Oxidative stress in erythrocytes of banked ABO blood

Objective: To understand the responses of A, B, and O blood groups to oxidative stress (OS) induced through storage. Methods: A, B, and O blood units were obtained from the blood bank at KIMS Hospital, Bangalore, and stored for 35 days at 4°C in citrate phosphate dextrose adenine-1 solution. Every f...

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Veröffentlicht in:Hematology (Luxembourg) 2016-11, Vol.21 (10), p.630-634
Hauptverfasser: Carl, Hsieh, Soumya, Ravikumar, Srinivas, Prabhu, Vani, Rajashekharaiah
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container_issue 10
container_start_page 630
container_title Hematology (Luxembourg)
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creator Carl, Hsieh
Soumya, Ravikumar
Srinivas, Prabhu
Vani, Rajashekharaiah
description Objective: To understand the responses of A, B, and O blood groups to oxidative stress (OS) induced through storage. Methods: A, B, and O blood units were obtained from the blood bank at KIMS Hospital, Bangalore, and stored for 35 days at 4°C in citrate phosphate dextrose adenine-1 solution. Every fifth day, hemoglobin (Hb) was assessed in whole blood and erythrocytes were isolated from each group. OS markers such as (i) antioxidant enzymes [superoxide dismutase and catalase] and superoxides were assessed in hemolysate; (ii) lipid peroxidation product - malondialdehyde (MDA) and protein oxidation products [protein carbonyls, advanced oxidation protein products (AOPP), and protein sulfhydryls] were assessed in membrane ghosts. Results: Antioxidant enzymes and Hb were similar in all groups. Superoxides increased in blood group O. MDA and AOPP differed between the groups, where levels in blood group O were lower than blood groups A and B. Sulfhydryls were maintained throughout storage. Discussion: The antioxidant defense in A, B, and O groups were similar as evident from our results of Hb, antioxidant enzymes and sulfhydryls. However, the response of blood group O diverged from that of A and B, substantiated by the results of MDA, AOPP, and superoxides. Thus blood group O endured oxidative insult more efficiently than A and B. This study forms the basis for future studies on erythrocyte membrane and exploring blood group O as a potential candidate for prolonging storage.
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Methods: A, B, and O blood units were obtained from the blood bank at KIMS Hospital, Bangalore, and stored for 35 days at 4°C in citrate phosphate dextrose adenine-1 solution. Every fifth day, hemoglobin (Hb) was assessed in whole blood and erythrocytes were isolated from each group. OS markers such as (i) antioxidant enzymes [superoxide dismutase and catalase] and superoxides were assessed in hemolysate; (ii) lipid peroxidation product - malondialdehyde (MDA) and protein oxidation products [protein carbonyls, advanced oxidation protein products (AOPP), and protein sulfhydryls] were assessed in membrane ghosts. Results: Antioxidant enzymes and Hb were similar in all groups. Superoxides increased in blood group O. MDA and AOPP differed between the groups, where levels in blood group O were lower than blood groups A and B. Sulfhydryls were maintained throughout storage. Discussion: The antioxidant defense in A, B, and O groups were similar as evident from our results of Hb, antioxidant enzymes and sulfhydryls. However, the response of blood group O diverged from that of A and B, substantiated by the results of MDA, AOPP, and superoxides. Thus blood group O endured oxidative insult more efficiently than A and B. 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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects ABO blood
ABO Blood-Group System - metabolism
Adult
Antioxidant enzymes
Blood Banks
Blood Preservation
Erythrocytes
Erythrocytes - metabolism
Female
Humans
Male
Middle Aged
Oxidative stress
Oxidative Stress - physiology
Storage
Young Adult
title Oxidative stress in erythrocytes of banked ABO blood
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