Impact of thermohaemolysis-associated membrane alteration on the passive ion permeability and life-span of erythrocytes

Journal of Thermal Biology

Volumn 24, Issue 2, 1999, Pages 143-150

  Ivanov, I T ^a  

^a Trakia University Medical College   (Bulgaria)

Author keywords

Erythrocyte life span; Mammalian erythrocytes; Passive ion permeability; Sphingomyelin; Thermal resistance

Indexed keywords

EID: 0032911455     PISSN: 03064565     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4565(99)00003-0     Document Type: Article

References (32)

1. Brummen M., Heinrich R. ByoSystems. 17:1984;155-169.
2. Brunner J., Graham D.E., Hauser M., Semenza G. Ion and sugar permeability of lecithin bilayers: Comparison of curved and planar bilayers. J. Membr. Biol. 57:1980;133-141.
3. Burwell E.L., Brickley B., Finch C.A. Erythrocyte life-span in small animals. Comparison of two methods employing radioiron. Amer. J. Physiology. 172:1952;718-724.
4. Christian J.A., Rebar A.H., Boon G.D., Low P.S. Methodologic considerations for the use of canine in vivo aged erythrocytes biotinylated erythrocytes to study red blood cell senescence. Exp. Hematol. 24:1996;82-88.
5. Deuticke B. Properties and structural basis of simple diffusion pathways in the erythrocyte membrane. Rev. Physiol. Biochem. Pharmac. 78:1977;1-97.
6. Erdmann E., Bernhardt I., Herrmann A., Glaser R. Species-dependent differences in the influence of ionic strength on potassium transport of erythrocytes. The role of membrane fluidity and Ca. Gen. Physiol. Biophys. 9:1990;577-588.
7. George J.W., Duncan J.R., Mahaffey E.A. Comparison of pyrimidine 5′-nucleotidase activity in erythrocytes of sheep, dogs, cats, horses, calves, and Mongolian gerbils. Am. J. Vet. Res. 44:(10):1983;1968-1970.
8. Gershfeld N.L., Murayama M. Thermal instability of red blood cell membrane bilayers: temperature dependence of thermolysis. J. membr. Biol. 101:1988;67-72.
9. Gordiyenco O.I., Gordiyenco E.A. Effects of temperature and the ionic strength of the medium on passive permeability of erythrocyte membranes to potassium ions. Biol. membr. 3:1986;869-872.
10. Inaba M., Naede Y. Correlation between protein 4.1a/4.1b ratio and erythrocyte life span. Biochim. Biophys. Acta. 944:(2):1988;256-264.
11. Ivanov I.T. Thermohaemolysis of human erythrocytes in sucrose containing isotonic media. J. Therm. Biol. 17:1992;375-379.
12. Ivanov I.T., Benov C. Thermohaemolysis of human erythrocytes in isotonic NaCl/sucrose media during transient heating. J. therm. Biol. 17:1992;375-379.
13. Ivanov I.T. Thermohaemolysis of mammalian erythrocytes. J. Therm. Biol. 18:1993;177-183.
14. Ivanov, I.T., Todorova, R., Zlatanov, I., 1999. Microcalorimetric and spectrofluorometric study of thermohemolysis related membrane alteration, Int. J. Hyperthermia 15, 29-43.
15. Jindal H.K., Ai Z., Gascard P., Horton C., Cohen C.M. Specific loss of protein kinase activity in senescent erythrocytes. Blood. 88:1996;1479-1487.
16. Kirk R.G. Potassium transport and lipid composition in mammalian red blood cell membranes. Biochim. Biophys. Acta. 464:1977;157-164.
17. Kolekov A.N., Parshutin G.V. Physiology of Livestock. 1980;22 Kolos Publishing House, Moscow. (in Russian).
18. Komeno T., Ninomiya H., Itoh T., Fujita T., Nagasawa T. Hemolytic anemia associated with myotic muscular dystrophy. Int. Med. 35:1996;746-748.
19. Kurata M., Suzuki M., Agar N.S. Antioxidant systems and erythrocyte life-span in mammals. Comp. Biochem. Physiol. B. 106:1993;477-487.
20. Lepock J., Frey H., Bayne H., Markus J. Relationship of hyperthermia-induced hemolysis of human erythrocytes to the thermal denaturation of membrane proteins. Biochim. Biophys. Acta. 980:1989;191-201.
21. Levtov V.A., Regirer S.A., Shadrina N.H. Rheology of Blood. 1982;68 Moscow Medicine. (in Russian).
22. Nichols J.W., Hitl M.W., Bangham A.D., Deamer D.W. Measurement of net proton-hydroxyl permeability of large unilateral liposomes with the fluorescent pH probe, 9-aminoacridine. Biochim. Biophys. Acta. 596:1980;393-403.
23. Papahadjopoulos D., Bangham A.D. Biophysical properties of phospholipids. II. Permeability of phosphatidyleserine liquid crystals to univalent ions. Biochim. Biophys. Acta. 126:1966;185-188.
24. Papahadjopoulos D., Nir S., Ohki S. Permeability properties of phospholipid membranes: Effect of cholesterol and temperature. Biochim. Biophys. Acta. 266:1972;561-583.
25. Parola, A.H., 1993. Membrane lipid-protein interactions. In: Shinitzky, M. (Ed.). Biomembranes. Physical Aspects, Chapter 5. VCH Verlagsgesellschaft mbH, D6940 Weinheim, pp. 159-277.
26. Prankerd T.A.J. The Red Cell. An Account of its Chemical Physiology and Pathology. 1960;167 C.C. Thomas publisher. Springfield, Illinois, USA.
27. Shinozuka T. Changes in human red blood cells during ageing in vivo. Key J. Med. 43:1994;155-163.
28. 50Cr-labeled erythrocytes in neonatal foals. J. Vet. Intern. Med. 6:(3):1992;183-185.
29. Stein W.D. The Movement of Molecules Across Membranes. 1967;47 Academic Press, N.Y.
30. Tsolov V., Tsolov A., Tsankov R. Enterohepatic cycle of the bile acids and the lifespan of erythrocytes. Vet. Med. Nauki. 22:(6):1985;27-33. (in Bulgarian).
31. Valberg L.S., Card R.T., Paulson E.J., Szivek J. The metal composition of erythrocytes in different species and its relationship to the lifespan of the cells in circulation. Comp. Biochem. Physiol. 15:1963;347-359.
32. Young A.J., Hay J.B. Rapid turnover of the reticulating lymphocyte pool in vivo. Int. J. Immunol. 7:1995;607-1615.