Home Phenotypic variations in osmotic lysis of Sahel goat erythrocytes in non-ionic glucose media
Article
Licensed
Unlicensed Requires Authentication

Phenotypic variations in osmotic lysis of Sahel goat erythrocytes in non-ionic glucose media

  • Nanacha Afifi Igbokwe ORCID logo and Ikechukwu Onyebuchi Igbokwe EMAIL logo
Published/Copyright: December 2, 2015

Abstract

Background: Erythrocyte osmotic lysis in deionised glucose media is regulated by glucose influx, cation efflux, and changes in cell volume after water diffusion. Transmembrane fluxes may be affected by varied expression of glucose transporter protein and susceptibility of membrane proteins to glucose-induced glycosylation and oxidation in various physiologic states.

Methods: Variations in haemolysis of Sahel goat erythrocytes after incubation in hyposmotic non-ionic glucose media, associated with sex, age, late pregnancy, and lactation, were investigated.

Results: The osmotic fragility curve in glucose media was sigmoidal with erythrocytes from goats in late pregnancy (PRE) or lactation (LAC) or from kid (KGT) or middle-aged (MGT) goats. Non-sigmoidal phenotype occurred in yearlings (YGT) and old (OGT) goats. The composite fragility phenotype for males and non-pregnant dry (NPD) females was non-sigmoidal. Erythrocytes with non-sigmoidal curves were more stable than those with sigmoidal curves because of inflectional shift of the curve to the left. Erythrocytes tended to be more fragile with male than female sex, KGT and MGT than YGT and OGT, and LAC and PRE than NPD. Thus, sex, age, pregnancy, and lactation affected the haemolytic pattern of goat erythrocytes in glucose media.

Conclusions: The physiologic state of the goat affected the in vitro interaction of glucose with erythrocytes, causing variations in osmotic stability with variants of fragility phenotype. Variations in the effect of high extracellular glucose concentrations on the functions of membrane-associated glucose transporter, aquaporins, and the cation cotransporter were presumed to be relevant in regulating the physical properties of goat erythrocytes under osmotic stress.


Corresponding author: Ikechukwu Onyebuchi Igbokwe, Strategic Animal Research Group, Department of Veterinary Pathology, University of Maiduguri, P.O. Box 8000, Maiduguri, Nigeria, Phone: +234 834811622, E-mail:

Acknowledgments

Ismaila Gadaka, Chima V. Maduka, Alakpa B. Ikpe, and Sylvester Ogbaji provided technical and material assistance.

Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Inaba M, Messick JB. Erythrocyte membrane defects. In: Weiss DJ, Wardrop KJ, editors. Schalm’s veterinary hematology, 6th ed. Ames: Blackwell Publishing, 2010:187–95.Search in Google Scholar

2. Wright IG. Osmotic fragility of erythrocytes in acute Babesia argentina and Babesia bigemina infections in splectomized Bos taurus calves. Res Vet Sci 1973;15:299–305.10.1016/S0034-5288(18)33799-8Search in Google Scholar

3. Oyewale JO. Studies on the erythrocyte osmotic fragility of rats infected with Trypanosoma brucei. Anim Technol 1987;38:219–28.Search in Google Scholar

4. Mijares A, Vivas J, Abad C, Betancourt M, Piñero S, Proverbio F, et al. Trypanosoma evansi: effect of experimental infection on the osmotic fragility, lipid peroxidation and calcium-ATPase activity of rat red blood cells. Exp Parasitol 2010;124:301–5.10.1016/j.exppara.2009.11.002Search in Google Scholar

5. Kobo PI, Ayo JO, Aluwong T, Zezi AU, Maikai V, Ambali SF. Flavonoid mixture ameliorates increase in erythrocyte osmotic fragility and malondialdehyde concentration induced by Trypanosoma brucei brucei-infection in Wistar rats. Res Vet Sci 2014;96:139–42.10.1016/j.rvsc.2013.10.005Search in Google Scholar

6. Silva IM, Hubsch C, Ysern-Caldentey M. Erythrocyte osmotic fragility and cation concentrations during experimentally induced bovine anaplasmosis. Comp Biochem Physiol Part A: Physiol 1989;94:455–9.10.1016/0300-9629(89)90120-5Search in Google Scholar

