1986
DOI: 10.1042/bj2370265
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Sickle cell membranes and oxidative damage

Abstract: Sickle erythrocytes and their membranes are susceptible to endogenous free-radical-mediated oxidative damage which correlates with the proportion of irreversibly sickled cells. The suppression of incubation-induced oxidative stress by antioxidants, free radical scavengers and an iron chelator suggest that oxidation products of membrane-bound haemoglobin contribute towards the pathology of the disease.

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Cited by 144 publications
(82 citation statements)
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References 36 publications
(33 reference statements)
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“…The action of DTT in vitro suggests that circulating sickle cells are already deprived of reduced thiols (Kamp et al , 2001). Indeed, sickle cells are reported to contain lower levels of membrane thiols (Rank et al , 1985; Rice‐Evans et al , 1986). HOCl also reacts with membrane thiols.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The action of DTT in vitro suggests that circulating sickle cells are already deprived of reduced thiols (Kamp et al , 2001). Indeed, sickle cells are reported to contain lower levels of membrane thiols (Rank et al , 1985; Rice‐Evans et al , 1986). HOCl also reacts with membrane thiols.…”
Section: Discussionmentioning
confidence: 99%
“…This is particularly significant in diseases such as SCA in which vascular oxidative stress is increased (Rice‐Evans et al , 1986) with accumulations of highly reactive oxygen species (ROS) including the superoxide anion, hydrogen peroxide and the hydroxyl radical (Sies, 1997; Chirico & Pialoux, 2012; Voskou et al , 2015). Myeloperoxidase released from activated neutrophils may also add to oxidant challenge in SCA, through production of hypochlorous acid (HOCl) from hydrogen peroxide (Vissers et al , 1994; Mutze et al , 2003; Zhang et al , 2013).…”
mentioning
confidence: 99%
“…[12] Specifically, sickle erythrocytes and their membranes are susceptible to endogenous free radical-mediated oxidative damage that correlates with the proportion of irreversibly sickled erythrocytes. [13] Furthermore, accumulation of hydrogen peroxide (H 2 O 2 ) decreases the half life of erythrocytes by increasing oxidation of polyunsaturated fatty acids of cell membrane [14] and can oxidize haemoglobin to methaemoglobin. [9,15] Methaemoglobin does not bind reversibly with oxygen.…”
Section: Introductionmentioning
confidence: 99%
“…Free radical action and lipid peroxidation have been suggested as potentially important causative agents of aging and several types of human diseases [24]. Reactive oxygen species (ROS) have been implicated in damage to erythrocytes in patients with β-thalassemia, sickle cell anemia, glucose-6-phosphate dehydrogenase deficiency and other hemoglobinopathies [25,26]. Aqueous extracts of Conyza canadensis interact in some way with the biological membranes.…”
Section: Resultsmentioning
confidence: 99%