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Citations to this article

The Effects of Cyanate In Vitro on Red Blood Cell Metabolism and Function in Sickle Cell Anemia
Frank G. De Furia, … , Anthony Cerami, James M. Manning
Frank G. De Furia, … , Anthony Cerami, James M. Manning
Published March 1, 1972
Citation Information: J Clin Invest. 1972;51(3):566-574. https://doi.org/10.1172/JCI106845.
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The Effects of Cyanate In Vitro on Red Blood Cell Metabolism and Function in Sickle Cell Anemia

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Abstract

Cyanate, which is in equilibrium with urea, combines with the α-amino group of the aminoterminal valine of hemoglobin in an irreversible, specific carbamylation reaction. Partial carbamylation (0.72 residues/hemoglobin tetramer) as determined by cyanate-14C incorporation or hydantoin analysis diminishes the in vitro sickling phenomenon. Since cyanate may react not only with hemoglobin but also with functional groups of other red blood cell proteins, the in vitro effect of cyanate was studied on sickle cells. Cells were incubated with 10 mM KCl (control) or 10 mM KNCO (carbamylated) for 1 hr, washed, and resuspended in autologous plasma. Glycolysis, ATP and 2,3-diphosphoglyceric acid (DPG) stability, autohemolysis, and osmotic fragility were not affected by carbamylation. Potassium loss in carbamylated cells (2.8 mmol/liter) was less than in control cells (9.0 mmol/liter). Pyruvate kinase activity of carbamylated cells was decreased (∼25%) but the activities of other glycolytic enzymes were similar to those of control cells. Oxygen affinity of carbamylated sickle, normal, and DPG-depleted normal cells increased, and was a sensitive index of the degree and duration of reaction with cyanate. The reactivity of carbamylated cells to DPG was similar to control cells. DPG-depleted carbamylated cells regenerated DPG and increased the P50 when incubated with pyruvate, inosine, and phosphate. The Bohr effect of normal and of sickle cells was not affected (Δlog P50/Δ pH=-0.48 and -0.53, respectively) after carbamylation. The reserve buffering capacity of plasma offset the slightly diminished (∼15%) CO2 capacity of carbamylated cells so that whole blood CO2 capacity, pH, and PCO2 were normal. These studies provide further support for the potential clinical use of cyanate in treating and preventing the anemia and painful crises of sickle cell disease.

Authors

Frank G. De Furia, Denis R. Miller, Anthony Cerami, James M. Manning

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Year: 2022 2021 2017 2016 2015 2014 2011 2008 2006 2001 1999 1997 1996 1995 1994 1993 1990 1988 1987 1986 1983 1982 1981 1978 1977 1976 1975 1974 1973 1972 Total
Citations: 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 2 1 1 1 1 1 3 6 2 8 7 3 55
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Citations to this article (55)

Title and authors Publication Year
Avenues for post-translational protein modification prevention and therapy.
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Molecular Aspects of Medicine 2022
Phage-Display-Derived Peptide Specific to Carbamylated Protein
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ACS Omega 2021
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Longitudinal Changes in Protein Carbamylation and Mortality Risk after Initiation of Hemodialysis
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Cryobiology 1982
The Molecular Basis of Mutant Hemoglobin Dysfunction
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Erythrocyte Hb-S Concentration AN IMPORTANT FACTOR IN THE LOW OXYGEN AFFINITY OF BLOOD IN SICKLE CELL ANEMIA
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Journal of Clinical Investigation 1973
Effects of Cyanate and 2,3-Diphosphoglycerate on Sickling RELATIONSHIP TO OXYGENATION
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Sickle Cell Hemoglobin: Molecular Basis Of Sickling Phenomenon Theory And Therap
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1972

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