Effects of alkanols, alkanediols and glycerol on red blood cell shape and hemolysis

• Published in: Biochimica et biophysica acta 1996-04, Vol.1280 (1), p.73-80
• Main Authors: Bakaltcheva, Irina B., Odeyale, Charles O., Spargo, Barry J.
• Format: Article
• Language: English
• Subjects: Alcohols - pharmacology; Cell shape; Cryoprotectant toxicity; Dielectric constant; Erythrocyte; Erythrocyte Membrane - drug effects; Erythrocyte Membrane - physiology; Erythrocyte Membrane - ultrastructure; Erythrocytes - cytology; Erythrocytes - drug effects; Erythrocytes - physiology; Glycerol - pharmacology; Hemolysis; Hemolysis - drug effects; Humans; Kinetics; Mathematics; Partition coefficient; Polyol; Structure-Activity Relationship; Temperature
• ISSN: 0005-2736; 0006-3002; 1879-2642
• DOI: 10.1016/0005-2736(95)00279-0

The physicochemical effects of a series of alkanols, alkanediols and glycerol on erythrocyte shape and hemolysis at 4 and 20°C were examined. We calculated the dielectric constant of the incubation medium, D s, and the dielectric constant of the erythrocyte membrane D m in the presence of organic solutes. The ratio D s D m = −38.48 at 20°C defines the normal biconcave shape in a medium without hemolytic agents. A decrease in D s D m favors externalization or internalization with consequent hemolysis. Alkanols and alkanediols convert biconcave erythrocytes into echinocytes, which is accompanied by an increase in the projected surface area. Glycerol converts biconcave erythrocytes into stomatocytes, which was accompanied by a marginal decrease in the projected surface area. Progressive externalization in alkanols and alkanediols or internalization in glycerol resulted in a decrease in the projected surface area and the formation of smooth spheres. The degree of shape change induced was related to the degree of hemolysis and the ratio D s D m . A decrease in temperature reduced both the degree of shape change and hemolysis. Our results suggest that physicochemical toxicity may be a result of a temperature dependent hydrophobic interaction between the organic solutes and the membrane and is best interpreted by the ability of the solutes to change D s and D m. These results are discussed with respect to the physicochemical constants of the organic solutes.