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Acid Sphingomyelinase Inhibition Prevents Hemolysis During Erythrocyte Storage

Authors :
Richard S. Hoehn
Peter L. Jernigan
Alex L. Chang
Michael J. Edwards
Charles C. Caldwell
Erich Gulbins
Timothy A. Pritts
Source :
Cellular Physiology and Biochemistry, Vol 39, Iss 1, Pp 331-340 (2016)
Publication Year :
2016
Publisher :
Cell Physiol Biochem Press GmbH & Co KG, 2016.

Abstract

Background/Aims: During storage, units of human red blood cells (pRBCs) experience membrane destabilization and hemolysis which may cause harm to transfusion recipients. This study investigates whether inhibition of acid sphingomyelinase could stabilize erythrocyte membranes and prevent hemolysis during storage. Methods: Human and murine pRBCs were stored under standard blood banking conditions with and without the addition of amitriptyline, a known acid sphingomyelinase inhibitor. Hemoglobin was measured with an electronic hematology analyzer and flow cytometry was used to measure erythrocyte size, complexity, phosphatidylserine externalization, and band 3 protein expression. Results: Cell-free hemoglobin, a marker of hemolysis, increased during pRBC storage. Amitriptyline treatment decreased hemolysis in a dose-dependent manner. Standard pRBC storage led to loss of erythrocyte size and membrane complexity, increased phosphatidylserine externalization, and decreased band 3 protein integrity as determined by flow cytometry. Each of these changes was reduced by treatment with amitriptyline. Transfusion of amitriptyline-treated pRBCs resulted in decreased circulating free hemoglobin. Conclusion: Erythrocyte storage is associated with changes in cell size, complexity, membrane molecular composition, and increased hemolysis. Acid sphingomyelinase inhibition reduced these changes in a dose-dependent manner. Our data suggest a novel mechanism to attenuate the harmful effects after transfusion of aged blood products.

Details

Language :
English
ISSN :
10158987 and 14219778
Volume :
39
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Cellular Physiology and Biochemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.8cbd18c5cc6c4a41aaffb3d6ae24029a
Document Type :
article
Full Text :
https://doi.org/10.1159/000445627