Osmotic properties of the erythrocyte. VII. The temperature coefficients of certain hemolytic processes

Jacobs, M. H.; Glassman, Harold N.; Parpart, Arthur K.

doi:10.1002/jcp.1030070205

Cited by 129 publications

(30 citation statements)

References 18 publications

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“…3 the possible relation is demonstrated between the permeability to glycerol and the concentration of oleic acid, one of the most conspicuous acids'. Here can be seen that also the hemolysis time of horse erythrocytes in an isotonic solution of glycerol, given by JACOBS et al 14 in an older publication, is in accord with the parallel found between permeability and fatty acid composition of the lipid moiety of the studied membranes.…”

Section: Discussionsupporting

confidence: 82%

Metabolism and functions of phosphatides specific fatty acid composition of the red blood cell membranes

Kögl

Gier

Mulder

et al. 1960

Biochimica et Biophysica Acta

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SUMMARYIn attempting to establish a specific lipid composition of biological interfaces, the fatty acid composition of the lipid moiety of the red cell membrane of a number of mammals was determined by means of gas-liquid chromatography. A rather constant and characteristic fatty acid pattern proved to occur in the membranes of the red cells of each species. Quantitatively striking differences were found between the fatty acid compositions of the red cell membranes of the various mammals. Most pronounced were differences in the palmitic acid and oleic acid content. A gradual decrease in the ratio palmitic acid-oleic acid was shown in the red cell membranes of: rat, man, rabbit, pig, horse, ox and sheep in that order. Since this arrangement rather resembled the sequence based on permeability properties of these membranes taken from the literature, a possible relationship between fatty acid composition and permeability of membranes is discussed.

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Section: Discussionsupporting

confidence: 82%

Metabolism and functions of phosphatides specific fatty acid composition of the red blood cell membranes

Kögl

Gier

Mulder

et al. 1960

Biochimica et Biophysica Acta

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“…This has been confirmed experimentally by Jacobs, Glassman & Parpart (1935), who have also shown that when the erythrocytes of one species are less permeable to a given substance than are the cells of a second species, the temperature coefficient of penetration in the former is greater than in the latter. The effect is not great, and their tables suggest that, as a very rough approximation, a fivefold decrease in cell permeability may be associated with a 25 % increase in the temperature coefficient.…”

Section: Effects Of Chelating and Other Agentsmentioning

confidence: 57%

Calcium ions and the permeability of human erythrocytes

Bolingbroke¹,

Maizels²

1959

The Journal of Physiology

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“…According to their hypothesis the temperature coefficient of permeability is negatively correlated with the absolute rate of permeation, so that rapidly penetrating molecules show a lower Arrhenius activation energy than slowly penetrating molecules, a consequence of the shape of the Boltzmann distribution of kinetic energy. Reasonable agreement with these predictions has been found in a number of red cell species for the transport of various non-electrolytes (Jacobs, Glassman & Parpart, 1935), but the uniformly high values of the temperature coefficients for inorganic anion transport show clearly that the theory does not hold for anion transport in red cells.…”

Section: Intracellular Adsorption Of Anionsmentioning

confidence: 72%

Temperature dependence of chloride, bromide, iodide, thiocyanate and salicylate transport in human red cells

Dalmark¹,

Wieth²

1972

The Journal of Physiology

214

138

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4. The rate of self-exchange of bromide, thiocyanate, and iodide between human red cells and media was determined after washing and labelling cells in media containing 120 mm bromide, thiocyanate, or iodide respectively. The rate of self-exchange of the three anions were 12, 3, and 0 4 % of the rate of chloride self-exchange found in the chloride medium.5. The Arrhenius activation energies of the self-exchange of bromide, iodide, and thiocyanate were all between 29 and 37 keal/mole, the same magnitude as found for the self-exchange of chloride.6. Although approximately 40 % of the intracellular iodide and salicylate ions appeared to be adsorbed to intracellular proteins, the rate of tracer anion efflux followed first order kinetics until at least 98 % of the intracellular anions had been exchanged. MADS DALMIARK AND JENS OTTO WIETH 7. The self-exchange of salicylate across the human red cell membrane occurred by a different mechanism than the one utilized by the inorganic monovalent anions. The activation energy of salicylate exchange (13.2 kcal/mole) was significantly lower than that of inorganic anion exchange. Salicylate exchange increased with decreasing pH in contrast to the exchange of chloride, which decreases when pH is lowered.

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Osmotic properties of the erythrocyte. VII. The temperature coefficients of certain hemolytic processes

Cited by 129 publications

References 18 publications

Metabolism and functions of phosphatides specific fatty acid composition of the red blood cell membranes

Metabolism and functions of phosphatides specific fatty acid composition of the red blood cell membranes

Calcium ions and the permeability of human erythrocytes

Temperature dependence of chloride, bromide, iodide, thiocyanate and salicylate transport in human red cells

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