Effect of Radiologic Contrast Media on Cell Volume Regulatory Mechanisms in Human Red Blood Cells

Abstract

Rationale and Objectives The authors performed this study to evaluate cell volume regulation in human red blood cells (RBCs) after incubation in solutions of three contrast media: iohexol (830 mOsm), ioxaglate (520 mOsm), and iodixanol (300 mOsm). Materials and Methods Whole blood sampled from six healthy subjects was exposed to Ringer solutions containing 25% or 5% vol/vol iohexol (final osmolality, 440 or 340 mOsm, respectively), ioxaglate (final osmolality, 395 or 335 mOsm, respectively), iodixanol (final osmolality, 330 or 315 mOsm, respectively), or NaCl (control solutions with the same osmolality as that of the contrast media). In some experiments, control RBCs were subjected to a hyposmotic solution (100 mOsm). RBC volumes were obtained with a Coulter counter. Results The RBCs showed normal regulatory cell shrinkage after hyposmotically induced swelling. All 25% vol/vol contrast material solutions and their control solutions induced RBC shrinkage (range, 6% ± 1 [standard error] to 22% ± 3). The same was true for cells exposed to 5% vol/vol contrast material (range, 4% ± 1 to 7% ± 1). The shrinkage phase was followed by cell swelling (10% ± 2 to 20% ± 2 for 25% contrast material and their control solutions and 8% ± 1 to 15% ± 2 for 5% contrast material and their control solutions). No contrast material–exposed RBCs increased their volumes to the level reached with their control solutions. Conclusion RBCs exposed to hyperosmotic iohexol, ioxaglate, or iodixanol solutions shrank and then swelled. The degree of shrinkage and subsequent swelling could not be explained simply with the osmolality of the test solutions. Physicochemical properties of the contrast media must be involved, putatively affecting electrolyte fluxes over the RBC membrane. Possible targets of these effects are the K +/Cl − symporter, K + channels, and the Na +/K +/Cl − symporter.