, Kacza J, Schnapper A, Beyerbach M, Schoennagel B, Seeger J, Meyer W. Demonstration of substances of innate immunity in the esophageal epithelium of domesticated mammals: Part II--Defence mechanisms, including species comparison.. Acta Histochem 2011 Feb;113(2):175-88.
          pubmed: 20022082doi: 10.1016/j.acthis.2009.09.008google scholar: lookup
        3. Rutter J, Winge DR, Schiffman JD. Succinate dehydrogenase - Assembly, regulation and role in human disease.. Mitochondrion 2010 Jun;10(4):393-401.
          pmc: PMC2874626pubmed: 20226277doi: 10.1016/j.mito.2010.03.001google scholar: lookup
        4. Rich PR, Maréchal A. The mitochondrial respiratory chain.. Essays Biochem 2010;47:1-23.
          pubmed: 20533897doi: 10.1042/bse0470001google scholar: lookup
        5. Parsons MJ, Green DR. Mitochondria in cell death.. Essays Biochem 2010;47:99-114.
          pubmed: 20533903doi: 10.1042/bse0470099google scholar: lookup
        6. Reimer L. Electron spectroscopic imaging. In: Reimer L.(ed.)Energy Filtering-Transmission Electron Microscopy. Springer, 1995, pp. 347-93.
        7. Sillero-Zubiri S. Family Canidae. In: Wilson D.E., Mittermeier R.A.(eds.)Handbook of the mammals of the world, vol. 1, Carnivores. Lynx Edition, Barcelona, Spain, 2009, pp. 352-446.
        8. Schoennagel B. Vergleichende Untersuchungen zur Struktur und Funktion des Oesophagus-Epithels bei Vertebraten in Bezug zur Ernaehrun gsweise, unter besonderer Beruecksichtigung der Haussaeuge-tiere. Ph.D. Thesis, Univ Vet Med Hannover, Germany, 2005.
        9. Nina Hornickel I, Kacza J, Schnapper A, Beyerbach M, Schoennagel B, Seeger J, Meyer W. Demonstration of substances of innate immunity in the esophageal epithelium of domesticated mammals. Part I--Methods and evaluation of comparative fixation.. Acta Histochem 2011 Feb;113(2):163-74.
          pubmed: 19850328doi: 10.1016/j.acthis.2009.09.009google scholar: lookup
        10. Boeck P. Romeis Mikroskopische Technik. 17th ed., Urban und Schwarzenberg, Muenchen, Germany, 1989.
        11. Lillie RD, Fullmer HM. Histopathologic technic and practical histochemistry. McGraw-Hill, New York, USA, 1976.
        12. Pearse AGE. Histochemistry, Theoretical and Applied. 4th. ed vol. 2: Analytical technology; Churchill Livingstone, 1985.
        13. Karnovsky MJ. A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron microscopy. J Cell Biol 1965;27: 137A-8A.
        14. Millonig G. Advantages of a phosphate buffer for OsO4 solutions in fixation. J Appl Phys 1961;32:1637.
        15. LUFT JH. Improvements in epoxy resin embedding methods.. J Biophys Biochem Cytol 1961 Feb;9(2):409-14.
          pmc: PMC2224998pubmed: 13764136doi: 10.1083/jcb.9.2.409google scholar: lookup
        16. STEMPAK JG, WARD RT. AN IMPROVED STAINING METHOD FOR ELECTRON MICROSCOPY.. J Cell Biol 1964 Sep;22(3):697-701.
          pmc: PMC2106477pubmed: 14206430doi: 10.1083/jcb.22.3.697google scholar: lookup
        17. REYNOLDS ES. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.. J Cell Biol 1963 Apr;17(1):208-12.
          pmc: PMC2106263pubmed: 13986422doi: 10.1083/jcb.17.1.208google scholar: lookup
        18. RICHARDSON KC, JARETT L, FINKE EH. Embedding in epoxy resins for ultrathin sectioning in electron microscopy.. Stain Technol 1960 Nov;35:313-23.
          pubmed: 13741297doi: 10.3109/10520296009114754google scholar: lookup
        19. Wagner BA, Venkataraman S, Buettner GR. The rate of oxygen utilization by cells.. Free Radic Biol Med 2011 Aug 1;51(3):700-12.
        20. Goldman SJ, Taylor R, Zhang Y, Jin S. Autophagy and the degradation of mitochondria.. Mitochondrion 2010 Jun;10(4):309-15.
          pmc: PMC2874649pubmed: 20083234doi: 10.1016/j.mito.2010.01.005google scholar: lookup
        21. Ramkrishna V, Tiwari GP, Bhattacharya M, Saigal RP. Dehydrogenases in the epithelium of oesophagus and forestomach of adult buffalo. Ind J Anim Sci 1987;57:20-5.
        22. Soveri T, Lindberg LA. Histochemistry of the forestomach epithelium of the reindeer calf.. Acta Histochem 1993 Sep;95(1):117-24.
          pubmed: 8279231doi: 10.1016/s0065-1281(11)80397-1google scholar: lookup
        23. von Engelhardt W, Breves G. Physiologie der Haustiere. 3rd ed. Enke Publ., Stuttgart, Germany, 2009.
        24. Dodde RE, Bull JL, Shih AJ. Bioimpedance of soft tissue under compression.. Physiol Meas 2012 Jun;33(6):1095-109.
          pubmed: 22621935doi: 10.1088/0967-3334/33/6/1095google scholar: lookup
        25. Tornatore TF, Dalla Costa AP, Clemente CF, Judice C, Rocco SA, Calegari VC, Cardoso L, Cardoso AC, Gonçalves A Jr, Franchini KG. A role for focal adhesion kinase in cardiac mitochondrial biogenesis induced by mechanical stress.. Am J Physiol Heart Circ Physiol 2011 Mar;300(3):H902-12.
          pubmed: 21148763doi: 10.1152/ajpheart.00319.2010google scholar: lookup
        26. Schmitz G, Langmann T. Metabolic learning in the intestine: adaptation to nutrition and luminal factors.. Horm Metab Res 2006 Jul;38(7):452-4.
          pubmed: 16933181doi: 10.1055/s-2006-947841google scholar: lookup
        27. Millet S, Meyns T, Aluwé M, De Brabander D, Ducatelle R. Effect of grinding intensity and crude fibre content of the feed on growth performance and gastric mucosa integrity of growing-finishing pigs. Livestock Sci 2010;134:152-54.

        Citations

        This article has been cited 3 times.
        1. Martyniuk K, Ziółkowska N, Hanuszewska-Dominiak M, Szyryńska N, Lewczuk B. Histology and Ultrastructure of the Esophagus in European Beaver (Castor fiber) Displays Features Adapted to Seasonal Changes in Diet. Animals (Basel) 2023 Feb 11;13(4).
          doi: 10.3390/ani13040635pubmed: 36830422google scholar: lookup
        2. Malatesta M. Ultrastructural histochemistry in biomedical research: Alive and kicking. Eur J Histochem 2018 Nov 7;62(4).
          doi: 10.4081/ejh.2018.2990pubmed: 30418011google scholar: lookup
        3. Pellicciari C. Histochemistry in biology and medicine: a message from the citing journals. Eur J Histochem 2015 Dec 23;59(4):2610.
          doi: 10.4081/ejh.2015.2610pubmed: 26708189google scholar: lookup