Literature DB >> 7174796

SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequences.

M E Fabry, D K Kaul, C Raventos-Suarez, H Chang, R L Nagel.   

Abstract

We have examined 20 SC patients on Percoll-Stractan continuous density gradients and find that they have an elevated mean corpuscular hemoglobin concentration (MCHC). Reduction of the MCHC to normal values results in amelioration of four physiologically important blood abnormalities: decreased oxygen affinity, viscosity of deoxygenated erythrocyte suspensions, rate of sickling, and deoxygenation induced K+ efflux. These observations suggest that the rehydration of SC cells to normal values should be considered a potential approach in the therapeutic manipulation of this disease.

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Year:  1982        PMID: 7174796      PMCID: PMC370350          DOI: 10.1172/jci110732

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


  6 in total

1.  The effects of alkylureas and nitrogen mustards on the kinetics of red cell sickling.

Authors:  J P Harrington; R L Nagel
Journal:  J Lab Clin Med       Date:  1977-11

2.  A decreased effect of organic phosphates on hemoglobin S at low concentrations.

Authors:  Y Ueda; R M Bookchin; R L Nagel
Journal:  Biochem Biophys Res Commun       Date:  1978-11-29       Impact factor: 3.575

3.  Heterogeneity of red cells in the sickler: a characteristic with practical clinical and pathophysiological implications.

Authors:  M E Fabry; R L Nagel
Journal:  Blood Cells       Date:  1982

4.  The effects of sickling on ion transport. I. Effect of sickling on potassium transport.

Authors:  D C TOSTESON; E CARLSEN; E T DUNHAM
Journal:  J Gen Physiol       Date:  1955-09-20       Impact factor: 4.086

5.  Some aspects of the pathophysiology of homozygous Hb CC erythrocytes.

Authors:  M E Fabry; D K Kaul; C Raventos; S Baez; R Rieder; R L Nagel
Journal:  J Clin Invest       Date:  1981-05       Impact factor: 14.808

6.  pH dependency of potassium efflux from sickled red cells.

Authors:  E F Roth; R L Nagel; R M Bookchin
Journal:  Am J Hematol       Date:  1981       Impact factor: 10.047

  6 in total
  17 in total

1.  Hemoglobin sickle cell disease complications: a clinical study of 179 cases.

Authors:  François Lionnet; Nadjib Hammoudi; Katia Stankovic Stojanovic; Virginie Avellino; Gilles Grateau; Robert Girot; Jean-Philippe Haymann
Journal:  Haematologica       Date:  2012-02-07       Impact factor: 9.941

2.  Human bulbar conjunctival hemodynamics in hemoglobin SS and SC disease.

Authors:  Justin Wanek; Bruce Gaynes; Jennifer I Lim; Robert Molokie; Mahnaz Shahidi
Journal:  Am J Hematol       Date:  2013-06-12       Impact factor: 10.047

3.  Density-based separation in multiphase systems provides a simple method to identify sickle cell disease.

Authors:  Ashok A Kumar; Matthew R Patton; Jonathan W Hennek; Si Yi Ryan Lee; Gaetana D'Alesio-Spina; Xiaoxi Yang; Julie Kanter; Sergey S Shevkoplyas; Carlo Brugnara; George M Whitesides
Journal:  Proc Natl Acad Sci U S A       Date:  2014-09-02       Impact factor: 11.205

4.  Polymerization in erythrocytes containing S and non-S hemoglobins.

Authors:  C T Noguchi
Journal:  Biophys J       Date:  1984-06       Impact factor: 4.033

5.  Regulation of cation content and cell volume in hemoglobin erythrocytes from patients with homozygous hemoglobin C disease.

Authors:  C Brugnara; A S Kopin; H F Bunn; D C Tosteson
Journal:  J Clin Invest       Date:  1985-05       Impact factor: 14.808

6.  Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.

Authors:  C T Noguchi; D A Torchia; A N Schechter
Journal:  J Clin Invest       Date:  1983-09       Impact factor: 14.808

7.  Two cases of hematuria with hemoglobin C trait.

Authors:  John David Spencer; John T Sanders; Bettina H Ault
Journal:  Pediatr Nephrol       Date:  2009-08-11       Impact factor: 3.714

8.  Original Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease.

Authors:  Carly C Ginter Summarell; Vivien A Sheehan
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-17

9.  The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs.

Authors:  E A Rachmilewitz; H Tamari; F Liff; Y Ueda; R L Nagel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease.

Authors:  Julien Tripette; Tamas Alexy; Marie-Dominique Hardy-Dessources; Daniele Mougenel; Eric Beltan; Tawfik Chalabi; Roger Chout; Maryse Etienne-Julan; Olivier Hue; Herbert J Meiselman; Philippe Connes
Journal:  Haematologica       Date:  2009-08       Impact factor: 9.941

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