7. Jain NC. Essentials of veterinary hematology. Philadelphia: Lea and Febiger, 1989:203–6.Search in Google Scholar

8. Ambali SF, Ayo JO, Ojo SA, Esievo KA. Ameliorative effect of vitamin C on chlorpyrifos-induced increased erythrocyte fragility in Wistar rats. Hum and Exp Toxicol 2010;30:19–24.10.1177/0960327110368415Search in Google Scholar

9. Lessler MA, Walters MI. Erythrocyte osmotic fragility in the presence of lead or mercury. Exp Biol Med 1973;142:548–53.10.3181/00379727-142-37064Search in Google Scholar

10. Parpart AK, Lorenz PB, Parpart ER, Gregg JR, Chase AM. The osmotic resistance (fragility) of human red cells. J Clin Invest 1947;26:636–40.10.1172/JCI101847Search in Google Scholar

11. Igbokwe NA, Igbokwe IO. Influence of extracellular media’s ionic strength on the osmotic stability of Sahel goat erythrocytes. J Basic Clin Physiol Pharmacol 2015;26:171–9.10.1515/jbcpp-2014-0014Search in Google Scholar

12. Jandl JH. Leaky red cells. Blood 1965;26:367–82.10.1182/blood.V26.3.367.367Search in Google Scholar

13. Greene NM. Glucose permeability of human erythrocytes and effects of inhalation anesthetics, oxygen and carbon dioxide. Yale J Biol Med 1965;37:319–30.Search in Google Scholar

14. Morrison AD, Clement RS, Travis SB, Oski F, Winegrad AI. Glucose utilization by the polyol pathway in human erythrocytes. Biochem Biophys Res Commun 1970;40: 199–205.10.1016/0006-291X(70)91066-1Search in Google Scholar

15. Guarner V, Alvarez-Buylla R. Erythrocyte and glucose homeostasis in rats. Diabetes 1989;38:410–5.10.2337/diab.38.4.410Search in Google Scholar PubMed

16. Murphy JR. Erythrocyte metabolism: III. Relationship of energy metabolism and serum factors to the osmotic fragility following incubation. J Lab Clin Med 1962;60:86–109.Search in Google Scholar

17. Zinchuk VV. Erythrocyte deformability: physiological aspects. Usp Fiziol Nauk 2001;32:66–78.Search in Google Scholar

18. Simmons NL, Naftalin RJ. Membrane and intracellular modes of sugar-dependent increments in red cell stability. Biochim Biophys Acta 1967;419:493–511.10.1016/0005-2736(76)90261-3Search in Google Scholar

19. Riquelme B, Foresto P, D’Arrigo M, Valverde J, Rasia R. A dynamic and stationary rheological study of erythrocytes incubated in a glucose medium. J Biochem Biophys Methods 2005;62:131–41.10.1016/j.jbbm.2004.10.004Search in Google Scholar

20. Quan GB, Han Y, Yang C, Hu WB, Liu MX, Liu A, et al. Inhibitory effect of trehalose on phosphatidylserin exposure, osmotic fragility and membrane lipid peroxidation damage of erythrocytes induced by high concentration of glucose. Zhongguo ShiYan Xue Ye Xue Za Zhi 2008;16:1442–6.Search in Google Scholar

21. Babu N, Singh M. Influence of hyperglycemia on aggregation, deformability and shape parameters of erythrocytes. Clin Hemorheol Microcirc 2004;31:273–80.Search in Google Scholar

22. Kung C-M, Tseng Z-L, Wang H-L. Erythrocyte fragility increases with level of glycosylated hemoglobin in type 2 diabetic patients. Clin Hemorheol Microcirc 2009;43:345–51.10.3233/CH-2009-1245Search in Google Scholar

23. Shin S, Ku YH, Suh JS, Singh M. Rheological characteristics of erythrocytes incubated in glucose media. Clin Hemorheol Microcirc 2008;38:153–61.Search in Google Scholar

24. Traykov TT, Jain RK. Effect of glucose and galactose on red cell membrane deformability. Int J Microcirc Clin Exp 1987;6:35–44.Search in Google Scholar

