1992
DOI: 10.1007/bf00249691
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Effect of Cu2+-ascorbic acid on lipid peroxidation, Mg2+-ATPase activity and spectrin of RBC membrane and reversal by erythropoietin

Abstract: The effect of erythropoietin (Ep), a glycoprotein hormone, has been studied on lipid peroxidation induced by Cu2+ and ascorbate in vitro, Mg2+ ATPase activity and spectrin of RBC membrane. Our present investigation reveals that Cu2+ and ascorbic acid increases lipid peroxidation of RBC membrane significantly. It has further been observed that under the same experimental condition spectrin, a major cytoskeleton membrane protein, and Mg(2+)-ATPase activity of RBC membrane decrease significantly. However, exogeno… Show more

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Cited by 18 publications
(8 citation statements)
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“…In an attempt to confirm whether melatonin directly scavenges · OH, an in vitro study was carried out using an established · OH generating system [36]. Fig.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In an attempt to confirm whether melatonin directly scavenges · OH, an in vitro study was carried out using an established · OH generating system [36]. Fig.…”
Section: Resultsmentioning
confidence: 99%
“…To examine whether melatonin scavenges · OH in an in vitro system, · OH were generated for 1 hr in a system containing sodium phosphate buffer (50 mM; pH 7.4), ascorbate (1 mM) and 0.2 mM Cu 2+ [36, 37] in the absence or presence of DMSO (500 μ M) and different concentrations of melatonin in a final volume of 1 mL. For melatonin experiments, controls with ethanol were always included as the solution was prepared in the presence of ethanol, which scavenges · OH.…”
Section: Methodsmentioning
confidence: 99%
“…For the preparation of hemoglobin-free ghosts, a method slightly modified from that of Dodge et al was followed [23][24][25]. Hemolysis of the washed red blood cells was performed in 5 mM sodium phosphate buffer (pH 8.0) and pellets were obtained by centrifugation at 13500 rpm for 30 min at 0-4 • C. This process was repeated five to seven times until the pellet became colorless.…”
Section: Preparation Of Rbc Ghost Membranesmentioning
confidence: 99%
“…The incubation mixture containing mitochondrial membrane protein (1.6 mg/ml), 50 mM potassium phosphate buffer (pH 7.4), and 0.2mM Cu2+ and 1 mM ascorbic acid in a final volume of 1.0 ml was incubated at 37°C in an incubator for 1 hour. The reaction was terminated by the addition of 40 μl of 35 mM EDTA (Chattopadhyay et al, 1992).…”
Section: Incubation Of Mitochondria With Copper-ascorbatementioning
confidence: 99%