Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1976 Nov;262(2):447–458. doi: 10.1113/jphysiol.1976.sp011604

Permeability of individual human erythrocytes to thiourea.

A W Jay
PMCID: PMC1307652  PMID: 994044

Abstract

The osmotic swelling to haemolysis of individual red blood cells by isosmotic thiourea has been studied using microcine photography. 2. Crenation occurs immediately upon addition of isosmotic thiourea. The cell becomes a crenated sphere without volume decrease. 3. Subsequently, the cell volume increases linearly with time with maximum swelling occurring at about 102 sec which is 81% of the total haemolysis time. 4. At maximum swelling, the cell volume is 92% greater than the initial cell volume. This volume increase is about double that measured with other permeating substances. 5. The much larger maximum volume implies that thiourea increases the area of the cell membrane. This increase varies from 0 to 75% for individual cells, with a mean of 22%. 6. Membrane expansion varies inversely as the initial cell membrane area and cell volume (r=0-790). 7. Using the increased surface area, increased maximum volume and the swelling time, the mean permeability is calculated to be 5-52 X 10(-7) cm/sec (S.D. of mean=+/-1-19 X 10(-7) cm/sec). The distribution of permeabilities represents a normal distribution. 8. The pre-lytic potassium loss ranged from 0 to 36% with a mean value of 16-5%. This is consistent with values reported in the literature for slow haemolysis. As with other permeants the distribution is skewed towards lower values. 9. Membrane permeability of individual cells varies with the amount of membrane expansion observed. Coefficient of correlation between permeability and expansion index is 0-674. 10. There is no correlation between permeability and the reciprocal of the haemolysis time (r=-0-035). The correlation between permeability and the reciprocal of the swelling time is also poor (r=0-303), probably owing to the variability in membrane expansion by thiourea in individual cells. 11. As has been shown previously for faster permeants, the permeability coefficient cannot be calculated from the haemolysis time. Because thiourea alters the membrane area and the haemolytic volume, the coefficient cannot be calculated from the swelling time unless the changes in the membrane area are also taken into account.

Full text

PDF
447

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BERLIN N. I., WALDMANN T. A., WEISSMAN S. M. Life span of red blood cell. Physiol Rev. 1959 Jul;39(3):577–616. doi: 10.1152/physrev.1959.39.3.577. [DOI] [PubMed] [Google Scholar]
  2. BERNSTEIN R. E. Alterations in metabolic energetics and cation transport during aging of red cells. J Clin Invest. 1959 Sep;38:1572–1586. doi: 10.1172/JCI103936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DANON D., MARIKOVSKY V. DETERMINATION OF DENSITY DISTRIBUTION OF RED CELL POPULATION. J Lab Clin Med. 1964 Oct;64:668–674. [PubMed] [Google Scholar]
  4. DANON D. Osmotic hemolysis by a gradual decrease in the ionic strength of the surrounding medium. J Cell Comp Physiol. 1961 Apr;57:111–117. doi: 10.1002/jcp.1030570208. [DOI] [PubMed] [Google Scholar]
  5. Jay A. W. Geometry of the human erythrocyte. I. Effect of albumin on cell geometry. Biophys J. 1975 Mar;15(3):205–222. doi: 10.1016/S0006-3495(75)85812-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Jay A. W., Rowlands S. The stages of osmotic haemolysis. J Physiol. 1975 Nov;252(3):817–832. doi: 10.1113/jphysiol.1975.sp011172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Roth S., Seeman P. All lipid-soluble anaesthetics protect red cells. Nat New Biol. 1971 Jun 30;231(26):284–285. doi: 10.1038/newbio231284a0. [DOI] [PubMed] [Google Scholar]
  8. Saari J. T., Beck J. S. Hypotonic hemolysis of human red blood cells: a two-phase process. J Membr Biol. 1975;23(3-4):213–226. doi: 10.1007/BF01870251. [DOI] [PubMed] [Google Scholar]
  9. Saari J. T., Beck J. S. Probability density function of the red cell membrane permeability coefficient. Biophys J. 1974 Jan;14(1):33–45. doi: 10.1016/S0006-3495(74)85901-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Seeman P., Sauks T., Argent W., Kwant W. O. The effect of membrane-strain rate and of temperature on erythrocyte fragility and critical hemolytic volume. Biochim Biophys Acta. 1969;183(3):476–489. doi: 10.1016/0005-2736(69)90162-x. [DOI] [PubMed] [Google Scholar]
  11. Seeman P. The membrane actions of anesthetics and tranquilizers. Pharmacol Rev. 1972 Dec;24(4):583–655. [PubMed] [Google Scholar]
  12. WESTERMAN M. P., PIERCE L. E., JENSEN W. N. ERYTHROCYTE LIPIDS: A COMPARISON OF NORMAL YOUNG AND NORMAL OLD POPULATIONS. J Lab Clin Med. 1963 Sep;62:394–400. [PubMed] [Google Scholar]
  13. Yaari A. Mobility of human red blood cells of different age groups in an electric field. Blood. 1969 Feb;33(2):159–163. [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES