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      Red blood cell storage in additive solution-7 preserves energy and redox metabolism: a metabolomics approach

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          Abstract

          BACKGROUND

          Storage and transfusion of red blood cells (RBCs) has a huge medical and economic impact. Routine storage practices can be ameliorated through the implementation of novel additive solutions (ASs) that tackle the accumulation of biochemical and morphologic lesion during routine cold liquid storage in the blood bank, such as the recently introduced alkaline solution AS-7. Here we hypothesize that AS-7 might exert its beneficial effects through metabolic modulation during routine storage.

          STUDY DESIGN AND METHODS

          Apheresis RBCs were resuspended either in control AS-3 or experimental AS-7, before ultrahigh-performance liquid chromatography–mass spectrometry metabolomics analysis.

          RESULTS

          Unambiguous assignment and relative quantitation was achieved for 229 metabolites. AS-3 and AS-7 results in many similar metabolic trends over storage, with AS-7 RBCs being more metabolically active in the first storage week. AS-7 units had faster fueling of the pentose phosphate pathway, higher total glutathione pools, and increased flux through glycolysis as indicated by higher levels of pathway intermediates. Metabolite differences are especially observed at 7 days of storage, but were still maintained throughout 42 days.

          CONCLUSION

          AS-7 formulation (chloride free and bicarbonate loading) appears to improve energy and redox metabolism in stored RBCs in the early storage period, and the differences, though diminished, are still appreciable by Day 42. Energy metabolism and free fatty acids should be investigated as potentially important determinants for preservation of RBC structure and function. Future studies will be aimed at identifying metabolites that correlate with in vitro and in vivo circulation times.

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          Author and article information

          Journal
          0417360
          7833
          Transfusion
          Transfusion
          Transfusion
          0041-1132
          1537-2995
          23 January 2018
          14 August 2015
          December 2015
          22 February 2018
          : 55
          : 12
          : 2955-2966
          Affiliations
          [1 ]Department of Biochemistry and Molecular Genetics, University of Colorado Denver–Anschutz Medical Campus, Aurora, Colorado
          [2 ]Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire
          Author notes
          Address reprint requests to: Angelo D’Alessandro, Department of Biochemistry and Molecular Genetics, University of Colorado Denver Anschutz Medical Campus, Aurora, CO 80045; angelo.dalessandro@ 123456ucdenver.edu ; or Larry J. Dumont, Geisel School of Medicine at Dartmouth, One Medical Center Drive, Lebanon, NH 03756-0001; Larry.J.dumont@ 123456hitchcock.org
          Article
          PMC5823509 PMC5823509 5823509 nihpa936263
          10.1111/trf.13253
          5823509
          26271632
          874ea2f5-6390-457b-8465-52ccc6a0c62f
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