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Effects of glyceraldehyde on the structural and functional properties of sickle erythrocytes.
J Clin Invest. 1978 Jan; 61(1):11-9.JCI

Abstract

The d- and l-isomers of glyceraldehyde are equally effective in the inhibition of SS erythrocyte sickling in vitro. The following compounds at a concentration of 20 mM were ineffective in inhibiting sickling: glyceraldehyde-3-phosphate, d-erythrose, d-ribose, d-fructose, d-glucose, d-sucrose, dihydroxyacetone, and methylglyoxal. Glyceraldehyde does not reverse the sickling of cells in the deoxy state. The properties of purified hemoglobin after treatment with glyceraldehyde and of the hemoglobin isolated from treated cells are very similar; these results suggest that glyceraldehyde itself is the reactive species within the erythrocyte. Erythrocyte glutathione is decreased by treatment in vitro with the aldehyde. Relatively high concentrations of glyceraldehyde (50 mM) lead to a small amount (3%) of cross-linking between hemoglobin monomers as well as to some cross-linking of erythrocyte membrane proteins. Lower concentrations of dl-glyceraldehyde (5-20 mM), which reduce the sickling of erythrocytes in vitro, lead to proportionally less cross-linking of hemoglobin. Cells that have been treated with those concentrations of the aldehyde show little change in their osmotic fragility, exhibit improved filtration properties, and have a lowered viscosity.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

618907

Citation

Nigen, A M., and J M. Manning. "Effects of Glyceraldehyde On the Structural and Functional Properties of Sickle Erythrocytes." The Journal of Clinical Investigation, vol. 61, no. 1, 1978, pp. 11-9.
Nigen AM, Manning JM. Effects of glyceraldehyde on the structural and functional properties of sickle erythrocytes. J Clin Invest. 1978;61(1):11-9.
Nigen, A. M., & Manning, J. M. (1978). Effects of glyceraldehyde on the structural and functional properties of sickle erythrocytes. The Journal of Clinical Investigation, 61(1), 11-9.
Nigen AM, Manning JM. Effects of Glyceraldehyde On the Structural and Functional Properties of Sickle Erythrocytes. J Clin Invest. 1978;61(1):11-9. PubMed PMID: 618907.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Effects of glyceraldehyde on the structural and functional properties of sickle erythrocytes. AU - Nigen,A M, AU - Manning,J M, PY - 1978/1/1/pubmed PY - 1978/1/1/medline PY - 1978/1/1/entrez SP - 11 EP - 9 JF - The Journal of clinical investigation JO - J Clin Invest VL - 61 IS - 1 N2 - The d- and l-isomers of glyceraldehyde are equally effective in the inhibition of SS erythrocyte sickling in vitro. The following compounds at a concentration of 20 mM were ineffective in inhibiting sickling: glyceraldehyde-3-phosphate, d-erythrose, d-ribose, d-fructose, d-glucose, d-sucrose, dihydroxyacetone, and methylglyoxal. Glyceraldehyde does not reverse the sickling of cells in the deoxy state. The properties of purified hemoglobin after treatment with glyceraldehyde and of the hemoglobin isolated from treated cells are very similar; these results suggest that glyceraldehyde itself is the reactive species within the erythrocyte. Erythrocyte glutathione is decreased by treatment in vitro with the aldehyde. Relatively high concentrations of glyceraldehyde (50 mM) lead to a small amount (3%) of cross-linking between hemoglobin monomers as well as to some cross-linking of erythrocyte membrane proteins. Lower concentrations of dl-glyceraldehyde (5-20 mM), which reduce the sickling of erythrocytes in vitro, lead to proportionally less cross-linking of hemoglobin. Cells that have been treated with those concentrations of the aldehyde show little change in their osmotic fragility, exhibit improved filtration properties, and have a lowered viscosity. SN - 0021-9738 UR - https://www.unboundmedicine.com/medline/citation/618907/Effects_of_glyceraldehyde_on_the_structural_and_functional_properties_of_sickle_erythrocytes_ L2 - https://doi.org/10.1172/JCI108909 DB - PRIME DP - Unbound Medicine ER -