Analyze Diet
Veterinary medicine international2009; 2010; 987309; doi: 10.4061/2010/987309

Changes in Adenylate Nucleotides Concentration and Na, K-ATPase Activities in Erythrocytes of Horses in Function of Breed and Sex.

Abstract: The aim of this study was to examine the relationships between the concentrations of ATP, ADP, AMP (HPLC methods), total nucleotide pool (TAN), adenylate energy charge (AEC) and Na(+), K(+)-ATPase erythrocytic activities (by Choi's method) of horses as a function of breed and sex. The studies were conducted on 54 horses (stallions and mares) of different constitution types: breathing constitution (Wielkopolska and Hanoverian breed) and digestive constitution (Ardenian breed). Horse erythrocytes, independently of examined breed, present low ATP concentration in comparison to other mammal species while retaining relatively high AEC. Erythrocytes of breathing constitution type horses appear to have a more intensive glucose metabolism and a more efficient energetic metabolism when compared to digestive constitution type horses. The conclusions may be proven by significantly higher ATP concentration, higher TAN and significantly higher AEC in breathing constitution type horses compared to the digestive constitution type. Sex does not significantly influence adenine nucleotides concentration in the erythrocytes of the examined horses, however, stallions have slightly higher values in comparison to mares. A positive correlation was found between Na(+), K(+), -ATPase activity, ATP, ADP and AMP concentration and TAN in Wielkopolska and Ardenian breeds, which was not confirmed for the Hanoverian breed.
Publication Date: 2009-11-11 PubMed ID: 20445796PubMed Central: PMC2859025DOI: 10.4061/2010/987309Google 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.

This research study investigates the differences in ATP, ADP, AMP concentrations and Na(+), K(+)-ATPase activities in the red blood cells (erythrocytes) of different horse breeds, based on their constitution type (breathing or digestive), and sex. It concludes that breathing constitution type horses have a more efficient energy metabolism than digestive constitution types, and that sex does not significantly affect these measurements in the studied horses.

Research Methodology

  • The study was conducted using 54 horses of different breed and sex, divided into breathing constitution types (represented by Wielkopolska and Hanoverian breeds) and digestive constitution types (represented by the Ardenian breed).
  • For each horse, concentrations of ATP, ADP, and AMP in their erythrocytes were measured using high performance liquid chromatography (HPLC) methods.
  • The total adenylate nucleotide pool (TAN) – the sum of all these molecules – and the adenylate energy charge (AEC) – a measure of cell energy status – were calculated.
  • The activity of the enzyme Na(+), K(+)-ATPase within the horse’s erythrocytes was also evaluated using Choi’s method. This enzyme is responsible for managing the concentration of sodium and potassium ions within the cells.

Key Findings

  • Horses, regardless of breed, have lower ATP concentrations in their erythrocytes compared to other mammalian species, but maintain relatively high AEC, indicating efficient energy metabolism.
  • Breathing constitution type horses have a more intensive glucose metabolism and a more efficient energetic metabolism when compared to digestive constitution type horses. This is demonstrated by their significantly higher ATP concentration, higher TAN, and significantly higher AEC.
  • Sex does not significantly influence the concentration of adenine nucleotides in the erythrocytes of horses, although stallions had slightly higher measurements than mares.
  • The study found a positive correlation between Na(+), K(+), -ATPase activity, ATP, ADP and AMP concentration, and TAN in Wielkopolska and Ardenian breeds. This correlation was not confirmed for the Hanoverian breed.

Conclusion

  • The findings of this study provide valuable insight into understanding the metabolic differences between horses of different constitution types and breeds. It could have potential implications for nutritional planning and health management of horses, geared to their specific breed and constitutional type characteristics.
  • The fact that sex does not significantly influence these metabolic parameters is also interesting, suggesting that, in some aspects, energy metabolism in horses may not be significantly influenced by gender.

Cite This Article

APA
Suska M, Skotnicka E. (2009). Changes in Adenylate Nucleotides Concentration and Na, K-ATPase Activities in Erythrocytes of Horses in Function of Breed and Sex. Vet Med Int, 2010, 987309. https://doi.org/10.4061/2010/987309

Publication

ISSN: 2042-0048
NlmUniqueID: 101524203
Country: United States
Language: English
Volume: 2010
Pages: 987309

Researcher Affiliations

Suska, Maria
  • Department of Physiology, Faculty of Life Sciences, University of Szczecin, Piastów 40 B, av, bl. 6, 71-065 Szczecin, Poland.
Skotnicka, Ewa