25. Jain SK. Hyperglycermia can cause membrane lipid peroxidation and osmotic fragility in human red blood cells. J Biol Chem 1989;264:21340–5.10.1016/S0021-9258(19)30085-7Search in Google Scholar

26. Caimi G, Serra A, Presti RL. Red cell calcium accumulation (total and cytosolic) and erythrocyte membrane fluidity in several clinical conditions. Clin Hemorheol 1993;13:227–35.10.3233/CH-1993-13207Search in Google Scholar

27. Lösche W, Michael E, Lull K, Kreutzfeld B, Heptinstall S, Till U. The effect of high glucose concentrations on the osmotic and mechanical resistance of human erythrocytes. Z Med Lab Diagn 1989;30:124–7.Search in Google Scholar

28. Travis SF, Morrison AD, Clements RS, Winegrad AI, Oski FA. Metabolic alterations in the human erythrocyte produced by increases in glucose concentration: the role of the polyol pathway. J Clin Invest 1971;50:2105–12.10.1172/JCI106704Search in Google Scholar PubMed PubMed Central

29. Matsuzawa T, Ikarashi Y. Haemolysis of various mammalian erythrocytes in sodium chloride, glucose and phosphate-buffer solutions. Lab Anim 1979;13:329–31.10.1258/002367779780943297Search in Google Scholar PubMed

30. Lemos GS, Márquez-Bernardes LF, Arvelos LR, Paraíso LF, Penha-Silva N. Influence of glucose concentration on the membrane stability of human erythrocytes. Cell Biochem Biophys 2011;61:531–7.10.1007/s12013-011-9235-zSearch in Google Scholar PubMed

31. Schalm OW, Jain NC, Caroll EJ. Veterinary hematology, 3rd ed. Philadelphia: Lea and Febiger, 1975.Search in Google Scholar

32. Glaji YA, Mani AU, Igbokwe IO. Relationship of faecal egg count with packed cell volume and anaemia in Sahel sheep and goats in semi-arid northeastern Nigeria. Comp Clin Pathol 2014;23:1195–201.10.1007/s00580-013-1762-0Search in Google Scholar

33. Waziri MA, Ribadu AY, Sivachelvan N. Changes in the serum proteins, hematological and serum biochemical profiles in the gestation period in Sahel goats. Vet Arhiv 2010;80:215–24.Search in Google Scholar

34. Herdt T. Gastrointestinal physiology and metabolism. In: Cunningham JG, editor. Textbook of veterinary physiology. 2nd ed. Philadelphia: WB Saunders, 1997:379–80.Search in Google Scholar

35. Sandabe UK, Mustapha AR, Sambo EY. Effect of pregnancy on some biochemical parameters of parameters in Sahel goats in semi-arid zones. Vet Res Commun 2004;28:279–85.10.1023/B:VERC.0000026655.69812.79Search in Google Scholar

36. Hocquette J-F, Abe H. Facilitative glucose transporters in livestock species. Reprod Nutr Dev 2000;40:517–33.10.1051/rnd:2000134Search in Google Scholar

37. Harik SI, Behmand RA, Arafah BM. Chronic hyperglycemia increases the density of glucose transporters in human erythrocyte membranes. J Clin Endocrinol Metab 1991;72:814–8.10.1210/jcem-72-4-814Search in Google Scholar PubMed

38. Xie WS, Yuc JC, Tu YP. Fluorescence study on ligand induced conformational changes of human erythrocyte glucose transporter. Biochem Mol Biol Int 1996;39:279–84.10.1080/15216549600201291Search in Google Scholar

39. Hu XJ, Peng F, Zhou HQ, Zhang ZH, Cheng WY, Feng HF. The abnormality of glucose transporter in the erythrocyte membrane of Chinese type 2 diabetic patients. Biochim Biophys Acta 2000;1466:306–14.10.1016/S0005-2736(00)00175-9Search in Google Scholar

40. Stockham SL, Scott MA. Fundamentals of veterinary clinical pathology, 2nd ed. Ames: Blackwell, 2008:707–37.Search in Google Scholar

Received: 2015-4-2
Accepted: 2015-9-30
Published Online: 2015-12-2
Published in Print: 2016-3-1

©2016 by De Gruyter

Downloaded on 9.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jbcpp-2015-0036/html
Scroll to top button