4.7 Article

Blood donor exposome and impact of common drugs on red blood cell metabolism

Journal

JCI INSIGHT
Volume 6, Issue 3, Pages -

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/jci.insight.146175

Keywords

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Funding

  1. National Heart, Lung, and Blood Institute (NHL-BI) Recipient Epidemiology and Donor Evaluation Study-III (REDS-III)
  2. NHL-BI [HHSN2682011-00001I]
  3. National Institute of General and Medical Sciences [RM1GM131968]
  4. Boettcher Webb-Waring Investigator Award [R01HL146442, R01HL149714, R01HL148151, R21HL150032, T32 HL007171]
  5. NHLBI [12801, 303.724.0096]

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Computational models suggest that mature erythrocytes may be affected by common drugs. High-throughput drug screenings show that many drugs impact erythrocyte metabolism, with machine learning models accurately predicting these effects. Certain drugs like ranitidine can improve erythrocyte metabolism and storage quality, indicating potential for enhancing blood transfusion outcomes.
Computational models based on recent maps of the RBC proteome suggest that mature erythrocytes may harbor targets for common drugs. This prediction is relevant to RBC storage in the blood bank, in which the impact of small molecule drugs or other xenometabolites deriving from dietary, iatrogenic, or environmental exposures (exposome) may alter erythrocyte energy and redox metabolism and, in so doing, affect red cell storage quality and posttransfusion efficacy. To test this prediction, here we provide a comprehensive characterization of the blood donor exposome, including the detection of common prescription and over-the-counter drugs in blood units donated by 250 healthy volunteers in the Recipient Epidemiology and Donor Evaluation Study Ill Red Blood Cell-Omits (REDS-Ill RBC-Omics) Study. Based on high-throughput drug screenings of 1366 FDA-approved drugs, we report that approximately 65% of the tested drugs had an impact on erythrocyte metabolism. Machine learning models built using metabolites as predictors were able to accurately predict drugs for several drug classes/targets (bisphosphonates, anticholinergics, calcium channel blockers, adrenergics, proton pump inhibitors, antimetabolites, selective serotonin reuptake inhibitors, and mTOR), suggesting that these drugs have a direct, conserved, and substantial impact on erythrocyte metabolism. As a proof of principle, here we show that the antacid ranitidine - though rarely detected in the blood donor population - has a strong effect on RBC markers of storage quality in vitro. We thus show that supplementation of blood units stored in bags with ranitidine could - through mechanisms involving sphingosine 1-phosphate-dependent modulation of erythrocyte glycolys is and/or direct binding to hemoglobin - improve erythrocyte metabolism and storage quality.

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