    References

    This article includes 40 references
    1. Dudzińska W, Hłyńczak AJ. Purine nucleotides of human erythrocytes—metabolism and regulation.. Postepy Biochemii 2004;50(4):353–362.
      pubmed: 15957530
    2. Dudzińska W, Hłyńczak AJ, Skotnicka E, Suska M. The purine metabolism of human erythrocytes.. Biochemistry 2006;71(5):467–475.
      pubmed: 16732723
    3. Ataullakhanov FI, Vitvitskii VM, Komarova SV, Mosharov EV. Energy-dependent processes and adenylate metabolism in human erythrocytes.. Biochemistry 1996;61(2):197–203.
      pubmed: 8717495
    4. Fokina KV, Yazykova MY, Danshina PV, Schmalhausen EV, Muronetz VI. Participation of glyceraldehyde-3-phosphate dehydrogenase in the regulation of 2,3-diphosphoglycerate level in erythrocytes.. Biochemistry 2000;65(4):463–468.
      pubmed: 10810185
    5. Arai T, Washizu T, Sagara M. D-glucose transport and glycolytic enzyme activities in erythrocytes of dogs, pigs, cats, horses, cattle and sheep.. Research in Veterinary Science 1995;58(2):195–196.
      pubmed: 7761703
    6. Brugnara C. Erythrocyte membrane transport physiology.. Current Opinion in Hematology 1997;4(2):122–127.
      pubmed: 9107529
    7. Hoffman JF. ATP compartmentation in human erythrocytes.. Current Opinion in Hematology 1997;4(2):112–115.
      pubmed: 9107527
    8. Siems WG, Sommerburg O, Grune T. Erythrocyte free radical and energy metabolism.. Clinical Nephrology 2000;53(supplement 1):S9–S17.
      pubmed: 10746800
    9. Bennett V, Baines AJ. Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues.. Physiological Reviews 2001;81(3):1353–1392.
      pubmed: 11427698
    10. Joshi A, Palsson BO. Metabolic dynamics in the human red cell—part IV: data prediction and some model computations.. Journal of Theoretical Biology 1990;142(1):69–85.
      pubmed: 2141094
    11. Harvey JW. The erythrocyte: physiology, metabolism, and biochemical disordes.. In: Kalenko JJ, Harvey JW, Bruss ML, editors. Clinical Biochemistry of Domestic Animals. New York, NY, USA: Academic Press; 1997. pp. 125–142.
    12. Traut TW. Physiological concentrations of purines and pyrimidines.. Molecular and Cellular Biochemistry 1994;140(1):1–22.
      pubmed: 7877593
    13. Brommer H, Sloet Van Oldruitenborgh-Oosterbaan MM, Kessels B. Haematological and blood biochemical characteristics of dutch warmblood foals managed under three different rearing conditions from birth to 5 months of age.. Veterinary Quarterly 2001;23(2):92–95.
      pubmed: 11361107
    14. Suska M, Skotnicka E, Dudzińska W, Orowicz W, Brzezińska M. Adenylate nucleotides and 2,3-biphosphoglycerate concentration in erythrocytes of growing Wielkopolska stallions.. Acta Veterinaria Brno 2006;75(1):13–20.
    15. Suska M. The effect of sodium fluoride on the adenine nucleotide pool in erythrocytes of wistar rats.. International Journal of Occupational Medicine and Environmental Health 2001;14(4):369–373.
      pubmed: 11885920
    16. Suska M. Energy metabolism of erythrocytes in lambs chronically exposed to fluorine compounds.. Acta Veterinaria Brno 2002;71(3):313–317.
    17. Dudzińska W, Hłyńczak AJ. Purine nucleotides and their metabolites in erythrocytes of streptozotocin diabetic rats.. Diabetes and Metabolism 2004;30(6):557–567.
      pubmed: 15671926
    18. Skotnicka E, Baranowska-Bosiacka I, Dudzińska W. The effect of exhaustive exercise on the concentration of purine nucleotides and their metabolites in erythrocytes.. Biology of Sport 2008;25(1):35–55.
    19. Smolenski RT, Lachno DR, Ledingham SJM, Yacoub MH. Determination of sixteen nucleotides, nucleosides and bases using high-performance liquid chromatography and its application to the study of purine metabolism in hearts for transplantation.. Journal of Chromatography 1990;527(2):414–420.
      pubmed: 2387888
    20. Choi SJ, Taylor MA, Abrams R. Depression, ECT, and erythrocyte adenosinetriphosphatase activity.. Biological Psychiatry 1977;12(1):75–81.
      pubmed: 138451
    21. Goldenberg H, Fernandez A. Simplified method for the estimation of inorganic phosphorus in body fluids.. Clinical Chemistry 1966;12(12):871–882.
      pubmed: 5926907
