Literature DB >> 5443167

Abnormal rheology of oxygenated blood in sickle cell anemia.

S Chien, S Usami, J F Bertles.   

Abstract

The viscosity of oxygenated blood from patients with sickle cell anemia (Hb SS disease) was found to be abnormally increased, a property which contrasts with the well recognized viscous aberration produced by deoxygenation of Hb SS blood. Experiments designed to explain this finding led to considerations of deformation and aggregation, primary determinants of the rheologic behavior of erythrocytes as they traverse the microcirculation. Deformability of erythrocytes is in turn dependent upon internal viscosity (i.e. the state and concentration of hemoglobin in solution) and membrane flexibility. Definition of the contribution made by each of these properties to the abnormal viscosity of oxygenated Hb SS blood was made possible by analysis of viscosity measurements, made over a wide range of shear rates and cell concentrations, on Hb SS erythrocytes and normal erythrocytes suspended in Ringer's solution (where aggregation does not occur) and in plasma. Similar measurements were made on the two cell types separated by ultracentrifugation of Hb SS erythrocytes: high density erythrocytes composed of 50 to 70% irreversibly "sickled" cells (ISC) and low density erythrocytes composed of over 95% non-ISC. Under all experimental conditions (hematocrit, shear rate, and suspending medium) the viscosity of ISC exceeds that of normal erythrocytes. The viscosity of non-ISC is elevated only in the absence of aggregation and over intermediate ranges of hematocrit. Analyses of the data reveal (a) an elevated internal viscosity of ISC: (b) a reduced membrane flexibility of both ISC and non-ISC, particularly at low shear rates; and (c) a reduced tendency for aggregation displayed by both cell types. The abnormal viscosity of oxygenated Hb SS blood can be attributed to the altered rheology of ISC and, to a lesser extent, of non-ISC. These studies assign a role to the abnormal rheology of Hb SS erythrocytes in the pathogenesis of sickle cell anemia, even under conditions of complete oxygenation.

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Year:  1970        PMID: 5443167      PMCID: PMC322516          DOI: 10.1172/JCI106273

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  35 in total

1.  HEMODILUTION, TONICITY, AND BLOOD VISCOSITY.

Authors:  P W RAND; E LACOMBE
Journal:  J Clin Invest       Date:  1964-11       Impact factor: 14.808

2.  EFFECT OF MEAN CORPUSCULAR HEMOGLOBIN CONCENTRATION ON VISCOSITY.

Authors:  A J ERSLEV; J ATWATER
Journal:  J Lab Clin Med       Date:  1963-09

3.  Paper electrophoresis of serum proteins in Cooley's anaemia and sickle cell anaemia.

Authors:  J ALLAMANIS
Journal:  Acta Paediatr       Date:  1955-03       Impact factor: 2.299

4.  Physical properties of red cells as related to effects in vivo. I. Increased rigidity of erythrocytes as measured by viscosity of cells altered by chemical fixation, sickling and hypertonicity.

Authors:  T H Ham; R F Dunn; R W Sayre; J R Murphy
Journal:  Blood       Date:  1968-12       Impact factor: 22.113

5.  Hemoglobin CC disease: rheological properties or erythrocytes and abnormalities in cell water.

Authors:  J R Murphy
Journal:  J Clin Invest       Date:  1968-07       Impact factor: 14.808

6.  Red blood cells: why or why not?

Authors:  K Schmidt-Nielsen; C R Taylor
Journal:  Science       Date:  1968-10-11       Impact factor: 47.728

7.  Plasma trapping in hematocrit determination. Differences among animal species.

Authors:  S Chien; R J Dellenback; S Usami; M I Gregersen
Journal:  Proc Soc Exp Biol Med       Date:  1965 Aug-Sep

8.  Effects of hematocrit and plasma proteins on human blood rheology at low shear rates.

Authors:  S Chien; S Usami; H M Taylor; J L Lundberg; M I Gregersen
Journal:  J Appl Physiol       Date:  1966-01       Impact factor: 3.531

9.  Theoretical considerations of the elasticity of red cells and small blood vessels.

Authors:  Y C Fung
Journal:  Fed Proc       Date:  1966 Nov-Dec

10.  Pathogenesis of hemolytic anemia in homozygous hemoglobin C disease.

Authors:  S Charache; C L Conley; D F Waugh; R J Ugoretz; J R Spurrell
Journal:  J Clin Invest       Date:  1967-11       Impact factor: 14.808

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  72 in total

1.  Influence of sickle hemoglobin polymerization and membrane properties on deformability of sickle erythrocytes in the microcirculation.

Authors:  C Dong; R S Chadwick; A N Schechter
Journal:  Biophys J       Date:  1992-09       Impact factor: 4.033

2.  Monovalent cation transport in irreversibly sickled cells.

Authors:  M R Clark; C E Morrison; S B Shohet
Journal:  J Clin Invest       Date:  1978-08       Impact factor: 14.808

3.  Dynamics of oxygen unloading from sickle erythrocytes.

Authors:  V B Makhijani; G R Cokelet; A Clark
Journal:  Biophys J       Date:  1990-10       Impact factor: 4.033

4.  Intermolecular interactions of oxygenated sickle hemoglobin molecules in cells and cell-free solutions.

Authors:  T R Lindstrom; S H Koenig; T Boussios; J F Bertles
Journal:  Biophys J       Date:  1976-06       Impact factor: 4.033

Review 5.  Physiological responses of sickle cell trait carriers during exercise.

Authors:  Philippe Connes; Harvey Reid; Marie-Dominique Hardy-Dessources; Errol Morrison; Olivier Hue
Journal:  Sports Med       Date:  2008       Impact factor: 11.136

6.  Hyperfibrinogenaemia and hyperviscosity in sickle-cell crisis.

Authors:  S G Richardson; G R Breeze; J Stuart
Journal:  J Clin Pathol       Date:  1976-10       Impact factor: 3.411

Review 7.  Pulmonary vascular resistance and viscosity: the forgotten factor.

Authors:  Julien I E Hoffman
Journal:  Pediatr Cardiol       Date:  2011-03-25       Impact factor: 1.655

Review 8.  Measuring success: utility of biomarkers in sickle cell disease clinical trials and care.

Authors:  Ram Kalpatthi; Enrico M Novelli
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

9.  Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells.

Authors:  S E Lux; K M John; M J Karnovsky
Journal:  J Clin Invest       Date:  1976-10       Impact factor: 14.808

10.  Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia.

Authors:  Clément Lemaire; Yann Lamarre; Nathalie Lemonne; Xavier Waltz; Sadri Chahed; Florence Cabot; Ioana Botez; Benoit Tressieres; Marie-Laure Lalanne-Mistrih; Maryse Etienne-Julan; Philippe Connes
Journal:  Clin Hemorheol Microcirc       Date:  2013-01-01       Impact factor: 2.375

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