    22. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ. Protein measurment Folin with the fend reagent.. The Journal of Biological Chemistry 1951;193:256–267.
      pubmed: 14907713
    23. Atkinson DE. The energy charge of the adenylate pool as a regulatory parameter. Interaction with feedback modifiers.. Biochemistry 1968;7(11):4030–4034.
      pubmed: 4972613
    24. Dębski B. The effect of training and physical exercise on the energetic metabolism of equine erythrocytes.. Zentralblatt für Veterinärmedizin. Reihe A 1985;32(3):190–195.
      pubmed: 3923737
    25. Miseta A, Bogner P, Berenyi E. Relationship between cellular ATP, potassium, sodium and magnesium concentrations in mammalian and avian erythrocytes.. Biochimica et Biophysica Acta 1993;1175(2):133–139.
      pubmed: 8418892
    26. Stankiewicz W. Veterinary Haematology.. Warszawa, Poland: PZWiL; 1972.
    27. Leyko W, Bartosz G, Duda W, Wojtkowiak Z, Kołątaj A. The content of nucleotides in erythrocytes of different breeds of cattle.. Genetica Polonica 1974;15(1-2):91–96.
    28. Harvey JW, Kaneko JJ. Glucose metabolism of mammalian erythrocytes.. Journal of Cellular Physiology 1976;89(2):219–223.
      pubmed: 987042
    29. Fujii S, Beutler E. High glucose concentrations partially release hexokinase from inhibition by glucose 6-phosphate.. Proceedings of the National Academy of Sciences of the United States of America 1985;82(5):1552–1554.
      pmc: PMC397302pubmed: 3856279
    30. Janiak M, Suska M, Dudzińska W, Skotnicka E. Blood glutathione status and activity of glutathione-metabolizing antioxidant enzymes in erythrocytes of young trotters in basic training.. Journal of Animal Physiology and Animal Nutrition In press.
      pubmed: 19364380
    31. Zeleznikar RJ, Dzeja PP, Goldberg ND. Adenylate kinase-catalyzed phosphoryl transfer couples ATP utilization with its generation by glycolysis in intact muscle.. The Journal of Biological Chemistry 1995;270(13):7311–7319.
      pubmed: 7706272
    32. Ramsey JM, Pipoly SW. Jr.. Response of erythrocytic 2,3-diphosphoglycerate to strenuous exercise.. European Journal of Applied Physiology and Occupational Physiology 1979;40(4):227–233.
      pubmed: 34512
    33. Fokina KV, Dainyak MB, Nagradova NK, Muronetz VI. A study on the complexes between human erythrocyte enzymes participating in the conversions of 1,3-diphosphoglycerate.. Archives of Biochemistry and Biophysics 1997;345(2):185–192.
      pubmed: 9308888
    34. Mulquiney PJ, Bubb WA, Kuchel PW. Model of 2,3-bisphosphoglycerate metabolism in the human erythrocyte based on detailed enzyme kinetic equations: in vivo kinetic characterization of 2,3-bisphosphoglycerate synthase/phosphatase using 13C and 31P NMR.. Biochemical Journal 1999;342(3):567–580.
      pmc: PMC1220498pubmed: 10477268
    35. Lasker N, Hopp L, Grossman S, Bamforth R, Aviv A. Race and sex differences in erythrocyte Na+, K+, and Na+-K+-adenosine triphosphatase.. The Journal of Clinical Investigation 1985;75(6):1813–1820.
      pmc: PMC425536pubmed: 2989333
    36. Canestrari F, Galli F, Boschi S. Erythrocyte Na+,K+-ATPase properties and adenylate energy charge in normotensives and in essential hypertensives.. Clinica Chimica Acta 1994;224(2):167–179.
      pubmed: 8004787
    37. Apell H-J, Nelson MT, Marcus MM, Lauger P. Effects of the ATP, ADP and inorganic phosphate on the transport rate of the Na+,K+-pump.. Biochimica et Biophysica Acta 1986;857(1):105–115.
      pubmed: 3008841
    38. Ling GN. Explaining on request a correlation between membrane Na+,K+-ATPase and K+ content in erythrocytes and other findings in the preceding paper.. Physiological Chemistry and Physics and Medical NMR 1998;30(1):89–97.
      pubmed: 9807237
    39. Pedersen PL. Transport ATPases in biological systems and relationship to human disease: a brief overview.. Journal of Bioenergetics and Biomembranes 2002;34(5):327–332.
      pubmed: 12539959
    40. Udziela M. Sodium and potassium concentrations in erythrocytes and blood plasma of young women in differential physiological state.. Wiadomosci Lekarskie 1968;21(21):1905–1908.
      pubmed: 5714922